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Article

Blockade of Glycosphingolipid Synthesis Inhibits Cell Cycle and Spheroid Growth of Colon Cancer Cells In Vitro and Experimental Colon Cancer Incidence In Vivo

by
Richard Jennemann
1,*,
Martina Volz
1,
Felix Bestvater
2,
Claudia Schmidt
2,
Karsten Richter
3,
Sylvia Kaden
3,
Johannes Müthing
4,
Hermann-Josef Gröne
5,6,† and
Roger Sandhoff
1,†
1
Lipid Pathobiochemistry Group, German Cancer Research Center, 69120 Heidelberg, Germany
2
Light Microscopy Facility, German Cancer Research Center, 69120 Heidelberg, Germany
3
Core Facility Electron Microscopy, German Cancer Research Center, 69120 Heidelberg, Germany
4
Institute for Hygiene, University of Münster, 48149 Münster, Germany
5
Medical Faculty, University of Heidelberg, 69120 Heidelberg, Germany
6
Institute of Pharmacology, University of Marburg, 35043 Marburg, Germany
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2021, 22(19), 10539; https://doi.org/10.3390/ijms221910539
Submission received: 31 August 2021 / Revised: 21 September 2021 / Accepted: 22 September 2021 / Published: 29 September 2021
(This article belongs to the Special Issue Activity, Function and Druggability of Cancer-Related Enzymes)
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Abstract

:
Colorectal cancer (CRC) is one of the most frequently diagnosed cancers in humans. At early stages CRC is treated by surgery and at advanced stages combined with chemotherapy. We examined here the potential effect of glucosylceramide synthase (GCS)-inhibition on CRC biology. GCS is the rate-limiting enzyme in the glycosphingolipid (GSL)-biosynthesis pathway and overexpressed in many human tumors. We suppressed GSL-biosynthesis using the GCS inhibitor Genz-123346 (Genz), NB-DNJ (Miglustat) or by genetic targeting of the GCS-encoding gene UDP-glucose-ceramide-glucosyltransferase- (UGCG). GCS-inhibition or GSL-depletion led to a marked arrest of the cell cycle in Lovo cells. UGCG silencing strongly also inhibited tumor spheroid growth in Lovo cells and moderately in HCT116 cells. MS/MS analysis demonstrated markedly elevated levels of sphingomyelin (SM) and phosphatidylcholine (PC) that occurred in a Genz-concentration dependent manner. Ultrastructural analysis of Genz-treated cells indicated multi-lamellar lipid storage in vesicular compartments. In mice, Genz lowered the incidence of experimentally induced colorectal tumors and in particular the growth of colorectal adenomas. These results highlight the potential for GCS-based inhibition in the treatment of CRC.

1. Introduction

Colorectal cancer (CRC) is one of the most commonly diagnosed malignant cancers and the most common cancer of the gastrointestinal tract in humans [1]. Intestinal adenomas are benign polyps of the colon mucosa with the potential to mutate into cancerous lesions [2]. Certain risk factors foster the emergence of colorectal carcinomas. The majority of CRC occur in patients over 50 years of age. Excessive consumption of alcohol, nicotine abuse, consumption of red meat, and obesity are each associated with the prevalence of colorectal tumors [3,4]. Chronic colonic inflammation such as ulcerative colitis has also been linked to the development of cancer. Approximately 30% of CRC exhibit increased familial risk, due to inherited genetic polymorphisms [5].
Surgery is the treatment of choice for CRC at stages I-II and is paired with chemotherapy for the treatment of stages III-IV [6]. However, chemotherapy is frequently accompanied by drug resistance limiting its therapeutic success [7].
In search for an alternative or additional treatment strategy, we focused on the potential impact of a reduction of glycosphingolipid (GSL)-synthesis on CRC biology using in vitro and in vivo models. In a previous study we showed that the incidence of chemically induced hepatocellular carcinoma was markedly inhibited in mice after genetic deletion of hepatocyte specific UDP-glucose-ceramide-glucosyltransferase (Ugcg) [8].
The basic GSL, glucosylceramide (GlcCer), is synthesized from UDP-glucose and ceramide (Cer) at the cytosolic surface of the Golgi apparatus [9]. Glucosylceramide synthase (GCS) is encoded by the gene Ugcg in rodents and UGCG in humans and represents the rate limiting enzyme catalyzing the first step in the GSL-biosynthesis pathway (Figure 1A). GlcCer can be elongated after transition to the Golgi lumen by the addition of additional carbohydrates leading toward complex GSL-series and gangliosides (Figure 1A). GSLs are then shuttled to the plasma membrane where they are involved in processes such as cell adhesion, membrane receptor activation, signaling and endocytosis [10,11]. Interference in these cellular processes can influence cell proliferation, differentiation, migration, and survival. Silencing of GCS may thus interfere with cancer cell growth as shown in in vitro cell culture experiments and xenograft cancer models [12,13,14,15,16,17].
We show here that that inhibition of GSL-synthesis with N-[(1R,2R)-1-(2,3-dihy- dro-1,4-benzodioxin-6-yl)-1-hydroxy-3-pyrrolidin-1-ylpropan-2-yl]nonanamide (Genz- 123346 or Genz), n-butyl-deoxynojirimycin (NB-DNJ) (Miglustat) and by targeting UGCG with specific guide RNA by Crispr/Cas9 technology suppressed cell proliferation and tumor spheroid growth in Lovo and HCT116 human colon carcinoma cells in vitro. Using an experimental mouse cancer model mimicking many features of human CRC [18], tumor incidence in Genz-treated mice was shown to be significantly lower than in non-treated controls.

2. Results

2.1. Gene Expression Analysis of UGCG in Human Colorectal Adenocarcinomas

GCS the basic enzyme in the GSL-biosynthesis pathway (Figure 1A) is overexpressed in multiple human cancers including hepatocellular carcinoma, breast, cervix, non-small-cell lung cancer, and papillary thyroid carcinoma [8,19,20,21], and also in many cancer cell lines [22]. UGCG expression data from human colorectal adenocarcinomas suggested a lower expression in tumor as compared to normal colon tissue (Figure 1B). Importantly, the overall survival time of patients with high UGCG expression in tumors decreased significantly as compared to patients with low UGCG expression (Figure 1C) suggesting a potential impact of UGCG expression on cancer prognosis and patient survival. Data were evaluated using the gene expression profiling interactive analysis tool GEPIA (http://gepia.cancer-pku.cn/index.html accessed on 16 December 2020).

2.2. Treatment of Colon Carcinoma Cells with the GCS Inhibitor Genz Leads to Depletion of GSLs and to an Arrest of the Cell Cycle

We investigated the effects of lowering sphingolipid synthesis using the GCS inhibitor Genz (Figure 2A) on human Lovo- and HCT116 colon-carcinoma cell lines on cell proliferation. Both cell lines expressed predominantly neutral GSLs but their patterns differed markedly (Figure 2B,C). Untreated Lovo cells lacked globo-series GSLs (Figure 2D) and as judged from their migration on thin layer chromatography (TLC)-plates (Figure 2B). MS2 analysis further showed expression of GSLs of the lacto-series, i.e., Lc4Cer, Lc5Cer and Lewisa (fucosylated Lc4Cer, (Figures S1 and S2)). (GSLs are abbreviated according to the joint commission on biochemical nomenclature of glycolipids [23]). HCT116 cells in contrast expressed predominantly Gb3Cer and Gb4Cer, GSLs of the globo-series (Figure 2C). HCT116 cells showed low content of acidic GSLs, principally co-migrating with the gangliosides GM3 and GD3 (Figure 2C). GSLs significantly decreased in both cell lines following treatment with 1 and 5 µM Genz seen after four days (Figure 2B,C and Figure S3). A residual amount of neutral GSLs migrating on the level of HexCer remained in both cell lines likely consisting of GalCer whose synthesis is not effected by GCS inhibition (see also Figure S6). Treatment of Lovo cells with 1 µM and 5 µM Genz caused an arrest in the cell cycle (Figure 2E,F, quantification). An elevated number of Genz-treated cells arrested in G0/G1 phase whereas cell numbers in S and G2/M phase decreased as compared to untreated control cells. Only Genz-concentrations of 5 µM or above markedly inhibited the cell cycle of HCT116 cells (Figure 2G,H, quantification). Genz treatment did not alter cell viability of both cell lines (Figure S4A).
Genz treated cells were quantified after 4 days of culture and effects were further investigated using three-dimensional tumor spheroid cultures. The number of Lovo and HCT116 cells markedly decreased upon treatment (Figure S4B). Treatment with Genz also led to a reduction in tumor microsphere size of both Lovo- (Figure 2I,J, quantification) and HCT116 cells (Figure 2K,L, quantification).

2.3. UGCG-Inhibition by NB-DNJ (Miglustat) Also Affects Cell Cycle and Tumor Spheroid Growth of Lovo and HCT116 Cells

The iminosugar Miglustat (Figure 3A) at a concentration of 100 µM led to an almost complete GSL-depletion in Lovo (Figure 3B) and HCT116 cells (Figure 3C) after four days of culture.
Miglustat inhibited the cell cycle of Lovo cells in a manner similar to that seen with Genz (Figure 3D,E, quantification) but did not appear to impair the cell cycle of HCT116 cells (Figure 3F,G, quantification). Miglustat-treatment markedly inhibited tumor spheroid growth by both Lovo- (Figure 3H,I, quantification) and HCT116 cells (Figure 3J,K, quantification). The effects were small but significant after 6 days of culture but resulted in a highly relevant reduced sphere growth after 9 days of culture.

2.4. UGCG-Gene Deletion by Crispr/Cas9 Technology

Lovo- and HCT116 cells were targeted with UGCG-guide-RNA (gRNA) to help validate whether the cell cycle arrest seen, particularly observed in Lovo cells, could be assigned to the GCS-inhibition with Genz and Miglustat or occurred due to a secondary effect of the drugs. GSLs were successfully depleted in both cell lines (Figure 4A,D).
A double band in the extracts of both cell lines migrating at the height of HexCer remained in both UGCG-gRNA-treated cell lines. A perborate separation of GlcCer from GalCer on TLC indicated the presence of GalCer (Figure S5). An additional double band remained in UGCG-depleted HCT116 cells migrating at the height of lactosylceramide (LacCer). This compound likely consists of galabiosylceramide, which in similar manner as seen with GalCer was not targeted by UGCG-gRNA. We further investigated whether genetic GSL-depletion would lead to a comparable arrest of the cell cycle as seen with inhibitor treatment. We could not detect increased numbers of cells in GO/G1 phase or a reduction of cells in the S or G2/M phase of the cell cycle in UGCG-depleted HCT116 cells (Figure 4B,C, quantification). This finding is in general agreement with the data obtained from the 1 µM Genz and Miglustat treatment (Figure 2G,H and Figure 3F,G). Lovo cells in contrast showed a moderate arrest of the cell cycle upon UGCG depletion (Figure 4E,G, quantification) with elevated numbers of cells seen in GO/G1 phase and lower numbers in S- and G2/M phase. Inhibition of the cell cycle appeared slightly stronger in cells treated with 5 µM Genz (Figure 4F,G, quantification) than seen in the genetically modified cells, suggesting an additional Genz-associated contribution.

2.5. Treatment of Lovo and HCT116 Cells with Genz Causes Lipid Accumulation in Multivesicular Bodies (MVBs)

Ultrastructural investigation of Genz-treated cells by electron microscopy (EM) showed a dose-dependent increase in numbers of MVBs.
In this respect, the sensitivity of Lovo-cells appeared much higher as compared to HCT116-cells: While the increase in MVB-numbers was seen in Lovo-cultures at low 1 µM Genz treatment, HCT116-cells required higher doses (Figure 5A). The ultrastructure of membrane-organization also differed (Figure 5B,C). MVBs in HCT116-cells display strange corner shapes (Figure 5C). In both cell-lines vesicles inside MVBs exhibit multilamellar composition with potential of membranes to anneal into close stacks (Figure 5C and Figure S6). The number of abnormal structured multilamellar and lipid rich MVBs rose with increased Genz concentrations (Figure 5D). Our results are in agreement with a recent paper reporting elevated sphingomyelin storage in lysosomal compartments of cells treated with the GCS inhibitor PDMP [24]. The periodic repeat in those areas accounts for a membrane thickness of 3.8 to 4 nm. Analysis at optical definition to resolve the bi-layer of membranes suggested the presence of blunt ends, micellar convolutions as well as widening of the expectedly lipophilic inner leaflet suggesting perturbation of canonical unit-membrane organization (Figure S6). The alterations in vesicles detected by electron microscopy coincided with increased expression of the autophagy marker Lc3-II at elevated Genz-concentrations in both Lovo and HCT116 cells (Figure 5E,F).

2.6. GSL-Synthesis Inhibition by Miglustat or Ugcg-gRNA Did Not Cause Intra-Lysosomal Lipid Accumulation

In contrast to the Genz-treated cells, a lysosomal accumulation of lipids was not observed upon Miglustat- (Figure S7A,B) or Ugcg-gRNA treatment (Figure S7C,D) of Lovo- (Figure S7A,C) and HCT116 cells (Figure S7B,D).

2.7. MS2 Analysis of Colon Carcinoma Cells Indicated a Marked Sphingomyelin Increase upon GCS-Inhibitor Treatment

Mass-spec analysis of Genz-, Miglustat- and UGCG-gRNA- treated Lovo- and HCT116 cells was performed to identify specific effects on sphingolipid synthesis. The levels of HexCer in Lovo and HCT116 cells decreased to a similar extent independent of the method of GCS-silencing (Figure 6A–D). Sphingomyelin (SM)- and phosphatidylcholine (PC) content in Genz-treated Lovo (Figure 6A) and HCT116 cells (Figure 6B) increased as compared to controls. The SM and PC content rose with elevated Genz concentrations and was much higher as in gRNA-treated cells. Ceramide levels however did not appreciably change and were even slightly lower in UGCG-gRNA treated cells as compared to controls (Figure 6A,B).
Lovo- and HCT116 cells treated with Miglustat also showed elevated SM content as compared to controls (Figure 6C,D). The absolute increase was not as prominent as that seen in cells treated with Genz. PC increased only slightly in Lovo cells but not in HCT116 cells (Figure 6C). Miglustat application did not alter ceramide content of Lovo and HCT116 cells (Figure 6C,D).

2.8. Genz Treatment of Mice Lowers Incidence of Experimental Induced CRC

We then sought to validate these in vitro findings using a mouse model of experimental CRC. Colorectal tumors were induced with azoxymethane (AOM) in mice at the age of 8 to 10 weeks (Figure 7A). One week later, mice received dextrane sulfate (DSS) for five consecutive days. Mice received food either with or without Genz supplementation five weeks after tumor induction (Figure 7A). All animals were sacrificed fifteen weeks after CRC induction and tumor load and size were evaluated. Human colorectal tumors predominantly occur in regions of the sigmoid colon and the rectum [25,26] (Figure 7B). In the AOM/DSS model used here, Genz- and chow-fed animals developed tumors particularly in the rectal part of the colon (Figure 7B). Both number and size of the tumors treated with Genz were reduced (Figure 7C). The overall tumor number following Genz treatment was significantly lower as compared to control mice (5.10 ± 0.99 vs. 10.29 ± 1.29; p < 0.01). A reduction was observed for tumors smaller and larger than 2 mm in diameter (2.80 ± 0.51 vs. 5.00 ± 0.59 for tumors < 2 mm; p < 0.05 and 2.30 ± 0.70 vs. 5.29 ± 0.99 for tumors > 2 mm; p < 0.05). The mean tumor diameter of all tumors per mouse was smaller in the Genz-treated cohort as compared to tumors grown in colons of control mice (1.7 ± 0.2 mm vs. 2.1 ± 0.1 mm; p < 0.05) (Figure 7D). A total of 80.7% of the tumors from the Genz-treated mice and 89.1% of the tumors that developed in chow fed animals localized at the distal part of the colon, preferentially in the rectum and close to the anus (Figure 7B,C). A lower number of tumors grew in the medial part (colon transversum) of the colons of both cohorts. Tumors were almost absent in the proximal part (colon ascendum). All mice developed predominantly colorectal adenomas with markedly lower numbers upon Genz-feeding (Figure 8A,B). Ki67-positive cells were determined to elucidate a potential effect of Genz treatment on the proliferation of cells in crypts. Control mice contained a mean of 19.6 ± 0.24 and Genz fed animals 17.8 ± 0.22 (p < 0.001) Ki67-positive cells in tumor-free colon crypts (Figure 8C) suggesting an effect on cell division of highly proliferative cells.
Immunohistochemistry of the colon sections for F4/80+ cells indicated the presence of macrophages preferentially in the periphery of the tumor of both cohorts. Limited macrophages were seen to penetrate into the tumor (Figure 8D, left panel). Differences between Genz-treated mice and controls were not detectable. Very low numbers of T-cells could be detected with anti-CD3 antibodies (Figure 8D, middle panel). The number of TUNEL-positive, apoptotic cells in tumors did not differ between Genz-treated mice and controls (Figure 8D, right panel). The majority of these cells contained smaller nuclei and therefore could be distinguished from epithelial cells.

2.9. GSLs Are Reduced and SM Levels Elevated in the Intestine upon Genz-Feeding

Sphingolipid analysis by TLC and MS2 was then performed to elucidate potential alterations in sphingolipid content due to the Genz treatment of the mice. GlcCer and Gg4Cer (GA1) were the two major components detected in the intestine of adult mice (Figure 9A) [27]. The ratio between HexCer and GA1 was determined to be approximately 1:0.4. GM3 was only found within the acidic GSL-fraction in low concentrations (Figure 9A). MS2 analysis showed a reduction, particularly of the NS-, AS-, and to a lesser extent, AP-containing GSL-species in Genz-treated mice (Figure 9B,C). Although NS-, AS- and AP-species GSLs decreased, surprisingly, NP-Cer-levels were found to be markedly elevated (Figure 9D). Within SM, the NS-species increased upon Genz feeding (Figure 9E). TLC-analysis from heart, spleen, kidney, and liver indicated a strong decrease of GSLs in those organs upon Genz treatment (Figure S8A,B, quantification). Genz-feeding of mice only magically influenced their blood chemistry as compared to the chow cohort (Figure S9).

3. Discussion

To evaluate an alternative treatment of CRC we investigated the impact of GCS-silencing on cell cycle and tumor spheroid growth in vitro in Lovo and HCT116 human colon carcinoma cells. The potential of the GCS inhibitor Genz-123346 in an endogenous animal model of CRC was further validated in vivo. Lovo cells showed cell cycle arrest upon GCS-inhibition, which was similar in both the genetically modified- and inhibitor-treated cells suggesting an impact of GSLs on cell division. GSL-synthesis inhibition did not appear to strongly affect the cell cycle in HCT116 cells. Although 1 µM Genz in the culture medium led to almost a complete depletion of GSLs in treated cells, the cell cycle was more inhibited at elevated doses of 5 µM Genz and higher. Increased Genz concentrations suggested additional effects beyond silencing of GCS in HCT116 cells. In order to investigate the effect of Genz on CRC cells over a longer time, we monitored the growth of tumor microspheres in a three dimensional system. Both HCT116 and Lovo cells showed decreased tumor microsphere growth with pronounced growth retardation of Lovo cell spheroids at low concentrations of Genz or Miglustat.
Our results obtained from the GCS-inhibition in colon carcinoma cells were in agreement with findings from other malignant cancer cells in vitro. A series of studies have suggested that GCS silencing with GCS inhibitors could potentially alter the growth of melanoma [16,28], brain cancer [17,29], lung carcinoma [30], myeloid leukemia [14], hepatocellular carcinoma [8], and myeloma cells [31]. In these studies, either synthetic ceramide analogs such as d-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) and (D,L)-threo-1-phenyl-2-hexadecanoylamino-3-pyrrolidino-1-propanol (PPPP), or imino sugars such as Miglustat (NB-DNJ), and N-pentyl deoxyidonojirimycin (NP-DIJ; OGT2378) were used to inhibit GCS.
GCS inhibition has been associated with an accumulation of ceramides. Ceramides may foster apoptosis [32] and thereby affect tumor growth. Markedly elevated ceramide levels, however, were not observed here either the Lovo or HCT116 cells upon inhibitor treatment. Therefore, ceramides can be largely excluded as candidates for the cell cycle inhibition and tumor microsphere growth seen in these cells. A marked elevation of SM and PC in was observed in Lovo cells treated with Miglustat which was higher than that seen in either Lovo or HCT116 cells upon Genz treatment. The levels of SM and PC, however, far exceeded the levels of those lipids found in UGCG-gRNA-treated cells implying the presence of additional targets of the inhibitors, in particular of Genz, in the context of sphingolipid metabolism. As shown by electron microscopy, lipids in Genz-treated cells accumulated in lysosomes in multilayered, partly compacted- onion-like membrane fashion.
Normally sphingolipids and phospholipids are enzymatically degraded in lysosomal compartments. Acidic pH conditions are required for this process in order to avoid accumulation. Reports suggest that cationic amphiphilic drugs (CADs) may interfere with a regular catabolism of those lipids leading to severe lipid storage in lamellar structures in endolysosomes [33,34]. CADs are small molecules consisting of a hydrophobic tail with one or more aromatic rings and a hydrophilic amine, which can be protonated in lysosomes. Positively charged CADs interfere with the negatively charge found in intra-lysosomal vesicles required for lysosomal enzyme stabilization and regular lipid degradation [33,34]. Thereby, CADs are thought to influence the catalytic degradation of lipids such as SM by acidic sphingomyelinase, which needs an acidic milieu for proper activity [34,35]. The GCS inhibitor Genz fulfills the general structural properties of such a drug (Figure 2A) and may thus help explain the elevated lipid storage seen in lysosomes. This effect may help contribute to the GSL-depletion seen and influence the cell cycle. A similar accumulation of SM had recently been reported for HeLa cells treated with the GCS inhibitor PDMP [24] that displays similar relevant structural features as seen in Genz. Epidemiologic studies have highlighted a positive anti-cancer effect of CADs. Patients who had received CAD-based tricyclic antidepressants and -antihistamines before cancer diagnosis showed improved survival [36,37,38,39,40,41]. In support of these epidemiological studies in humans, antidepressants which selectively inhibit the reuptake of serotonin (SSRIs) such as citalopram, escitalopram, fluoxetine, and sertraline, which all are considered CADs, have been described in animal models to inhibit the growth of colon, prostate, and lung cancers as well as gliomas and melanomas [34]. Interestingly, CADs have also been described to induce a reversal of the multidrug resistance (MDR) as demonstrated in various murine cancer models [34]. MDR is one of the major pitfalls that occurs during chemotherapeutic treatment of CRC [7]. GCS elevation in cancer has been correlated with drug resistance [22,42,43,44]. GCS up- or down-regulation has been shown to influence expression of the multidrug resistance protein 1 (MDRI) that fosters resistance to many chemical drugs [45,46,47]. Thus, lowering of GCS could potentially enhance drug sensitivity in tumors [48,49,50] and thus help overcome chemoresistance [51,52,53,54,55,56]. GCS inhibitors such as Genz can substantially interfere with GSL-synthesis and through CAD-actions may help limit MDR.
Building upon our in vitro data and previous animal studies with selective CADs, we investigated the impact of the GCS inhibitor Genz on CRC growth in a spontaneous CRC mouse model. The chemical agent AOM was used to initiate colon cancer. AOM induces DNA alkylation which facilitates genomic mutations leading to cancer [57]. Mice additionally received DSS, which promoted cancer development by inducing colitis. Animals of the two cohorts, chow fed and Genz-treated mice developed particularly adenomas. However, we found a marked reduced incidence and smaller tumors in mice treated with the GCS inhibitor and cationic amphiphilic drug Genz. We detected reduced GSL- and elevated SM-levels in the intestine of Genz-treated animals, but the changes were not as much pronounced as in the in vitro cell culture studies. However, a reduced number of Ki67-positive cells in the crypts of mouse colons indicated an effect of Genz on proliferative cells. The differences between treated and non-treated mice were faint, but distinct, and could help explain the reduced tumor numbers and size of tumors that developed over an extended period of time. Importantly, GCS inhibitors have been used successfully in preclinical studies to reduce substrate in GSL-storage disease patients such as Fabry and Gaucher disease [58,59].
Although the exact molecular mechanisms of the Genz-dependent decrease of the tumor incidence in the CRC-model need to be further elucidated, the use of GCS inhibitors in the treatment of human colorectal cancer may represent a novel therapeutic approach.

4. Materials and Methods

4.1. Validation of the UGCG Expression in Human CRC and UGCG-Related Survival

UGCG gene expression analysis of human colorectal adenocarcinomas and survival time of patients with high and low UGCG expression in tumors was performed using the TCGA normal and GTEx database in the gene expression profiling interactive analysis tool GEPIA (http://gepia.cancer-pku.cn/index.html, accessed on 16 December 2020).

4.2. GCS Silencing of Lovo and HCT116 Cells with Chemical Inhibitors

Lovo and HCT116 cells (ATCC, Manassas, VA, USA) were cultivated in MEM-alpha medium (Sigma, Munich, Germany), supplemented with 10% FCS, 2 mM L-glutamine, and 50 units/mL each of Pen/Strep (all from Life Technologies, Darmstadt, Germany) at 37 °C and 5% CO2 atmosphere. 2 × 105 cells each were cultivated in 10 mL culture medium in- or without the presence of the indicated concentrations of Genz-123346 (N-[(1R,2R)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-hydroxy-3-pyrrolidin-1-ylpropan-2-yl]nonanamide) (Chess, Mannheim, Germany) or with 100 µM NB-DNJ (Miglustat, Biozol, Eching, Germany). Cells were cultivated in 10 cm tissue culture dishes (Greiner Bio One, Frickenhausen, Germany) for 4 days. Cells were counted, split and 106 cells treated for another 2 days, each in triplicates. Cells were harvested and used for FACS-, protein-, and TLC-analysis.

4.3. UGCG Deletion in Lovo Colon Carcinoma Cells Using CRISPR/Cas9 Technology

A CRISPR/Cas9 expression vector with puromycin and ampicillin resistance (pX459, Addgene, Cambridge, MA, USA) was used for integration of the human UGCG-gRNA. The vector (5 µg) was digested with 10 units of the enzyme Bbs I (Thermo Scientific, Waltham, MA, USA) at 37 °C for 16 h. The DNA was purified using a PCR-purification Kit (Qiagen, Hilden, Germany).
The guide oligos including the 5′- and 3′-Bbs I overhangs, respectively were:
UGCG-guide-119 forward: 5′-caccgcgattacacctcaacaaga-3′;
UGCG-guide-119 reverse: 5′-aaactcttgttgaggtgtaatcgc-3′.
UGCG-guide-451 forward: 5′-caccgccatgtcagtaagcgtatc-3′;
UGCG-guide-451 reverse: 5′-aaacgatacgcttactgacatggc-3′.
Guide oligos, were dissolved at a concentration of 150 µM. 25 µL of the respective forward and reverse oligonucleotides were mixed and annealed (95 °C, 4′; 70 °C, 10′; followed by cooling down the mixture in a thermomixer (Eppendorf, Hamburg, Germany) to room temperature. For oligo insertion, ~100 ng of the purified expression vector, 1 ng of the annealed oligo and 1 unit of T4-ligase and ligase buffer (Life Technologies, Darmstadt, Germany) in a total volume of 20 µL (ad. ddH2O) were used. DH5α E. coli (Life Technologies, Darmstadt, Germany) were transformed with 5 µL of the ligation mixtures according to the manufacturer’s protocol and spread on LB agar gel plates with 100 µg/mL ampicillin. The plates were incubated at 37 °C for 16 h. Minipreps of single colonies were performed in 5 mL LB medium with 100 µg/mL ampicillin at 37 °C in a bacteria shaker for 16 h. The plasmid DNA was isolated using a plasmid mini kit from Qiagen. Minipreps were checked for correct integration of the UGCG oligonucleotides by PCR covering the guide oligo insertion site and consecutive sequence analysis.

4.4. Transfection of Lovo Cells with UGCG-gRNA

2.5 × 104 Lovo cells were seeded in a 24-well plate for 24 h and transfected with a mixture of UGCG vector DNA or empty vector as control, P3000 reagent and lipofectamine 3000 (Life Technologies, Darmstadt, Germany) according to the manufacturer’s instructions. The selection of transfected cells with 0.5, 1, and 2 µg puromycin/mL culture medium was started 24 h later. The medium was changed one day later and the cells were cultivated for another 3 days in the presence of puromycin. Cells were expanded thereafter in medium without puromycin. After confluence, cells were split to 6-well plates and then to 10 cm dishes. One aliquot was frozen, and one other analyzed for GSL-depletion as described.

4.5. Sphingolipid Extraction of Colon Carcinoma Cells

Cells were harvested after trypsination, washed with PBS and the pellets extracted with 2 mL CHCl3/CH3OH/H2O 10:10:1 by vol. in an ultrasound water bath at 50 °C for 15 min. Supernatants were collected after centrifugation (10 min, 3000 rpm) and the pellet extracted a second time with 2 mL CHCl3/CH3OH/H2O 30:60:8 by vol. as before. Combined supernatants were evaporated. One half of the extracts was dissolved in 1 mL 0.1 M KOH in methanol and saponified at 50 °C for 4 h. The samples were neutralized with glacial acetic acid and evaporated. The sphingolipids were desalted using reversed phase column chromatography (RP18). Therefore, small glass pipettes were filled with 200 µL of RP18 material (Waters Associates, Milford, MA, USA). The columns were preconditioned each with 2 mL methanol, H2O, and 0.1 M KCl in H2O. The extracts were solved in 1 mL of H2O which was then applied to the columns. The reagent tubes were rinsed twice with 0.1 M KCl, which was then also loaded on the columns. Columns were washed with 2 mL H2O and lipids eluted with 2 mL methanol. The methanol fraction was dried down. GSLs were separated into neutral and acidic components by ion exchange chromatography. Therefore, glass pipettes were filled with 200 µL of DEAE-Sephadex A25 (GE Healthcare, Chicago, IL, USA), and columns were preconditioned with 2 mL of methanol. The samples were solved in 2 mL of methanol and applied to the columns. Reagent tubes were rinsed two times with 1 mL of methanol, and neutral GSLs were completely eluted from the columns with additional 2 mL of methanol. Acidic GSLs were eluted with 2 mL of 0.5 M potassium acetate in methanol. Acidic GSLs were dried and solved in 5 mL of H2O and desalted using preconditioned RP18 columns as described before. An amount corresponding to 0.1 mg of dry intestine was loaded on TLC plates (Merck, Darmstadt, Germany) for the staining of neutral and acidic GSLs. Running solvents are described in the respective Figure Legends. TLC plates were sprayed with 0.2% orcinol in 10% sulfuric acid at 120 °C for 10 min to visualize GSLs.

4.6. Anti-Gb3Cer Immune Overlay

For the detection of Gb3Cer, two GSL-aliquots of Lovo and HCT116 control- and Genz-treated cell extracts, each corresponding to 0.2 mg protein were loaded on a TLC plate (Merck, Darmstadt, Germany). The TLC plate was divided into two parts. One was stained with orcinol reagent as described above to visualize all GSLs. The second plate was fixed with 5% polyisobutylmethacrylate (Sigma, Munich, Germany) in chloroform which was 1:10 diluted in n-hexane. After the organic solvent was evaporated, the plate was blocked with 1% BSA in PBS for 30 min. Blocking solution was removed and the plate subsequently covered with polyclonal chicken anti-Gb3Cer antibody 1:200 diluted in 1% BSA in PBS at 4 °C overnight. The plate was washed five times with PBS/0.05% Tween-20 and incubated with secondary 1:500 diluted alkaline phosphatase linked donkey anti-chicken IgY antibodies (Dianova, Hamburg, Germany) in 1% BSA/PBS for 4 h at RT. After washing for five times, positive bands were detected using Sigma Fast BCIP (Sigma, Munich, Germany).

4.7. Cell Cycle FACS-Analysis with Propidium Iodide (PI)

Cells were cultivated for six days with or without 1 µM/5 µM Genz as described above. Cells were washed with PBS, trypsinized and transferred to 15 mL conical tubes. The tubes were centrifuged at 1500 rpm and supernatant decanted. The residual amount of liquid was carefully removed with a pipette. The cells were suspended in 250 µL PBS by gently pipetting up and down for approximately five times. Ice cold methanol (700 µL, precooled at −20 °C) was added dropwise while slowly vortexing the tubes. The cells were incubated at 4 °C for at least one hour. Approximately 106 cells were added to 4 mL precooled PBS with 1% FCS into FACS tubes and centrifuged at 1500 rpm for 5 min. Cells were stained with 400 µL PI-solution + RNAse A (0.01 mg/mL PI, 0.25 mg RNAse/mL in PBS/1% FCS). Cells were incubated at RT in the dark for 30 min and immediately measured by FACS in linear mode on a FACS Canto with Diva software (BD, East Rutherford, NJ, USA). Analysis of the data was performed using FlowJo V (Tree Star, Flow Cytometry Analysis Software, Ashland, OR, USA).

4.8. Cell Viability Assays

Cells were cultivated in the presence of Genz as described above. The cells were harvested by trypsination, washed with PBS and suspended in PBS/1% FCS, 1 µg/mL PI. The mixture was incubated for 30 min at RT in the dark and subsequently measured by FACS as described.

4.9. Tumor Spheroid Formation of Genz-Treated Cells

Spheroid formation was performed essentially as described [60]. 10,000 cells were placed in each well of a 96-well round bottom ultralow attachment plate (Corning CORN7007, Wiesbaden, Germany) followed by centrifugation at 450× g for 5 min. Spheroids were cultured for 24 h in regular medium which then was carefully exchanged by 0-, 1 µM-, 5 µM- and 10 µM Genz-containing medium for 9 days. Half of the medium was replaced every three days containing the respective Genz concentrations. Spheroid size was determined using a microscope (Nikon, Eclipse TS2) and the surface area calculated with ImageJ after 2, 6, and 9 days.

4.10. Electron Microscopy of Genz-Treated Cells

Lovo and HCT116 cells, cultured on aclar-fluoropolymer-sheets (Science Servoces, Munic, Germay) were treated as described with 1 μM or 10 μM Genz for 6 days. Cells were fixed in 2% formic aldehyde/2% glutaric aldehyde/1 mM CaCl2/1 mM MgCl2/100 mM cacodylate buffer pH 7.2, following post-fixation in 1% OsO4, Uranyl en bloc staining (1% uranyl-acetate in 75% ethanol), dehydration in ethanol and Epon-embedding (Serva, Heidelberg, Germany). Ultrathin sections were cut at 50 nm nominal thickness (UCT, Leica, Wetzlar, Germany), contrasted with uranyl and lead and observed with an EM910 (Carl Zeiss Oberkochen, Germany) equipped with a CCD-Camera (TRS, Morenweis, Germany).

4.11. Western Blotting of Genz-Treated Cells

Control- and Genz-treated cells at ~70% confluency were washed with PBS and lysed by pipetting up- and down in digitonin lysis buffer [20 mM HEPES-NaOH buffer (pH 7.4) containing 25 mM KCl, 250 mM sucrose, 2 mM MgCl2, with freshly added 1% digitonin (Sigma, Munich, Germany), complete protease inhibitors, phospho-stop (Roche, Basel Switzerland) and 0.5 mM DTT]. Cell lysates were incubated on ice for 30 min and subsequently centrifuged at 13,000 rpm at 4 °C for 10 min. Supernatants were collected and protein content determined with Bradford reagent (Sigma, Munich, Germany). 20 µg of protein was used in a 10% SDS gel. The proteins were blotted on a nitrocellulose membrane (Amersham, GE Healthcare, Chicago, IL, USA) and unspecific binding blocked. The membranes were then incubated with primary rabbit Lc3-I/II antibodies (Cell Signaling #12741, Danvers, MA, USA), 1:1000- or with rabbit anti-Tubulin antibodies (Cell Signaling #2128, Danvers, MA, USA), 1:3000 diluted in 5% BSA/TBS at 4 °C overnight. The blots were washed three times with TBS 0.1% tween 20 and incubated with secondary goat anti-rabbit IgG-HRP (Santa Cruz, Heidelberg, Germany), 1:1000 diluted in 5% BSA/TBS at room temperature for 1 h. After three times washing as above, bands were visualized with ECL solution (RPN2109, Amersham/Merck, Darmstadt, Germany) in a ChemiDoc TM Imaging System (Biorad, Feldkirchen, Germany). Quantification was performed with ImageJ.

4.12. Perborate Separation of GlcCer from GalCer

To distinguish GlcCer from GalCer within the remaining double band in the extracts of cells with GCS-inhibition migrating on the height of HexCer, an aliquot corresponding to 0.2 mg protein was loaded together with standard GSLs on a TLC plate (Merck, Darmstadt, Germany). The plate was sprayed with 1.5% sodiumtetraborate solution in H2O, well dried in a vacuum desiccator overnight and then developed in CHCl3/CH3OH/H2O/25% aqueous ammonia, 62.5:30:6:0.5, v/v. The plate was stained with orcinol reagent as described above to visualize the GSLs.

4.13. Animals, Tumor Induction, and Genz-123346-Treatment

C57Bl/6 mice at the age of ~8 weeks received a single dose of 10 mg/kg bodyweight azoxymethane (AOM, Sigma, Munich, Germany) in sterile 0.9% NaCl to initiate CRC [18,61]. The diluted AOM solution was applied i.p. in a volume of 100 µL/10 g bodyweight to each mouse. Furthermore, to promote tumor development, animals received 2% DSS (dextrane sulfate 40, AppliChem, Darmstadt, Germany) in the drinking water for five consecutive days one week after the AOM injection. Mice were fed with a powderized chow diet (# 3437, KLIBA-NAFAG, Kaiseraugst, Switzerland) mashed with an equal amount w/v of sterilized tapped water for five weeks. Thereafter, one group still received soft chow diet and the second cohort received the same soft food supplemented with 0.225% Genz-123346. Mice were kept in a 12 h day/night cycle in a SPF barrier with environmental enrichment. Institutional veterinarians controlled health of the animals. Animal experiments were approved by federal law (Regierungspräsidium Karlsruhe).

4.14. Evaluation of Tumor Incidence

All animals were sacrificed 15 weeks after tumor induction. For evaluation of tumor load and size, the entire colon including the rectum was resected and flushed with ice cold PBS. After longitudinal cut, the colon was spread on a filter paper and immediately immersion fixed with 4% paraformaldehyde in PBS pH 7.4 at 4 °C for 48 h. Tumor numbers in each colon were counted on a stereo microscope. Tumor sizes were determined using a caliper. Formaldehyde fixed colons were divided with a scalpel into three parts (proximal, medial, and distal) and after dehydration with an ascending ethanol gradient subsequently embedded in paraffin for further histological analysis.

4.15. Sphingolipid Extraction of Mouse Organs and Mass Spectrometry

One piece of the intestine, liver, kidney, spleen and heart was lyophilized and powderized. 10 mg of each organ was filled into a separate glass vial and adjusted to extraction. Sphingolipid extraction was performed accordingly as described above for the colon carcinoma cells with the difference that the powderized organs were extracted twice with CHCl3/CH3OH/H2O 10:10:1 by volume.
Isolated sphingolipids including GSLs, Cers, and SMs were investigated by mass spectrometry as described [8,27].

4.16. Immunohistochemistry of Colon

The tissue was cut with a microtome (Microm, Leica, Nussloch, Germany), deparaffinized and immunohistochemistry was performed with rabbit anti-Ki67 antibodies (IHC-00375, Bethyl Laboratories Inc., Montgomery, TX, USA) to stain proliferating cells. Biotin labeled anti-rabbit antibodies (1:200, Dianova, Hamburg, Germany) and AP-streptavidin (1:200, Vector, Burlingame, CA, USA) were used to visualize Ki67-positive cells in colons. Macrophages were stained with rat anti-F4/80 (Acris # 4007, Rockville, MD, USA), 1:500 and secondary biotinylated anti-rat/streptavidin-AP (Vector, Burlingame, CA, USA), 1:200. T cells were stained with rat anti-CD3 (#DIA-303, Hamburg, Germany), 1:50 and secondary biotinylated anti-rat (Vector), 1:200 and streptavidin- AP (Vector, Burlingame, CA, USA), 1:200. Images were taken with a Keyence BZ-9000 microscope (Neu-Isenburg, Germany).

4.17. TUNEL Assay

TUNEL was performed according to the manufacturer’s instructions of the (In Situ Cell Death Detection Kit, Roche, Mannheim, Germany).

4.18. Statistics

Data were analyzed using student’s two-tailed t-test. Graphs show mean values ± SEM. Significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.

5. Conclusions

In conclusion, we have shown that glycosphingolipid (GSL)-depletion by inhibition of glucosylceramide synthase, the major enzyme involved in the initial step of GSL-biosynthesis, led to growth retardation of colon cancer cell-derived tumor microspheres and to an arrest of the cell cycle. In a mouse model mimicking human CRC, marked reduction particularly of colorectal adenomas was achieved by treatment of animals with the GCS-inhibitor Genz-123346. The exact molecular mechanism of the Genz-dependent decrease of the tumor incidence in the CRC-model needs to be further elucidated. However, since inhibitors of GSL-biosynthesis are clinically available, this study may have a direct translational implication as a potential therapeutic application for patients suffering from colorectal cancer.

Supplementary Materials

All data are available online at https://www.mdpi.com/article/10.3390/ijms221910539/s1.

Author Contributions

Conceptualization, R.J., H.-J.G. and R.S.; methodology, R.J., H.-J.G. and R.S.; validation, R.J. and R.S.; investigation, R.J., M.V., F.B., C.S., K.R., S.K. and R.S.; resources, F.B. and J.M.; data curation, R.J. and R.S.; writing—original draft preparation, R.J.; writing—review and editing, R.J., H.-J.G., K.R. and R.S.; supervision, R.J., R.S. and H.-J.G.; funding acquisition, H.-J.G. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by a grant from the German Research Foundation DFG, SFB 1118 to H.-J.G.

Institutional Review Board Statement

Animal experiments were approved by federal law: AZ 35-9185.81/G172/16 (Regierungspräsidium Karlsruhe).

Informed Consent Statement

Not applicable.

Data Availability Statement

All data are available within the main body of the manuscript or in the Supporting information.

Acknowledgments

We thank Karin Müller-Decker for the implementation of the animal experiments with azoxymethane. We thank Almut Schulze for providing the colon carcinoma cells. We are grateful to Peter Nelson for critical proof-reading of the manuscript. The technical support of Gabi Schmidt is gratefully acknowledged.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Rawla, P.; Sunkara, T.; Barsouk, A. Epidemiology of colorectal cancer: Incidence, mortality, survival, and risk factors. Gastroenterol. Rev. 2019, 14, 89–103. [Google Scholar] [CrossRef] [PubMed]
  2. Vogelstein, B.; Fearon, E.R.; Hamilton, S.R.; Kern, S.E.; Preisinger, A.C.; Leppert, M.; Nakamura, Y.; White, R.; Smits, A.M.; Bos, J.L. Genetic Alterations during Colorectal-Tumor Development. N. Engl. J. Med. 1988, 319, 525–532. [Google Scholar] [CrossRef] [Green Version]
  3. Haggar, F.A.; Boushey, R.P. Colorectal Cancer Epidemiology: Incidence, Mortality, Survival, and Risk Factors. Clin. Colon Rectal Surg. 2009, 22, 191–197. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Keum, N.; Giovannucci, E. Global burden of colorectal cancer: Emerging trends, risk factors and prevention strategies. Nat. Rev. Gastroenterol. Hepatol. 2019, 16, 713–732. [Google Scholar] [CrossRef] [PubMed]
  5. Jasperson, K.W.; Tuohy, T.M.; Neklason, D.W.; Burt, R.W. Hereditary and Familial Colon Cancer. Gastroenterology 2010, 138, 2044–2058. [Google Scholar] [CrossRef] [Green Version]
  6. Cunningham, D.; Atkin, W.; Lenz, H.J.; Lynch, H.T.; Minsky, B.; Nordlinger, B.; Starling, N. Colorectal cancer. Lancet 2010, 375, 1030–1047. [Google Scholar] [CrossRef]
  7. Hu, T.; Li, Z.; Gao, C.-Y.; Cho, C.H. Mechanisms of drug resistance in colon cancer and its therapeutic strategies. World J. Gastroenterol. 2016, 22, 6876–6889. [Google Scholar] [CrossRef]
  8. Jennemann, R.; Federico, G.; Mathow, D.; Rabionet, M.; Rampoldi, F.; Popovic, Z.V.; Volz, M.; Hielscher, T.; Sandhoff, R.; Gröne, H.-J. Inhibition of hepatocellular carcinoma growth by blockade of glycosphingolipid synthesis. Oncotarget 2017, 8, 109201–109216. [Google Scholar] [CrossRef] [Green Version]
  9. Marks, D.L.; Dominguez, M.; Wu, K.; Pagano, R.E. Identification of active site residues in glucosylceramide synthase. A nucleotide-binding catalytic motif conserved with processive beta-glycosyltransferases. J. Biol. Chem. 2001, 276, 26492–26498. [Google Scholar] [CrossRef] [Green Version]
  10. D’Angelo, G.; Capasso, S.; Sticco, L.; Russo, D. Glycosphingolipids: Synthesis and functions. FEBS J. 2013, 280, 6338–6353. [Google Scholar] [CrossRef]
  11. Hakomori, S. Bifunctional role of glycosphingolipids. Modulators for transmembrane signaling and mediators for cellular interactions. J. Biol. Chem. 1990, 265, 18713–18716. [Google Scholar] [CrossRef]
  12. Basu, S.; Ma, R.; Mikulla, B.; Bradley, M.; Moulton, C.; Basu, M.; Banerjee, S.; Inokuchi, J.-I. Apoptosis of human carcinoma cells in the presence of inhibitors of glycosphingolipid biosynthesis: I. Treatment of Colo-205 and SKBR3 cells with isomers of PDMP and PPMP. Glycoconj. J. 2004, 20, 157–168. [Google Scholar] [CrossRef]
  13. Deng, W.; Li, R.; Guerrera, M.; Liu, Y.; Ladisch, S. Transfection of glucosylceramide synthase antisense inhibits mouse melanoma formation. Glycobiology 2002, 12, 145–152. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Huang, W.; Tsai, C.; Chen, C.; Chen, T.; Chen, Y.; Lin, Y.; Lu, P.; Lin, C.; Wang, S.; Tsao, C.; et al. Glucosylceramide synthase inhibitor PDMP sensitizes chronic myeloid leukemia T315I mutant to Bcr-Abl inhibitor and cooperatively induces glycogen synthase kinase-3-regulated apoptosis. FASEB J. 2011, 25, 3661–3673. [Google Scholar] [CrossRef] [PubMed]
  15. Lee, Y.-S.; Choi, K.-M.; Lee, S.; Sin, D.-M.; Yoo, K.-S.; Lim, Y.; Lee, Y.-M.; Hong, J.-T.; Yun, Y.-P.; Yoo, H.-S. Myriocin, a serine palmitoyltransferase inhibitor, suppresses tumor growth in a murine melanoma model by inhibiting de novo sphingolipid synthesis. Cancer Biol. Ther. 2012, 13, 92–100. [Google Scholar] [CrossRef] [Green Version]
  16. Weiss, M.; Hettmer, S.; Smith, P.; Ladisch, S. Inhibition of melanoma tumor growth by a novel inhibitor of glucosylceramide synthase. Cancer Res. 2003, 63, 3654–3658. [Google Scholar] [PubMed]
  17. Wingerter, A.; El Malki, K.; Sandhoff, R.; Seidmann, L.; Wagner, D.-C.; Lehmann, N.; Vewinger, N.; Frauenknecht, K.; Sommer, C.; Traub, F.; et al. Exploiting Gangliosides for the Therapy of Ewing’s Sarcoma and H3K27M-Mutant Diffuse Midline Glioma. Cancers 2021, 13, 520. [Google Scholar] [CrossRef]
  18. Neufert, C.; Becker, C.; Neurath, M.F. An inducible mouse model of colon carcinogenesis for the analysis of sporadic and inflammation-driven tumor progression. Nat. Protoc. 2007, 2, 1998–2004. [Google Scholar] [CrossRef]
  19. Liu, Y.-Y.; Patwardhan, G.A.; Xie, P.; Gu, X.; Giuliano, A.E.; Cabot, M.C. Glucosylceramide synthase, a factor in modulating drug resistance, is overexpressed in metastatic breast carcinoma. Int. J. Oncol. 2011, 39, 425–431. [Google Scholar] [CrossRef]
  20. Zhang, C.; Lin, X.; Song, Y.; Zhang, X.; Li, H.; Wang, Q. Overexpression of glucosylceramide synthase and its significance in the clinical outcome of non-small cell lung cancer. Chin. Med. J. 2014, 127, 3071–3076. [Google Scholar]
  21. Zhang, K.; Song, Y.-H.; Lin, X.-Y.; Wang, Q.-X.; Zhang, H.-W.; Xu, J.-W. Upregulation of glucosylceramide synthase protein in papillary thyroid carcinoma. Chin. Med. J. 2013, 126, 4660–4664. [Google Scholar]
  22. Liu, Y.-Y.; Hill, R.A.; Li, Y.-T. Ceramide Glycosylation Catalyzed by Glucosylceramide Synthase and Cancer Drug Resistance. Adv. Cancer Res. 2013, 117, 59–89. [Google Scholar] [CrossRef] [Green Version]
  23. Chester, M.A. IUPAC-IUB joint commission on biochemical nomenclature (JCBN) nomenclature of glycolipids recommendations 1997. J. Mol. Biol. 1999, 286, 963–970. [Google Scholar] [CrossRef]
  24. Hartwig, P.; Höglinger, D. The Glucosylceramide Synthase Inhibitor PDMP Causes Lysosomal Lipid Accumulation and mTOR Inactivation. Int. J. Mol. Sci. 2021, 22, 7065. [Google Scholar] [CrossRef] [PubMed]
  25. Benedix, F.; Kube, R.; Meyer, F.; Schmidt, U.; Gastinger, I.; Lippert, H. Comparison of 17,641 Patients With Right- and Left-Sided Colon Cancer: Differences in Epidemiology, Perioperative Course, Histology, and Survival. Dis. Colon Rectum 2010, 53, 57–64. [Google Scholar] [CrossRef]
  26. Nawa, T.; Kato, J.; Kawamoto, H.; Okada, H.; Yamamoto, H.; Kohno, H.; Endo, H.; Shiratori, Y. Differences between right- and left-sided colon cancer in patient characteristics, cancer morphology and histology. J. Gastroenterol. Hepatol. 2008, 23, 418–423. [Google Scholar] [CrossRef]
  27. Jennemann, R.; Kaden, S.; Sandhoff, R.; Nordstrom, V.; Wang, S.; Volz, M.; Robine, S.; Amen, N.; Rothermel, U.; Wiegandt, H.; et al. Glycosphingolipids are essential for intestinal endocytic function. J. Biol. Chem. 2012, 287, 32598–32616. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Deng, W.; Li, R.; Ladisch, S. Influence of cellular ganglioside depletion on tumor formation. J. Natl. Cancer Inst. 2000, 92, 912–917. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Ranes, M.K.; El-Abbadi, M.; Manfredi, M.G.; Mukherjee, P.; Platt, F.M.; Seyfried, T.N. N-butyldeoxynojirimycin reduces growth and ganglioside content of experimental mouse brain tumours. Br. J. Cancer 2001, 84, 1107–1114. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  30. Inokuchi, J.; Jimbo, M.; Momosaki, K.; Shimeno, H.; Nagamatsu, A.; Radin, N.S. Inhibition of experimental metastasis of murine Lewis lung carcinoma by an inhibitor of glucosylceramide synthase and its possible mechanism of action. Cancer Res. 1990, 50, 6731–6737. [Google Scholar] [PubMed]
  31. Manning, L.S.; Radin, N.S. Effects of the glucolipid synthase inhibitor, P4, on functional and phenotypic parameters of murine myeloma cells. Br. J. Cancer 1999, 81, 952–958. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Obeid, L.; Linardic, C.; Karolak, L.; Hannun, Y. Programmed cell death induced by ceramide. Science 1993, 259, 1769–1771. [Google Scholar] [CrossRef]
  33. Breiden, B.; Sandhoff, K. Emerging mechanisms of drug-induced phospholipidosis. Biol. Chem. 2019, 401, 31–46. [Google Scholar] [CrossRef] [PubMed]
  34. Ellegaard, A.-M.; Bach, P.; Jäättelä, M. Targeting Cancer Lysosomes with Good Old Cationic Amphiphilic Drugs. Rev. Physiol. Biochem. Pharmacol. 2020, 1–46. [Google Scholar] [CrossRef]
  35. Kornhuber, J.; Tripal, P.; Reichel, M.; Mühle, C.; Rhein, C.; Muehlbacher, M.; Groemer, T.; Gulbins, E. Functional Inhibitors of Acid Sphingomyelinase (FIASMAs): A Novel Pharmacological Group of Drugs with Broad Clinical Applications. Cell. Physiol. Biochem. 2010, 26, 9–20. [Google Scholar] [CrossRef]
  36. Ellegaard, A.-M.; Dehlendorff, C.; Vind, A.C.; Anand, A.; Cederkvist, L.; Petersen, N.H.; Nylandsted, J.; Stenvang, J.; Mellemgaard, A.; Østerlind, K.; et al. Repurposing Cationic Amphiphilic Antihistamines for Cancer Treatment. EBioMedicine 2016, 9, 130–139. [Google Scholar] [CrossRef] [Green Version]
  37. Fritz, I.; Wagner, P.; Broberg, P.; Einefors, R.; Olsson, H. Desloratadine and loratadine stand out among common H1-antihistamines for association with improved breast cancer survival. Acta Oncol. 2020, 59, 1103–1109. [Google Scholar] [CrossRef]
  38. Verdoodt, F.; Dehlendorff, C.; Jäättelä, M.; Strauss, R.; Pottegård, A.; Hallas, J.; Friis, S.; Kjaer, S.K. Antihistamines and Ovarian Cancer Survival: Nationwide Cohort Study and in Vitro Cell Viability Assay. J. Natl. Cancer Inst. 2020, 112, 964–967. [Google Scholar] [CrossRef]
  39. Verdoodt, F.; Pottegård, A.; Dehlendorff, C.; Jäättelä, M.; Hallas, J.; Friis, S.; Kjaer, S.K. Antihistamine use and risk of ovarian cancer: A population-based case-control study. Maturitas 2019, 120, 47–52. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Walker, A.; Card, T.; Bates, T.; Muir, K. Tricyclic antidepressants and the incidence of certain cancers: A study using the GPRD. Br. J. Cancer 2010, 104, 193–197. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Xu, W.; Tamim, H.; Shapiro, S.; Stang, M.R.; Collet, J.-P. Use of antidepressants and risk of colorectal cancer: A nested case-control study. Lancet Oncol. 2006, 7, 301–308. [Google Scholar] [CrossRef]
  42. Lucci, A.; Cho, W.I.; Han, T.Y.; Giuliano, A.E.; Morton, D.L.; Cabot, M.C. Glucosylceramide: A marker for multiple-drug resistant cancers. Anticancer Res. 1998, 18, 475–480. [Google Scholar]
  43. Uchida, Y.; Itoh, M.; Taguchi, Y.; Yamaoka, S.; Umehara, H.; Ichikawa, S.-I.; Hirabayashi, Y.; Holleran, W.M.; Okazaki, T. Ceramide Reduction and Transcriptional Up-Regulation of Glucosylceramide Synthase through Doxorubicin-Activated Sp1 in Drug-Resistant HL-60/ADR Cells. Cancer Res. 2004, 64, 6271–6279. [Google Scholar] [CrossRef] [Green Version]
  44. Wegner, M.-S.; Schömel, N.; Gruber, L.; Örtel, S.B.; Kjellberg, M.A.; Mattjus, P.; Kurz, J.; Trautmann, S.; Peng, B.; Wegner, M.; et al. UDP-glucose ceramide glucosyltransferase activates AKT, promoted proliferation, and doxorubicin resistance in breast cancer cells. Cell. Mol. Life Sci. 2018, 75, 3393–3410. [Google Scholar] [CrossRef]
  45. Liu, Y.Y.; Gupta, V.; Patwardhan, G.A.; Bhinge, K.; Zhao, Y.; Bao, J.; Mehendale, H.; Cabot, M.C.; Li, Y.T.; Jazwinski, S.M. Glucosylceramide synthase upregulates MDR1 expression in the regulation of cancer drug resistance through cSrc and beta-catenin signaling. Mol. Cancer 2010, 9, 145. [Google Scholar] [CrossRef] [Green Version]
  46. Sun, Y.; Zhang, T.; Gao, P.; Meng, B.; Gao, Y.; Wang, X.; Zhang, J.; Wang, H.; Wu, X.; Zheng, W.; et al. Targeting glucosylceramide synthase downregulates expression of the multidrug resistance gene MDR1 and sensitizes breast carcinoma cells to anticancer drugs. Breast Cancer Res. Treat. 2010, 121, 591–599. [Google Scholar] [CrossRef]
  47. Wegner, M.-S.; Gruber, L.; Mattjus, P.; Geisslinger, G.; Grösch, S. The UDP-glucose ceramide glycosyltransferase (UGCG) and the link to multidrug resistance protein 1 (MDR1). BMC Cancer 2018, 18, 153. [Google Scholar] [CrossRef]
  48. Roh, J.-L.; Kim, E.H.; Park, J.Y.; Kim, J.W. Inhibition of Glucosylceramide Synthase Sensitizes Head and Neck Cancer to Cisplatin. Mol. Cancer Ther. 2015, 14, 1907–1915. [Google Scholar] [CrossRef] [Green Version]
  49. Tyler, A.; Johansson, A.; Karlsson, T.; Gudey, S.K.; Brännström, T.; Grankvist, K.; Behnam-Motlagh, P. Targeting glucosylceramide synthase induction of cell surface globotriaosylceramide (Gb3) in acquired cisplatin-resistance of lung cancer and malignant pleural mesothelioma cells. Exp. Cell Res. 2015, 336, 23–32. [Google Scholar] [CrossRef] [Green Version]
  50. Wang, T.; Wei, J.; Wang, N.; Ma, J.-L.; Hui, P.-P. The glucosylceramide synthase inhibitor PDMP sensitizes pancreatic cancer cells to MEK/ERK inhibitor AZD-6244. Biochem. Biophys. Res. Commun. 2015, 456, 821–826. [Google Scholar] [CrossRef] [PubMed]
  51. Liu, Y.-Y.; Patwardhan, G.A.; Bhinge, K.; Gupta, V.; Gu, X.; Jazwinski, S.M. Suppression of Glucosylceramide Synthase Restores p53-Dependent Apoptosis in Mutant p53 Cancer Cells. Cancer Res. 2011, 71, 2276–2285. [Google Scholar] [CrossRef] [Green Version]
  52. Patwardhan, G.A.; Zhang, Q.-J.; Yin, D.; Gupta, V.; Bao, J.; Senkal, C.E.; Ogretmen, B.; Cabot, M.C.; Shah, G.V.; Sylvester, P.W.; et al. A New Mixed-Backbone Oligonucleotide against Glucosylceramide Synthase Sensitizes Multidrug-Resistant Tumors to Apoptosis. PLoS ONE 2009, 4, e6938. [Google Scholar] [CrossRef] [Green Version]
  53. Piulats, J.M.; Vidal, A.; García-Rodríguez, F.J.; Muñoz, C.; Nadal, M.; Moutinho, C.; Martínez-Iniesta, M.; Mora, J.; Figueras, A.; Guinó, E.; et al. Orthoxenografts of Testicular Germ Cell Tumors Demonstrate Genomic Changes Associated with Cisplatin Resistance and Identify PDMP as a Resensitizing Agent. Clin. Cancer Res. 2018, 24, 3755–3766. [Google Scholar] [CrossRef] [Green Version]
  54. Salustiano, E.J.; da Costa, K.M.; Freire-De-Lima, L.; Mendonça-Previato, L.; Previato, J.O. Inhibition of glycosphingolipid biosynthesis reverts multidrug resistance by differentially modulating ABC transporters in chronic myeloid leukemias. J. Biol. Chem. 2020, 295, 6457–6471. [Google Scholar] [CrossRef] [PubMed]
  55. Siddiqui, A.; Patwardhan, G.A.; Liu, Y.Y.; Nazzal, S. Mixed backbone antisense glucosylceramide synthase oligonucleotide (MBO-asGCS) loaded solid lipid nanoparticles: In vitro characterization and reversal of multidrug resistance in NCI/ADR-RES cells. Int. J. Pharm. 2010, 400, 251–259. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Stefanovic, M.; Tutusaus, A.; Martinez-Nieto, G.A.; Bárcena, C.; De Gregorio, E.; Moutinho, C.; Barbero-Camps, E.; Villanueva, A.; Colell, A.; Mari, M.; et al. Targeting glucosylceramide synthase upregulation reverts sorafenib resistance in experimental hepatocellular carcinoma. Oncotarget 2016, 7, 8253–8267. [Google Scholar] [CrossRef] [Green Version]
  57. Sohn, O.S.; Fiala, E.S.; Requeijo, S.P.; Weisburger, J.H.; Gonzalez, F.J. Differential effects of CYP2E1 status on the metabolic activation of the colon carcinogens azoxymethane and methylazoxymethanol. Cancer Res. 2001, 61, 8435–8440. [Google Scholar] [PubMed]
  58. Shayman, J.A. Targeting Glucosylceramide Synthesis in the Treatment of Rare and Common Renal Disease. Semin. Nephrol. 2018, 38, 183–192. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Smid, B.E.; Ferraz, M.J.; Verhoek, M.; Mirzaian, M.; Wisse, P.; Overkleeft, H.S.; Hollak, C.E.; Aerts, J.M. Biochemical response to substrate reduction therapy versus enzyme replacement therapy in Gaucher disease type 1 patients. Orphanet J. Rare Dis. 2016, 11, 28. [Google Scholar] [CrossRef] [Green Version]
  60. Kaymak, I.; Maier, C.R.; Schmitz, W.; Campbell, A.D.; Dankworth, B.; Ade, C.P.; Walz, S.; Paauwe, M.; Kalogirou, C.; Marouf, H.; et al. Mevalonate Pathway Provides Ubiquinone to Maintain Pyrimidine Synthesis and Survival in p53-Deficient Cancer Cells Exposed to Metabolic Stress. Cancer Res. 2020, 80, 189–203. [Google Scholar] [CrossRef] [Green Version]
  61. Salcedo, R.; Worschech, A.; Cardone, M.; Jones, Y.; Gyulai, Z.; Dai, R.-M.; Wang, E.; Ma, W.; Haines, D.; O’Huigin, C.; et al. MyD88-mediated signaling prevents development of adenocarcinomas of the colon: Role of interleukin 18. J. Exp. Med. 2010, 207, 1625–1636. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. UGCG expression in human colorectal cancer (CRC) with relation to survival. (A) Sphingolipid synthesis pathway; the enzyme glucosylceramide synthase (GCS) encoded by the gene UGCG is the initial enzyme in the glycosphingolipid (GSL)-biosynthesis pathway. Targeting GCS using genetic approaches or with specific inhibitors such as Genz-123346 disrupts the synthesis of glucosylceramide (GlcCer) and its downstream GSL-products and may lead to accumulation of precursors. (GSLs are abbreviated according to the joint commission on biochemical nomenclature of glycolipids [23]). (B) The expression of UGCG mRNA was lower in human CRC as compared to normal colon. (C) However, patients with high UGCG mRNA expression in colorectal tumors had a reduced overall survival time than patients with lower UGCG expression.
Figure 1. UGCG expression in human colorectal cancer (CRC) with relation to survival. (A) Sphingolipid synthesis pathway; the enzyme glucosylceramide synthase (GCS) encoded by the gene UGCG is the initial enzyme in the glycosphingolipid (GSL)-biosynthesis pathway. Targeting GCS using genetic approaches or with specific inhibitors such as Genz-123346 disrupts the synthesis of glucosylceramide (GlcCer) and its downstream GSL-products and may lead to accumulation of precursors. (GSLs are abbreviated according to the joint commission on biochemical nomenclature of glycolipids [23]). (B) The expression of UGCG mRNA was lower in human CRC as compared to normal colon. (C) However, patients with high UGCG mRNA expression in colorectal tumors had a reduced overall survival time than patients with lower UGCG expression.
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Figure 2. Treatment of Lovo and HCT116 cells with Genz lead to reduced GSL expression and cell cycle arrest. (A) Formula of the GCS inhibitor Genz-123346 (N-[(1R,2R)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-hydroxy-3-pyrrolidin-1-ylpropan-2-yl]nonanamide). (B,C) As shown by thin layer chromatography (TLC), GSL-synthesis was almost completely disrupted by treatment of Lovo (B) and HCT116 cells (C) with 1 µM Genz in the culture medium after 4 and 6 days; x, no GSL-positive band; running solvent for neutral GSLs was CHCl3/CH3OH, H2O, 62.5:30:6 (v/v) and for acidic GSLs CHCl3/CH3OH, 0.2% CaCl2, 60:35:8 (v/v). (D) Anti-Gb3Cer immune overlay of the neutral GSL-fraction from Lovo and HCT116 cells. Chemical staining with orcinol reagent (left) and immune overlay with anti-Gb3Cer antibodies. HCT116 cells expressed globosides in addition to hexosylceramides and lactosylceramides, which were not detectable in Lovo cells. (E,F, quantification) Cell cycle arrest of the Lovo cells in S and G2/M phases occurred after treatment with 1 µM Genz (G,H, quantification). A significant influence on the cell cycle of HCT116 cells as shown by FACS analysis occurred at 5 µM Genz and higher concentrations. (I–L) One micrometer of Genz inhibited growth of tumor spheroids from Lovo (I,J, quantification) and HCT116 cells (K,L, quantification). Note: HCT116 microspheres broke apart with elevated Genz concentrations after longer incubation period (K) and could therefore not be included in the calculations (L, nd, not done); each data point on the graphs represents one biological replicate; scale bars, 100 µM; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
Figure 2. Treatment of Lovo and HCT116 cells with Genz lead to reduced GSL expression and cell cycle arrest. (A) Formula of the GCS inhibitor Genz-123346 (N-[(1R,2R)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)-1-hydroxy-3-pyrrolidin-1-ylpropan-2-yl]nonanamide). (B,C) As shown by thin layer chromatography (TLC), GSL-synthesis was almost completely disrupted by treatment of Lovo (B) and HCT116 cells (C) with 1 µM Genz in the culture medium after 4 and 6 days; x, no GSL-positive band; running solvent for neutral GSLs was CHCl3/CH3OH, H2O, 62.5:30:6 (v/v) and for acidic GSLs CHCl3/CH3OH, 0.2% CaCl2, 60:35:8 (v/v). (D) Anti-Gb3Cer immune overlay of the neutral GSL-fraction from Lovo and HCT116 cells. Chemical staining with orcinol reagent (left) and immune overlay with anti-Gb3Cer antibodies. HCT116 cells expressed globosides in addition to hexosylceramides and lactosylceramides, which were not detectable in Lovo cells. (E,F, quantification) Cell cycle arrest of the Lovo cells in S and G2/M phases occurred after treatment with 1 µM Genz (G,H, quantification). A significant influence on the cell cycle of HCT116 cells as shown by FACS analysis occurred at 5 µM Genz and higher concentrations. (I–L) One micrometer of Genz inhibited growth of tumor spheroids from Lovo (I,J, quantification) and HCT116 cells (K,L, quantification). Note: HCT116 microspheres broke apart with elevated Genz concentrations after longer incubation period (K) and could therefore not be included in the calculations (L, nd, not done); each data point on the graphs represents one biological replicate; scale bars, 100 µM; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
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Figure 3. Miglustat treatment leads to cell cycle arrest in Lovo cells and inhibits growth of Lovo and HCT116 tumor spheroids. (A) Formula of Miglustat. (B,C) n-butyl-deoxynojirimycin (NB-DNJ, Miglustat) inhibits GSL-synthesis of Lovo (B) and HCT116 cells (C) almost completely after four days; x, no GSL-positive band; running solvent for neutral- and acidic GSLs was CHCl3/CH3OH, 0.2% CaCl2, 60:35:8 (v/v). (D,E, quantification) Miglustat treatment led to a visible arrest of the cell cycle in Lovo cells but not in HCT116 cells (F,G, quantification). (H–K) Miglustat inhibited tumor spheroid growth of Lovo- (H,I, quantification) and HCT116 cells (J,K, quantification); each data point on the graphs represents one biological replicate; scale bars, 100 µM; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
Figure 3. Miglustat treatment leads to cell cycle arrest in Lovo cells and inhibits growth of Lovo and HCT116 tumor spheroids. (A) Formula of Miglustat. (B,C) n-butyl-deoxynojirimycin (NB-DNJ, Miglustat) inhibits GSL-synthesis of Lovo (B) and HCT116 cells (C) almost completely after four days; x, no GSL-positive band; running solvent for neutral- and acidic GSLs was CHCl3/CH3OH, 0.2% CaCl2, 60:35:8 (v/v). (D,E, quantification) Miglustat treatment led to a visible arrest of the cell cycle in Lovo cells but not in HCT116 cells (F,G, quantification). (H–K) Miglustat inhibited tumor spheroid growth of Lovo- (H,I, quantification) and HCT116 cells (J,K, quantification); each data point on the graphs represents one biological replicate; scale bars, 100 µM; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
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Figure 4. TLC and cell cycle determination of UGCG-gRNA treated HCT116- and Lovo cells. (A,D) An almost complete depletion of neutral and acidic GSLs was achieved in HCT116- (A) and Lovo cells (D) by UGCG-guide-RNA (gRNA); x, no GSL-positive band; running solvent for neutral- and acidic GSLs was CHCl3/CH3OH, 0.2% CaCl2, 60:35:8 (v/v). (B,C, quantification) UGCG-gRNA treated HCT116 cells did not show an arrest of the cell cycle, similar as HCT116 cells treated with low doses of Genz (Figure 2). (E–G, quantification) Genetic depletion using UGCG-gRNA-application (E) and treatment of Lovo cells with 5 µM Genz (F) resulted in an arrest of the cell cycle, whereas the response in Genz-treated cells was slightly more pronounced; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
Figure 4. TLC and cell cycle determination of UGCG-gRNA treated HCT116- and Lovo cells. (A,D) An almost complete depletion of neutral and acidic GSLs was achieved in HCT116- (A) and Lovo cells (D) by UGCG-guide-RNA (gRNA); x, no GSL-positive band; running solvent for neutral- and acidic GSLs was CHCl3/CH3OH, 0.2% CaCl2, 60:35:8 (v/v). (B,C, quantification) UGCG-gRNA treated HCT116 cells did not show an arrest of the cell cycle, similar as HCT116 cells treated with low doses of Genz (Figure 2). (E–G, quantification) Genetic depletion using UGCG-gRNA-application (E) and treatment of Lovo cells with 5 µM Genz (F) resulted in an arrest of the cell cycle, whereas the response in Genz-treated cells was slightly more pronounced; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
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Figure 5. Lovo and HCT116 cells present an elevated number of multivesicular bodies (MVBs) which contain conspicuous structured vesicles upon Genz treatment. (A) The number of multivesicular bodies with vesicles displaying multilamellar structures was elevated in Genz-treated colon carcinoma cells. MVB-number increased markedly with 1 µM Genz in Lovo cells. Only low numbers of MVBs were seen in HCT116 cells upon treatment with 1 µM Genz. The numbers of MVBs rose markedly with higher Genz concentrations; scale bars, 1 µm. (B) Vesicles inside MVBs of Lovo cells were canonically spheroid, with potential to form onion-like superstructures and myelin-like compaction of stacked membranes (B, insert). (C) MVBs of HCT116 cells displayed angular overall shapes (here triangular), a combination of apparently stiff sheets with sharp cornered rims. The insert demonstrates a widening of the expectedly lipophilic middle-leaflet of the canonical bi-laminar unit-membrane (arrowhead), scale bars in (B,D), 500 nm; in insets 100 nm. (D) The number of MVBs increased with elevated Genz-concentrations; shown are mean numbers of MVBs per µm2 cytosol, each from 10 cells. (E,F) The expression levels of the autophagy marker Lc3-II rose markedly in both Lovo- (E) and HCT116 cells (F) upon increased Genz concentrations; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
Figure 5. Lovo and HCT116 cells present an elevated number of multivesicular bodies (MVBs) which contain conspicuous structured vesicles upon Genz treatment. (A) The number of multivesicular bodies with vesicles displaying multilamellar structures was elevated in Genz-treated colon carcinoma cells. MVB-number increased markedly with 1 µM Genz in Lovo cells. Only low numbers of MVBs were seen in HCT116 cells upon treatment with 1 µM Genz. The numbers of MVBs rose markedly with higher Genz concentrations; scale bars, 1 µm. (B) Vesicles inside MVBs of Lovo cells were canonically spheroid, with potential to form onion-like superstructures and myelin-like compaction of stacked membranes (B, insert). (C) MVBs of HCT116 cells displayed angular overall shapes (here triangular), a combination of apparently stiff sheets with sharp cornered rims. The insert demonstrates a widening of the expectedly lipophilic middle-leaflet of the canonical bi-laminar unit-membrane (arrowhead), scale bars in (B,D), 500 nm; in insets 100 nm. (D) The number of MVBs increased with elevated Genz-concentrations; shown are mean numbers of MVBs per µm2 cytosol, each from 10 cells. (E,F) The expression levels of the autophagy marker Lc3-II rose markedly in both Lovo- (E) and HCT116 cells (F) upon increased Genz concentrations; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
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Figure 6. Genz treatment of Lovo and HCT116 cells lead to a concentration-dependent increase of sphingomyelin (SM). Lipids were quantified by C18-reversed phase UPLC/MS2 in MRM mode using internal standards for each lipid class. Major sphingolipids containing non-hydroxy fatty acids (N) and (C18)-sphingosine (S) were recorded; Cer, ceramide, HexCer: hexosylceramide, SM, sphingomyelin, and PC: phosphatidylcholine. (A,B) HexCer was reduced to a similar extent in Genz- or UGCG-gRNA-treated Lovo (A) or HCT116 cells (B). The SM content in Lovo (A) and HCT116 (B) cells was remarkably elevated upon Genz treatment and much higher as in cells treated with UGCG-gRNA in which the SM-increase correlated vice versa with the reduction of GSLs. The ceramide levels in Lovo and HCT116 cells upon Genz treatment were similar as in controls. (C,D) SM levels in Miglustat-treated Lovo (C) and HCT116 cells (D) were also elevated as compared to controls. Ceramides appeared unaltered upon Miglustat treatment; each data point on the graphs represents one biological replicate; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
Figure 6. Genz treatment of Lovo and HCT116 cells lead to a concentration-dependent increase of sphingomyelin (SM). Lipids were quantified by C18-reversed phase UPLC/MS2 in MRM mode using internal standards for each lipid class. Major sphingolipids containing non-hydroxy fatty acids (N) and (C18)-sphingosine (S) were recorded; Cer, ceramide, HexCer: hexosylceramide, SM, sphingomyelin, and PC: phosphatidylcholine. (A,B) HexCer was reduced to a similar extent in Genz- or UGCG-gRNA-treated Lovo (A) or HCT116 cells (B). The SM content in Lovo (A) and HCT116 (B) cells was remarkably elevated upon Genz treatment and much higher as in cells treated with UGCG-gRNA in which the SM-increase correlated vice versa with the reduction of GSLs. The ceramide levels in Lovo and HCT116 cells upon Genz treatment were similar as in controls. (C,D) SM levels in Miglustat-treated Lovo (C) and HCT116 cells (D) were also elevated as compared to controls. Ceramides appeared unaltered upon Miglustat treatment; each data point on the graphs represents one biological replicate; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
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Figure 7. Genz treatment lowered the incidence of experimental CRC in vivo. (A) Scheme of the treatment course. CRC was induced in C57Bl6 mice with azoxymethane (AOM) at the age of 8 weeks, followed by a tumor promoting 5-day cycle of dextrane sulfate (DSS) applied by the drinking water starting one week after the AOM-treatment. Mice, n = 24, received chow diet until five weeks after tumor induction. Then one cohort of animals, n = 10, received 0.225% Genz in the food. All animals were sacrificed 15 weeks after tumor induction according to the termination criteria from the animal application. (B) Scheme of the human and murine intestinal tract. Colorectal tumors in humans develop preferentially in the areas of the sigmoid colon and the rectum but also in other areas of the large intestine. In this mouse model, we observed tumors predominantly restricted to the rectal area of the colon with a critical load at fifteen weeks after tumor induction. (C) Treatment of mice with Genz resulted in a markedly lower number of colorectal tumors in the distal part of the colon. (D) The size of tumors detected in the colons of Genz-treated mice was also notably smaller as compared to chow fed mice; each data point represents the mean size of all tumors detected in one mouse; significances are *, p ≤ 0.05; **, p < 0.01.
Figure 7. Genz treatment lowered the incidence of experimental CRC in vivo. (A) Scheme of the treatment course. CRC was induced in C57Bl6 mice with azoxymethane (AOM) at the age of 8 weeks, followed by a tumor promoting 5-day cycle of dextrane sulfate (DSS) applied by the drinking water starting one week after the AOM-treatment. Mice, n = 24, received chow diet until five weeks after tumor induction. Then one cohort of animals, n = 10, received 0.225% Genz in the food. All animals were sacrificed 15 weeks after tumor induction according to the termination criteria from the animal application. (B) Scheme of the human and murine intestinal tract. Colorectal tumors in humans develop preferentially in the areas of the sigmoid colon and the rectum but also in other areas of the large intestine. In this mouse model, we observed tumors predominantly restricted to the rectal area of the colon with a critical load at fifteen weeks after tumor induction. (C) Treatment of mice with Genz resulted in a markedly lower number of colorectal tumors in the distal part of the colon. (D) The size of tumors detected in the colons of Genz-treated mice was also notably smaller as compared to chow fed mice; each data point represents the mean size of all tumors detected in one mouse; significances are *, p ≤ 0.05; **, p < 0.01.
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Figure 8. The number of colorectal adenomas were reduced in Genz-treated mice. (A) Ki67 staining indicated proliferative cells in colons of mice. Both Genz-treated mice and controls developed predominantly adenomas with its typical polypoid-like shape (A,B, middle images) and only low numbers of adenocarcinomas (A,B, lower images). However, Genz-feeding markedly reduced the number of adenomas as compared to chow-fed controls (B). (C) The number of Ki67 positive cells in the colorectal parts of the colons was lower in crypts of Genz-treated mice as compared to controls; each data point represents mean numbers of Ki67 positive cells of approximately 50 crypts per mouse. Counted were positive cells only from completely vertically cut villi apart from the tumor areas; significances are *, p ≤ 0.05; ***, p < 0.001. (D, F4/80) Both Genz-fed mice and controls lacked macrophage infiltrations in the tumor but showed an enrichment in peritumoral areas. (D, CD3) Only a few cells stained positive with the T cell marker CD3; T, tumor area. Genz treatment did not lead to increased apoptosis (D, TUNEL); a few cells with smaller nuclei than epithelial cells stained positive in tumors of treated mice and controls; scale bars, 100 µM.
Figure 8. The number of colorectal adenomas were reduced in Genz-treated mice. (A) Ki67 staining indicated proliferative cells in colons of mice. Both Genz-treated mice and controls developed predominantly adenomas with its typical polypoid-like shape (A,B, middle images) and only low numbers of adenocarcinomas (A,B, lower images). However, Genz-feeding markedly reduced the number of adenomas as compared to chow-fed controls (B). (C) The number of Ki67 positive cells in the colorectal parts of the colons was lower in crypts of Genz-treated mice as compared to controls; each data point represents mean numbers of Ki67 positive cells of approximately 50 crypts per mouse. Counted were positive cells only from completely vertically cut villi apart from the tumor areas; significances are *, p ≤ 0.05; ***, p < 0.001. (D, F4/80) Both Genz-fed mice and controls lacked macrophage infiltrations in the tumor but showed an enrichment in peritumoral areas. (D, CD3) Only a few cells stained positive with the T cell marker CD3; T, tumor area. Genz treatment did not lead to increased apoptosis (D, TUNEL); a few cells with smaller nuclei than epithelial cells stained positive in tumors of treated mice and controls; scale bars, 100 µM.
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Figure 9. Genz treatment alters the sphingolipid composition in the intestine. (A) TLC-analysis of neutral and acidic GSLs from the intestine of Genz-treated mice. The intestine of adult mice contained predominantly the neutral GSLs HexCer and GA1. Lipids were quantified by C18-reversed phase UPLC/MS2 in MRM mode using internal standards for each lipid class except for GA1, which was normalized to internal HexCer standards. Sphingolipids containing either non-hydroxy fatty acids (N) or alpha-hydroxy fatty acids (A) in combination with (C18)-sphingosine (S) or with (C18)-phytosphingosine (P) were recorded; Cer: ceramide, HexCer, hexosylceramide, GA1: asialo-ganglioside 1 or gangliotetraosylceramide (Gg4Cer, see Figure 1A), and SM: sphingomyelin. (B,C) MS2-analysis of HexCer (B) and GA1 (C). AS- as well as NS-species markedly decreased in the intestine of Genz-treated mice. AP-GSLs were less effectively downregulated. Genz-application did not lead to a reduction of NP-GSLs; for designation of ceramide anchors, see abbreviations. (D) NP-Cers increased in intestines of Genz-treated mice as compared to chow-fed controls. (E) The SM content was markedly elevated and PC remained essentially unaltered upon Genz treatment; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
Figure 9. Genz treatment alters the sphingolipid composition in the intestine. (A) TLC-analysis of neutral and acidic GSLs from the intestine of Genz-treated mice. The intestine of adult mice contained predominantly the neutral GSLs HexCer and GA1. Lipids were quantified by C18-reversed phase UPLC/MS2 in MRM mode using internal standards for each lipid class except for GA1, which was normalized to internal HexCer standards. Sphingolipids containing either non-hydroxy fatty acids (N) or alpha-hydroxy fatty acids (A) in combination with (C18)-sphingosine (S) or with (C18)-phytosphingosine (P) were recorded; Cer: ceramide, HexCer, hexosylceramide, GA1: asialo-ganglioside 1 or gangliotetraosylceramide (Gg4Cer, see Figure 1A), and SM: sphingomyelin. (B,C) MS2-analysis of HexCer (B) and GA1 (C). AS- as well as NS-species markedly decreased in the intestine of Genz-treated mice. AP-GSLs were less effectively downregulated. Genz-application did not lead to a reduction of NP-GSLs; for designation of ceramide anchors, see abbreviations. (D) NP-Cers increased in intestines of Genz-treated mice as compared to chow-fed controls. (E) The SM content was markedly elevated and PC remained essentially unaltered upon Genz treatment; significances are *, p ≤ 0.05; **, p < 0.01; ***, p < 0.001.
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Jennemann, R.; Volz, M.; Bestvater, F.; Schmidt, C.; Richter, K.; Kaden, S.; Müthing, J.; Gröne, H.-J.; Sandhoff, R. Blockade of Glycosphingolipid Synthesis Inhibits Cell Cycle and Spheroid Growth of Colon Cancer Cells In Vitro and Experimental Colon Cancer Incidence In Vivo. Int. J. Mol. Sci. 2021, 22, 10539. https://doi.org/10.3390/ijms221910539

AMA Style

Jennemann R, Volz M, Bestvater F, Schmidt C, Richter K, Kaden S, Müthing J, Gröne H-J, Sandhoff R. Blockade of Glycosphingolipid Synthesis Inhibits Cell Cycle and Spheroid Growth of Colon Cancer Cells In Vitro and Experimental Colon Cancer Incidence In Vivo. International Journal of Molecular Sciences. 2021; 22(19):10539. https://doi.org/10.3390/ijms221910539

Chicago/Turabian Style

Jennemann, Richard, Martina Volz, Felix Bestvater, Claudia Schmidt, Karsten Richter, Sylvia Kaden, Johannes Müthing, Hermann-Josef Gröne, and Roger Sandhoff. 2021. "Blockade of Glycosphingolipid Synthesis Inhibits Cell Cycle and Spheroid Growth of Colon Cancer Cells In Vitro and Experimental Colon Cancer Incidence In Vivo" International Journal of Molecular Sciences 22, no. 19: 10539. https://doi.org/10.3390/ijms221910539

APA Style

Jennemann, R., Volz, M., Bestvater, F., Schmidt, C., Richter, K., Kaden, S., Müthing, J., Gröne, H. -J., & Sandhoff, R. (2021). Blockade of Glycosphingolipid Synthesis Inhibits Cell Cycle and Spheroid Growth of Colon Cancer Cells In Vitro and Experimental Colon Cancer Incidence In Vivo. International Journal of Molecular Sciences, 22(19), 10539. https://doi.org/10.3390/ijms221910539

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