1. Introduction
The most commonly diagnosed cancer in the world is lung cancer. In 2020, it was estimated that of 19.3 million new cancer cases worldwide, approximately 2.2 million or 11.4% will be lung cancer. In terms of mortality, lung cancer was estimated at 1.8 million deaths representing 18% of all cancer deaths [
1]. Lung cancer can be classified into two major subtypes, small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), with the vast majority (approximately 85%) falling into the latter subtype. Traditionally treatment of lung cancer has been associated with poor outcomes; however, recent advances in immunotherapy [
2], targeted therapy [
3] and the discovery of new actionable mutations [
4] have greatly increased the treatment options available, in particular for NSCLC.
Aberrant regulatory mechanisms are common in NSCLC and it is now well established that epigenetics is one such regulatory mechanism with significant alterations in NSCLC [
5]. Epigenetics can be loosely defined as a series of modifications on either the DNA or histones which together can collectively be called the “epigenetic code” or “epigenome” [
6,
7]. This code is generated and utilized by a large number of proteins which can be classified as either “readers”, “writers” or “erasers” depending on their function to regulate gene expression [
8]. Of these, a large number of proteins contain a plant homeodomain (PHD) that recognizes either methylated or acetylated residues on histones [
8,
9,
10] and are considered “…central “readers” of histone post-translational modifications” [
9]. Numbering more than 100 proteins [
9], these include a small subset of proteins called the JADE family [
11]. Originally identified and described as “Gene for Apoptosis and Differentiated Epithelia” [
12], this family comprises three members designated as PHF17 (JADE1), PHF16 (JADE2) and PHF15 (JADE3) [
11].
Epigenetics has now been classified as a new “Hallmark of Cancer” with a designation for “nonmutational epigenetic reprogramming” as an enabling characteristic that facilitates the acquisition of original hallmark capabilities, and also enables the provisional new hallmark capability of phenotypic plasticity [
13], and as such defining such the functional roles of these epigenetic readers in cancer is of importance. Our knowledge regarding the actual functional roles of the JADE family is limited. The initial characterization of JADE1 found that it formed an interaction with the von Hippel–Lindau (pVHL) protein and the lysine acetyltransferase Tip60 (KAT5) to direct acetylation at histone H4 [
14]. Further studies determined that JADE1 is also part of the HBO1 complex, a large complex containing multiple histone/lysine acetyltransferases (including Tip60), and was found to be critical with respect to this complex directing acetylation specifically at histone H4 to regulate transcription [
15,
16]. Subsequent studies have found that the N-terminal region of JADE1 acts as the platform necessary to bring the catalytic HBO1 subunit to its cognate H3–H4 substrate in this regard to elicit acetylation [
17]. The HBO1 complex itself plays important roles in various molecular processes including transcription, DNA replication, and DNA repair [
18], and JADE1 has been shown to play essential roles in regulating chromatin during mitosis [
19,
20]. JADE2 has been shown to form a complex with the lysine methylase LSD1 during neurogenesis and cognitive function [
21,
22], and has also been linked to myogenesis [
23]. The HBO1 complex has a distinctive characteristic in that it has the presence of three PHD finger domains in two different subunits: tumor suppressor proteins ING4/5 and JADE1/2/3. The PHD domains in JADE1 were shown to be essential for (a) HBO1 complexes to bind chromatin and (b) for a critical JADE1-associated tumor suppressor activity [
24], and it is important to note that the HBO1 complex has been shown to play important roles in cancer [
18].
Despite the large body of evidence linking the HBO1 complex with cancer, overall, there have been very few studies examining the actual role of JADE family proteins themselves in cancer. Critical roles for JADE1 have been identified in renal cell carcinoma [
25,
26,
27,
28,
29]. In ovarian cancer, JADE2 has been shown to be highly overexpressed and may function to regulate YAP1 a critical ovarian cancer oncogene [
30], whilst a gene fusion between JADE2 and NUP98 has been observed in a pediatric acute myeloid leukemia [
31]. In colon cancer, JADE3 has been shown to promote increased tumourigenicity by increasing cancer stem cell properties [
32].
However, an examination of JADE family members in NSCLC has not been studied to any great degree. Most recently, a link between a single nucleotide polymorphism (SNP—rs329118) in JADE2 and the risk of developing NSCLC has been identified [
33]. As such, in this manuscript, we set out to assess the expression of JADE2 in NSCLC to determine if its expression also had any potential utility as a biomarker in lung cancer at both the mRNA and protein levels. We show that JADE2 is predominantly downregulated in NSCLC at the mRNA but not at protein level, and that expression of JADE2 has prognostic value and is associated with a better 5-year overall survival (OS). Links between JADE2 expression and other genes commonly associated with NSCLC are described, along with the identification of novel mutated genes that affect JADE2 expression. Correlations between JADE2 expression and various parameters such as tumor mutational burden and immune cell infiltration are explored. The results presented suggest that JADE2 may be a candidate biomarker in NSCLC and warrants further study.
2. Materials and Methods
2.1. Nomenclature
Nomenclature for genes and proteins used the current HUGO definitions [
34].
2.2. Cell Culture
Twelve cell lines (comprising normal human bronchial epithelial cell lines (HBECs) and NSCLC cancer cell lines) were used in this study comprising: normal bronchial epithelial cells (HBEC3, HBEC4 and HBEC5 Beas2B) and NSCLC cell lines with various histotypes as follows: adenocarcinoma (A549, NCI-H2228, NCI-H1975, HCC827 and H3122), squamous cell carcinoma (SKMES-1), large cell carcinoma (NCI-H460) and adenosquamous (NCI-H596).
HBECs 3–5 [
35], HCC827, NCI-H1975 and NCI-H3255 were a gift from Prof. John D Minna (Hamon Centre for Therapeutic Oncology Research, UT Southwestern, Dallas, TX, USA). The A549, SKMES-1, NCI-H460, NCI-H1299 and NCI-H596 cell lines were purchased from the ATCC (LGC Promochem, Teddington, UK). NCI-H3122 cells were a kind gift from Dr. Dong-Wan Kim, Seoul National University Hospital, Seoul, Republic of Korea).
All cells were maintained in a humidified atmosphere containing 5% CO
2 in appropriate media supplemented with 10% fetal bovine serum (FBS), and Antibiotic Antimycotic Solution (Sigma-Aldrich, St. Louis, MO, USA: Cat No: A5955) with the exception of HBECs. HBECs were grown in Keratinocyte Growth Medium 2 (Promocell, Heidelberg, Germany; Cat. No: C-20111), and on collagen-coated plates. A549 cells were grown in Nutrient Mixture F-12 Ham (Sigma-Aldrich, St. Louis, MO, USA—Cat. No: N6658), SKMES-1 in Dulbecco′s Modified Eagle′s Medium—high glucose (Sigma-Aldrich, St. Louis, MO, USA—Cat. No: D6429). All other NSCLC cell lines were grown in RPMI-1640 Medium (Sigma-Aldrich, St. Louis, MO, USA—Cat. No: R8758). All cell lines were routinely tested for mycoplasma as per the published PCR protocol [
36].
2.3. Primary Tumor Samples
Chemotherapy naïve tumor specimens surgically resected were used in this study. All samples were evaluated by a pathologist immediately following resection and tumor tissue along with matched normal tissue were removed and flash-frozen for downstream analysis. Comprising 11 adenocarcinomas and 11 squamous cell carcinomas a summary of their clinical and histopathological data is summarized in
Table 1. Prior to surgery informed consent for bio-banking was obtained from each patient, and for retrospective analyses individual consent was waived. The study proceeded only after formal approval from the SJH/AMNCH Hospital Ethics Committee—Ethics REC (No.: 041018/8804; Project ID: 0624), and in accordance with the Declaration of Helsinki (as revised in 2013).
2.4. Formalin Fixed Paraffin Embedded Samples
A total of 204 surgically resected NSCLC tumor specimens from the period 1999–2007 were included in this study (Ethics REC (No.: 041018/8804; Project ID: 0624)). All surgically resected tumor specimens and control specimens were fixed with 10% formalin and embedded in paraffin (FFPE). Samples were staged using The Union for International Cancer Control Tumor-Node-Metastasis (TNM) Classification of Malignant Tumors 8th edition [
37,
38] and subsequently subtyped histologically using World Health Organization guidelines [
39].
Table 2 presents a summary of the available clinical and histopathological data (including age, sex, smoking status, histology, TNM stage, surgical procedure, tumor grade, and primary site) for the patients used in this TMA previously described by us [
40,
41].
A Beecher Manual Tissue Arrayer (Estigen OÜ, Tartu, Estonia-Model MTA-1) was used to generate a tissue microarray (TMA) containing quadruplicate cores (0.6 mm) of the FFPE embedded samples and a 4 µm section of this TMA was subsequently used for immunohistochemistry (IHC) of JADE2.
2.5. Immunohistochemistry
IHC was performed on TMA sections by utilizing a standard protocol to deparaffinize, rehydrate and wash the slides. Subsequently, ULTRA cell conditioning (ULTRA CC1), pH9.1, was used for heat-induced epitope retrieval (HIER). For JADE2 antibody staining, slides were incubated with rabbit polyclonal primary antibody HPA055789 (Atlas Antibodies Bromma, Sweden, Merck—Atlas Antibodies Cat#HPA055789, RRID: AB_2682922) diluted in Roche antibody diluent (Roche Diagnostics 05261899001) (1:10) for 64 min at ambient temperature and stained using the OptiViewTM DAB IHC detection kit (Roche Diagnostics 06396500001) on a Roche/Ventana BenchMark XT processor.
Following IHC, staining was independently assessed by two pathologists blinded to the clinical, pathological and follow-up data. Staining intensity was designated as either 0, 1+, 2+ or 3+, and each tumor section was given an H score between 0–300 = 3(% at 3+) + 2(% at 2+) +1(% at 1+). No samples were observed with an overall H Score of 300.
Tumors with high JADE2 expression were designated as those with an average H score above the median value and low expression below the median. Kaplan–Meier analyses were constructed using Prism 5.01 (GraphPad, San Diego, CA, USA).
2.6. RNA Isolation, RT-PCR and qPCR Amplification
Total RNA was isolated and converted to complementary DNA (cDNA) using our previously described methodology [
42,
43,
44]. In brief, total RNA was extracted using TRI reagent (Molecular Research Center, Montgomery Road, OH, USA) according to the manufacturer’s instructions. A sample of 250 ng of this total RNA was then pre-treated to remove contaminating genomic DNA with amplification grade DNase I (Sigma-Aldrich, St. Louis, MO, USA—AMPD1-1KT) according to the manufacturer’s instructions [
42,
43,
44]. ReadyScript
®® cDNA Synthesis Mix (Sigma-Aldrich, St. Louis, MO, USA—Cat RDRT) was then used to generate the first strand cDNA according to the manufacturer’s instructions [
42,
43,
44].
Real-Time qPCRs for JADE2 (absolute quantification method) were subsequently conducted on these samples using an Applied Biosystems™ StepOnePlus™ Real-Time PCR System PCR platform (Thermo Fisher Scientific, Waltham, MA, USA—Cat 4376598) and 2x SYBR Green qPCR Master Mix (Bimake, Houston, TX, USA—Cat B21403) using the manufacturer’s protocol in a 2-step qPCR program with a synthesized GBlock for JADE2 as the standard using the following primers:
JADE2 FWD: 5′-ATCTGCGGCAGGACCTAGAG-3′
JADE2 REV: 5′-GAGTTTGCAGATGGCGTGTT-3′
The following cycling parameters were used:
An initial polymerase activation of 95 °C for 2 min followed by 35 cycles of 95 °C 15 s and annealing/amplification at 58 °C for 45 s. A melt curve analysis was conducted at the end of the PCR. The data were analyzed using either the default in-built StepOne software (Version 2.3), exported and graphed using Prism 5.01.
Endpoint RT-PCR to examine all members of the JADE family was conducted using the following primers
JADE1 FWD: 5′-GCAGCCTCTGCAATGAGAAG-3′
JADE1 REV: 5′-GCAGCCTCTGCAATGAGAAG-3′
JADE2 (same primers as above)
JADE3 FWD: 5′-GAGTTTGCAGATGGCGTGTT-3′
JADE3 REV: 5′-GAGTTTGCAGATGGCGTGTT-3′
For Endpoint RT-PCR the following primers were used to amplify 18S rRNA [
45] for use as a housekeeping gene/loading control.
18S rRNA Forward 5′-GATGGGCGGCGGAAAATAG-3′
18S rRNA Reverse 5′-GGCGTGGATTCTGCATAATGG-3′
The same amplification protocol was used for RT-PCR as above. All PCR products were gel electrophoresed on either 2% (18S rRNA) or 4% agarose (JADE1-3), and the PCR products were visualized using an LI-COR ODYSSEY FC imaging system (LI-COR, Lincoln, NE, USA).
2.7. JADE2 Overexpression Studies
A JADE2 overexpression plasmid was generated by PCR of the full-length JADE2 cDNA with primers incorporating appropriate restriction enzyme sites:
JADE2 3.1(-) EcoRV FWD:
5′-TGCTGGATATCATGGAAGAGAAGAGGCGAAAATACT-3′
JADE2 3.1(-) HindIII REV:
5′-CTTAAGCTTTTAGGAGGCCAGTACGCCCATGCGG-3′.
The PCR products were digested with EcoRV/Hind III, and purified and cloned into similarly digested pCDNA3.1(-) (Thermo Fisher Scientific, Waltham, MA, USA—Cat. No: V795-20).
KAN/NEO FWD:
5′-GGCTATGACTGGGCACAACAG-3′
KAN/NEO REV:
5′-CGCTTCAGTGACAACGTCGA-3′
All PCR products were gel electrophoresed on 2% agarose, and the PCR products were visualized using an LI-COR ODYSSEY FC imaging system (LI-COR, Lincoln, NE, USA).
Overexpression studies using this construct were conducted by transfecting NCI-H1975 with either pCDNA3.1(-) Empty Vector Control or with pCDNA3.1(-)—JADE2 using Fugene HD according to the manufacturer’s instructions (Promega, Madison, WI, USA Cat. No: E2311). A mixed pool of stable integrants was obtained by selection with G418 at 1000 µg/mL, and subsequently used for cellular proliferation assays.
2.8. Validations of Expression Differences for JADE2 in NSCLC
Validation of altered JADE2 mRNA expression in the TCGA NSCLC cohorts was conducted through Lung Cancer Explorer (LCE) [
46] using the comparative analysis setting.
Altered JADE2 protein expression in the TCGA-LUAD and LUSC datasets was interrogated using cProSite [
47] to interrogate the datasets of the National Cancer Institute’s Clinical Proteomic Tumor Analysis Consortium (CPTAC). These datasets comprise LUAD—comprising 110 tumors, with 101 tumors paired with normal adjacent tissue samples—and LUSC—comprising 108 tumors with 99 paired normal adjacent tissue—which have global proteome data available for interrogation [
48,
49].
2.9. Survival Analysis for JADE2
To examine whether JADE2 mRNA expression has any prognostic value with respect to patient survival, KM-Plot was utilized [
50] using a univariate analysis incorporating a Cox proportional hazards model with median expression as the cut-off.
2.10. Associations with Key NSCLC Genes, Oncogenic Driver Mutations and Novel Mutated Genes
Associations between JADE2 and the expression of key genes commonly overexpressed or mutated in NSCLC were examined using TIMER2.0 [
51] using the modules Gene_Corr, and Gene_Mutation. The muTarget platform was used to interrogate the TCGA datasets containing RNA-sequencing and mutation data to identify novel mutated genes that result in significant changes in the expression of JADE2 in NSCLC compared to the corresponding wild-type gene expression. The analysis was conducted using JADE2 as the target gene and with mutation prevalence set at 2% [
52].
2.11. Correlations between JADE2 Expression, Tumor Mutational Burden and Immune Infiltrations in NSCLC
Correlations between tumor mutational burden (TMB) and JADE2 mRNA expression were examined using cBioPortal [
53]. To interrogate how altered expression of JADE2 expression was associated with tumor-infiltrating immune cells (TIICs) in NCSLC we used TIMER [
54] and TIMER2.0 [
51]. TIMER and TIMER2.0 calculate gene expression levels against tumor purity, and results are presented based on a purity-corrected partial Spearman’s rho value with associated statistical significance.
2.12. Correlations between JADE2 Expression and Anti-Cancer Drug Sensitivity in NSCLC Cell Lines
The DepMap PRISM repurposing Primary Screen was used to conduct an online analysis restricted to NSCLC cell lines for drugs potentially capable of targeting JADE2 [
55].
2.13. Drug Treatment and Cellular Viability Assays
Ornidazole was purchased from Selleck (St. Louis, MO, USA; cat. no. O7753), and dissolved in ethanol at a final concentration of 200 mM. Next, 2000 cells were plated per well in a 96-well plate and serum-starved (0.5%
v/
v FBS) for 24 h prior to the addition of either drug or vehicle and incubated for a further 24 h. Cellular viability was assessed using a resazurin reduction assay as previously described [
45].
2.14. Statistical Analysis
All data are expressed as mean ± SEM unless stated otherwise. Statistical analysis was performed with GraphPad Prism 5.01 (GraphPad, La Jolla, CA, USA). Correlations between JADE2 expression and any given parameter were evaluated using the nonparametric Mann–Whitney U-test (for two categories) or Spearman’s correlation as indicated. Kaplan–Meier curves were performed for survival curves, and statistical analysis was assessed using the log-rank (Mantel–Cox) test. Total overall survival (OS) was defined as the time from the date of surgery to death. The 5-year OS was defined as the time from the date of surgery up to a cut-off of five years post-surgery. Patients who were still alive or lost to follow-up were treated as censored data in the survival analysis. Overall, 95% confidence intervals (CIs) were used throughout the analysis. Statistical significance was defined as p < 0.05.
Availability of data and materials:
The data that support the findings presented in this study are available for interrogation at the following online resources:
4. Discussion
The role of PHD-domain-containing proteins as potential therapeutic targets in cancer is well established [
61]. Many proteins contain PHD domains [
9], and one small family of proteins called the JADE family has been shown to play various roles in cancer. During the preparation of this manuscript, a link between a particular SNP (rs329118 T>C) in JADE2 and the risk of developing NSCLC was established [
33]. In this manuscript, we examined the expression of JADE2 in NSCLC. Initial analysis of all three JADE mRNAs identified JADE2 as the main JADE family member expressed in NSCLC cell lines (
Figure 1).
Yang et al. suggested that JADE2 mRNA was elevated in NSCLC, but our data (
Figure 2A) and subsequent analysis of the TCGA datasets (
Figure 2B,C) show that overall JADE2 mRNA is either not affected or significantly downregulated in NSCLC tumors. Further analysis showed that JADE2 protein was not significantly altered between adjacent normal lung tissue and LUAD tumors (
Figure 2D) or LUSC (
Figure 2E). This suggests that JADE2 is not generally overexpressed at either the mRNA or protein level in NSCLC. To assess if JADE2 mRNA had any prognostic value an in silico bioinformatic analysis on JADE2 mRNA expression in NSCLC was conducted using KM-Plotter [
50]. From this analysis, it was shown that high expression of JADE2 mRNA was associated with a better OS in all NSCLC (
Figure 4A—84 months vs. 52 months). When stratified by histology this OS benefit was restricted to LUAD (
Figure 4B), but not LUSC (
Figure 4C). When re-analyzed for progression-free survival (PFS) the same results were observed (
Supplementary Figure S8).
While the JADE2 protein does not appear to be significantly altered in NSCLC, its mRNA expression was shown to have potential value to predict both patient OS (
Figure 4) and PFS (
Supplementary Figure S7). As such we optimized conditions to conduct IHC and developed a staining intensity scoring (H score) (
Figure 3) to allow for an analysis of NSCLC patient TMA for OS. From this initial analysis, it was shown that overall there was no OS benefit (
Figure 4D). Traditionally, however, for patients with NSCLC median OS and 5-year survival rates have historically been poor [
1]. When re-analyzed for 5-year OS, a significant OS benefit was however observed in patients with high expression of JADE2 (
Figure 4E). The disparity between these observations may reflect the age group of the cases examined (
Table 2), as the majority of patients were over 65 at the time of surgery and some patients in the full survival dataset may have died as a consequence of other factors (for example old age or other co-morbidities). The data, therefore, suggest that JADE2 protein expression may have potential clinical use for predicting or stratifying patients who will have better 5-year survival.
To determine if JADE2 expression could be associated with other genes known to be important in NSCLC tumorigenesis, in the first instance we assessed if there were any correlations between their overall expression and that of JADE2 mRNA. Positive correlations between JADE2 mRNA expression and some of the examined genes were observed in EGFR and PIK3CA (
Table 3) for both LUAD and LUSC. In only one instance was a positive correlation found between ERBB2 mRNA in LUAD, whereas a corresponding correlation was not observed in LUSC (
Table 3). This suggests that perhaps JADE2 may play a role in regulating the transcription of these important NSCLC genes but further analysis will be required. As another member of the JADE family JADE1 has been linked to renal cancer pathogenesis through a VHL-mutation-dependent mechanism [
62], we next sought to determine if JADE2 mRNA was also associated with mutation of key oncogenic driver mutations in NSCLC such as KRAS or ALK [
4]. The results clearly found no associations between the majority of oncogenic drivers, with the exception of CDKN2A which was found to have an association with JADE2 mRNA expression in LUSC (
Table 4). This suggests that JADE2 mRNA does not play any significant role in the regulation or stabilization of oncogenic driver mutated mRNA/protein in NSCLC. Using muTarget we subsequently assessed if any genes mutated in NSCLC are affected by JADE2 mRNA expression and identified several such (
Figure 5). Several of these such as HECW1 (
Figure 5G) or ZNF800 (
Figure 5I) have been previously shown to have roles in NSCLC pathogenesis [
63,
64] or in pre-cancerous settings such as COPD (KRT34,
Figure 5E). Whether or not mutated forms of these genes play functional roles in NSCLC tumorigenesis has yet to be elucidated, but preliminary analysis by us suggests that high expression of HECW2 and ZNF800 mRNA is associated with a better OS, whilst high expression of HECW1 and KRT34 is associated with poor OS, and an assessment of these markers for prognostic value linked to mutational status may be warranted.
TMB is a hotly researched area in NSCLC as a high TMB has been linked to better patient responses to ICI [
56,
57]. To interrogate whether or not JADE2 mRNA is linked to TMB, we first used a surrogate approach first described by Feng and Shen [
57], to examine if there were any correlations between JADE2 mRNA and genes associated with both the DDR or MMR repair pathways (
Table 5). The results suggest that JADE2 mRNA is positively associated with these pathways and may therefore be associated with TMB. In agreement with this, when analyzed a positive correlation between JADE2 mRNA and PD-L1 mRNA (a key ICI target in NSCLC) was observed for both LUAD (
Figure 6A) and LUSC (
Figure 6B), suggesting that indeed JADE2 mRNA could correlate with TMB. One of the significant issues in the use of TMB for stratifying patients into those that can receive ICI concerns the methodology to detect TMB (defined as “…the number of somatic mutations per megabase of interrogated genomic sequence” [
65]) is the cost per assay [
66], and so a simplified assay such as JADE2 mRNA levels that could help predict patient’s sensitivity to ICI would be of potential benefit. However, we then assessed JADE2 mRNA levels with actual TMB in NSCLC, there was an actual negative correlation between JADE2 mRNA and TMB in LUAD (
Figure 6C; Spearman’s correlation −0.34;
p = 1.9 × 10
−7), and no correlation between TMB and JADE2 mRNA in LUSC (
Figure 6D).
Another potential indicator for response to ICI in NSCLC is TIICs and, in particular, CD8+ T cell infiltration [
67]. Analysis of the TCGA datasets for TIICs that correlate with JADE2 mRNA expression identified that at least in LUAD JADE2 mRNA was strongly associated with CD8+ T cell infiltration in NSCLC (
Table 6a). Significant associations for many other TIICs were also observed for LUAD, in particular, CD4+ T cells, neutrophils and dendritic cells (
Table 6a), while few associations were observed for LUSC with the exception of CD4+ T cells and dendritic cells (
Table 6a). When associated with patient survival, only B cell and dendritic cell infiltration were found to have any survival benefit in LUAD (
Table 6b). Immune cell exhaustion is also associated with resistance or lack of response to ICI [
67,
68]. We subsequently assessed whether JADE2 mRNA was associated with well-established markers of T Cell exhaustion and observed positive correlations between JADE2 mRNA and markers of immune cell exhaustion (
Table 7), and a second analysis using a different methodological approach subsequently confirmed that a six-gene signature for markers of T cell exhaustion is positively correlated with JADE2 mRNA (
Figure 7). Overall, the results described above indicate that JADE2 mRNA may not be suitable as a candidate biomarker to predict overall response to ICI in NSCLC; however, future studies will be required to delineate its roles in CD8+ T cell infiltration and regulation of PD-L1 expression and to assess it as a potential biomarker to predict T cell exhaustion in NSCLC.
Ornidazole an antiprotozoal antibiotic was identified through analysis of the Cancer Dependency Map [
55] as a potential drug that could be repurposed for use in NSCLC. In this regard, ornidazole was previously studied as a modifier of hypoxia in various cancer clinical trials [
69,
70], with no significant improvement observed for lung cancer [
70]. However, the peak plasma concentration of ornidazole observed in the astrocyte study was 40 mg/l [
70], which equates to approximately 180 µM. Interestingly the DepMap data which suggested that JADE2 mRNA was associated with sensitivity to ornidazole used an 8-step, 4-fold dilution of ornidazole, starting from 10 µM. Our results for sensitivity to ornidazole demonstrated that at least in concentrations similar to those used in earlier trials that there was some sensitivity to ornidazole at the 150–200 µM range (and beyond). However, this sensitivity was also observable in normal bronchial epithelial cells, suggesting that as a stand-alone repurposing agent, ornidazole should not be considered suitable for further evaluation in NSCLC. To further test if JADE2 expression had any role in sensitivity to ornidazole a cell line stably overexpressing JADE2 was generated (
Figure 8D,E), and when sensitivity to this drug was assessed overexpression of JADE2 did not affect sensitivity (
Figure 8F). It must be noted that the methodology used to measure the effects on cellular proliferation by us and that used by DepMap for their chemical-perturbation viability screens is very different, and may require additional refinements/re-assessments to determine if ornidazole could be repurposed (maybe in combination with standard chemotherapy) in NSCLC. Moreover, a recent study in melanoma suggests that ornidazole could play a role in suppressing CD133+ stem cells [
71], and CD133+ is commonly expressed in NSCLC [
72,
73], and be a potential novel target [
74,
75].