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16 pages, 681 KB  
Article
SOX9, GATA3, and GATA4 Overexpression in Liposarcomas: Insights into the Molecular Biology of Adipocytic Sarcomas
by Andrei-Ionuț Patrichi, Zsolt Kovács, Ioan Jung and Simona Gurzu
Int. J. Mol. Sci. 2025, 26(22), 10981; https://doi.org/10.3390/ijms262210981 - 13 Nov 2025
Abstract
Liposarcomas represent a heterogeneous group of malignant mesenchymal neoplasms, with diverse histological subtypes and molecular alterations. This study aimed to investigate the gene expression profiles of SOX9, GATA3, and GATA4 in liposarcoma subtypes and to assess their associations with clinicopathological parameters. Forty-two formalin-fixed, [...] Read more.
Liposarcomas represent a heterogeneous group of malignant mesenchymal neoplasms, with diverse histological subtypes and molecular alterations. This study aimed to investigate the gene expression profiles of SOX9, GATA3, and GATA4 in liposarcoma subtypes and to assess their associations with clinicopathological parameters. Forty-two formalin-fixed, paraffin-embedded liposarcoma samples were analyzed. Total RNA was extracted, reverse-transcribed, and quantified by qRT-PCR using GAPDH as an endogenous control. Relative quantification (RQ) values were categorized, and statistical analyses included Fisher’s exact test, Kaplan–Meier survival analysis, and Cox proportional hazards modeling. SOX9 expression significantly varied among histological subtypes (p = 0.017), with ALT/WDLS cases showing a predominance of high-level expression (RQ > 50 in 12/15 cases), in contrast to myxoid subtypes clustering mainly in the 10–50 RQ range. GATA4 overexpression correlated with smaller tumor size (<100 mm) (p = 0.049), being more frequent in 15/20 small tumors compared to 10/22 larger ones. GATA3 and GATA4 demonstrated the strongest inter-gene correlation (r = 0.68, p < 0.05), suggesting possible functional interplay. Kaplan–Meier analysis revealed no statistically significant survival differences for individual gene expression, but a high combined GATA3–GATA4 signature was associated with a favorable trend. These findings indicate that SOX9, GATA3, and GATA4 are broadly upregulated in liposarcomas, with subtype- and size-dependent expression patterns. The strong association between GATA3 and GATA4 expression supports their potential synergistic role in tumor biology. Integration of these molecular markers into diagnostic and prognostic workflows may enhance subtype characterization and inform targeted therapeutic strategies. Further studies in larger cohorts are warranted to validate these biomarkers and explore their mechanistic interplay in liposarcoma pathogenesis. Full article
(This article belongs to the Special Issue Current Research on Cancer Biology and Therapeutics: Fourth Edition)
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17 pages, 6618 KB  
Article
Transcriptome Analysis of Natural Albino Northern Snakehead (Channa argus var.) Provides Novel Insights into Color-Related Genes
by Yunbang Zhang, Qunxiang Ruan, Yiping Liu, Xin Wei, Ling Wang, Yunfei Chen, Jian Gao, Yuanchao Zou and Xiaojuan Cao
Fishes 2025, 10(11), 582; https://doi.org/10.3390/fishes10110582 (registering DOI) - 13 Nov 2025
Abstract
The northern snakehead (Channa argus) is an important economic fish species that holds a significant position in Chinese aquaculture due to its high nutritional value, fast growth, and anti-hypoxia capacity. There is a natural albino-mutant (AM) C. argus strain. Albinism, a [...] Read more.
The northern snakehead (Channa argus) is an important economic fish species that holds a significant position in Chinese aquaculture due to its high nutritional value, fast growth, and anti-hypoxia capacity. There is a natural albino-mutant (AM) C. argus strain. Albinism, a stable genetic trait characterized by loss of body pigmentation, provides a unique opportunity to study the molecular mechanisms of vertebrate coloration. This study investigates the molecular mechanisms underlying albinism in C. argus through skin transcriptomic analyses of wild type (WT) and AM individuals. Morphological and histological analysis revealed no significant phenotypic difference between WT and AM in early development, whereas adult AM exhibited a severe reduction in melanocytes. Through RNA sequencing of skin tissues from WT-adult, AM-adult, and AM-15dpf, a total of 10,891 differentially expressed genes (DEGs) were identified. Through DEG enrichment analyses, we identified a series of enriched pathways and genes related to albinism, including melanogenesis (i.e., tyr, tyrp1b, kitb, kitlga, pmela, pmelb, mitfa, and mitfb) and xanthophore formation (i.e., pax3a, pax3b, pax7a, and sox10). In conclusion, this study not only enriches the research on fish pigmentation, but also has potential significance for the aquaculture and breeding of C. argus. Full article
(This article belongs to the Section Genetics and Biotechnology)
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27 pages, 2148 KB  
Article
Less Severe Inflammation in Cyclic GMP–AMP Synthase (cGAS)-Deficient Mice with Rabies, Impact of Mitochondrial Injury, and Gut–Brain Axis
by Pannatat Areekul, Thansita Bhunyakarnjanarat, Sakolwan Suebnuson, Kollawat Somsri, Somchanok Trakultritrung, Kris Taveethavornsawat, Tewin Tencomnao, Siwaporn Boonyasuppayakorn and Asada Leelahavanichkul
Biology 2025, 14(11), 1583; https://doi.org/10.3390/biology14111583 - 12 Nov 2025
Abstract
Activation of cGAS, a receptor recognizing cytosolic DNA, in macrophages might be associated with rabies (an RNA virus) through mitochondrial damage. A similar mortality rate was observed between cGAS-deficient (cGAS-/-) and wild-type (WT) mice post-CVS-11 strain injection. However, 2 out of 12 cGAS-/- [...] Read more.
Activation of cGAS, a receptor recognizing cytosolic DNA, in macrophages might be associated with rabies (an RNA virus) through mitochondrial damage. A similar mortality rate was observed between cGAS-deficient (cGAS-/-) and wild-type (WT) mice post-CVS-11 strain injection. However, 2 out of 12 cGAS-/- mice (but not WT) survived for 15 days post-injection. At 7 days post-infection, less severe brain inflammation in cGAS-/- mice was demonstrated by the viral abundance in the hippocampus, the expression of proinflammatory genes (TNF-α and IL-1β), and the Evans blue dye assay (blood–brain barrier defect) with the presence of higher anti-inflammatory genes (TGF-β and arginase-1). Fecal Proteobacteria was more prominent in the infected WT mice, while serum cytokines (TNF-α and IL-1β) were similar in both mouse strains. There were less prominent responses against the rabies virus in cGAS-/- macrophages than in WT cells, as indicated by supernatant IL-6 and the gene expression of TLR-3, RIG-1, MDA-5, and iNOS. On the other hand, mitochondrial injury and cGAS activation were more prominent in WT macrophages over cGAS-/- cells, as indicated by cGAS expression, supernatant cGAMP (a secondary messenger of cGAS), and mitochondrial oxidative stress (MitoSox) together with a decrease in mitochondrial DNA and maximal respiration (extracellular flux analysis). In conclusion, (i) rabies-damaged mitochondria led to cGAS activation that was less severe in cGAS-/- than in WT, (ii) rabies-induced dysbiosis was demonstrated, and (iii) cGAS manipulation and gut–brain axis-associated inflammation warrants further investigation. Full article
(This article belongs to the Special Issue The Role of Gut Microbiota in Human Metabolism and Disease)
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19 pages, 8168 KB  
Article
Data-Driven Optimization of Ship Propulsion Efficiency and Emissions Considering Relative Wind
by Sang-A Park, Min-A Je, Suk-Ho Jung and Deuk-Jin Park
J. Mar. Sci. Eng. 2025, 13(11), 2120; https://doi.org/10.3390/jmse13112120 - 9 Nov 2025
Viewed by 175
Abstract
The relative wind is a significant but underexplored influencing factor on the tradeoff between propulsion efficiency and pollutant emissions for ships. In this study, full-scale measurements obtained from four voyages of the training ship of Baekkyung were used to quantify the effects of [...] Read more.
The relative wind is a significant but underexplored influencing factor on the tradeoff between propulsion efficiency and pollutant emissions for ships. In this study, full-scale measurements obtained from four voyages of the training ship of Baekkyung were used to quantify the effects of relative wind on ship propulsion efficiency and pollutant emissions. The collected navigational, engine performance, and emission data—including parameters such as shaft power, engine load, specific fuel oil consumption (SFOC), and NOx and SOx concentrations—were synchronized and then analyzed using statistical methods and a generalized additive model (GAM). Statistical correlation analysis and a GAM were applied to capture nonlinear relationships between variables. Compared with linear models, the GAM achieved higher predictive accuracy (R2 = 0.98) and effectively identified threshold and interaction effects. The results showed that headwind conditions increased the engine load by ~12% and SFOC by 8.4 g/kWh while tailwind conditions reduced SFOC by up to 6.7 g/kWh. NOx emissions peaked under headwind conditions and exhibited nonlinear escalation beyond a relative wind speed of 12 kn. An operational window was identified for simultaneous improvement of the propulsion efficiency and reduction in pollutant emissions under beam wind and tailwind conditions at moderate relative wind speeds of 6–10 kn and an engine load of 30–40%. These findings can serve as a guide for incorporating relative wind into operational strategies for maritime autonomous surface ships. Full article
(This article belongs to the Special Issue Advanced Research on Path Planning for Intelligent Ships)
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19 pages, 5839 KB  
Article
Analysis of OTX2, PAX6, and SOX2 Gene and Protein Expression Patterns in Ocular Development of Human and Rat Embryos
by Anna Junga, Mara Pilmane and Pavlo Fedirko
Int. J. Mol. Sci. 2025, 26(22), 10845; https://doi.org/10.3390/ijms262210845 - 8 Nov 2025
Viewed by 157
Abstract
Transcription factors orthodenticle homeobox 2 gene (OTX2), paired box 6 gene (PAX6), and SRY-box transcription factor 2 gene (SOX2) are key regulators of ocular morphogenesis; however, their comparative embryonic localization across species—and the correspondence between transcript and [...] Read more.
Transcription factors orthodenticle homeobox 2 gene (OTX2), paired box 6 gene (PAX6), and SRY-box transcription factor 2 gene (SOX2) are key regulators of ocular morphogenesis; however, their comparative embryonic localization across species—and the correspondence between transcript and protein distributions—remain incompletely defined. Chromogenic in situ hybridization (CISH) was employed to detect OTX2, PAX6, and SOX2 transcripts, while biotin–streptavidin immunohistochemistry (IHC) was used to assess Otx2, Pax6, and Sox2 protein expression. A semi-quantitative scoring system was applied to evaluate positive structures across ocular compartments. Transcripts were predominantly localized to the retina in both species, with occasional low-level expression in the optic nerve, sclera, and eyelid. Proteins displayed broader distributions: Otx2 was abundant in the retina and eyelid, while Pax6 and Sox2 were detected in multiple tissues, including cornea and extraocular muscles. OTX2, PAX6, and SOX2 show retina-predominant transcription and wider protein expression across ocular tissues. These findings highlight spatial differences between transcript and protein localization, supporting a complex regulatory framework underlying vertebrate eye development. Full article
(This article belongs to the Section Molecular Biology)
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27 pages, 1234 KB  
Article
Evaluating the Environmental Footprint of Steel-Based Bottle Closures: A Life Cycle Assessment Approach
by Irini Spyrolari, Alexandra Alexandropoulou, Eleni Didaskalou and Dimitrios Georgakellos
J. Exp. Theor. Anal. 2025, 3(4), 35; https://doi.org/10.3390/jeta3040035 - 7 Nov 2025
Viewed by 149
Abstract
This research presents a detailed Life Cycle Assessment (LCA) of 26 mm Crown cork metal closures used in glass bottle packaging, with the objective of quantifying and comparing their environmental impacts across all life cycle stages. This study adheres to ISO 14040 and [...] Read more.
This research presents a detailed Life Cycle Assessment (LCA) of 26 mm Crown cork metal closures used in glass bottle packaging, with the objective of quantifying and comparing their environmental impacts across all life cycle stages. This study adheres to ISO 14040 and ISO 14044 standards and utilizes Microsoft Excel for structuring and documenting input–output data across each phase. The LCA encompasses three primary stages: raw material production (covering iron ore extraction and steel manufacturing), manufacturing processes (including metal sheet printing, forming, and packaging of closures), and the transport phase (distribution to bottling facilities). During the Life Cycle Inventory (LCI), steel production emerged as the most environmentally burdensome phase. It accounted for the highest emissions of carbon dioxide (CO2), carbon monoxide (CO), nitrogen oxides (NOx), and sulphur oxides (SOx), while emissions of heavy metals and volatile organic compounds were found to be negligible. The Life Cycle Impact Assessment (LCIA) was carried out using the Eco-Indicator 99 methodology, which organizes emissions into impact categories related to human health, ecosystem quality, and resource depletion. Final weighting revealed that steel production is the dominant contributor to overall environmental impact, followed by the manufacturing stage. In contrast, transportation exhibited the lowest relative impact. The interpretation phase confirmed these findings and emphasized steel production as the critical stage for environmental optimization. This study highlights the potential for substantial environmental improvements through the adoption of low-emission steel production technologies, particularly Electric Arc Furnace (EAF) processes that incorporate high percentages of recycled steel. Implementing such technologies could reduce CO2 emissions by up to 68%, positioning steel production as a strategic focus for sustainability initiatives within the packaging sector. Full article
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24 pages, 3188 KB  
Article
Integrated Assessment of Benthic Bacterial Community Physiology, Structure, and Function Across C, N, P, and S Gradients in Lake Villarrica Sediments, Chile
by Tay Ruiz-Gil, Sebastián Elgueta, Giovanni Larama, Joaquín-Ignacio Rilling, Anthony Hollenback, Deb P. Jaisi, Diego Valdebenito, Bryan M. Spears and Marco A. Campos
Microorganisms 2025, 13(11), 2544; https://doi.org/10.3390/microorganisms13112544 - 7 Nov 2025
Viewed by 281
Abstract
Benthic bacterial communities play a critical role in nutrient cycling and are highly sensitive to environmental pollution. This study aimed to investigate the physiological, compositional and functional responses of bacterial communities across a range of carbon (C), nitrogen (N), phosphorus (P), and sulfur [...] Read more.
Benthic bacterial communities play a critical role in nutrient cycling and are highly sensitive to environmental pollution. This study aimed to investigate the physiological, compositional and functional responses of bacterial communities across a range of carbon (C), nitrogen (N), phosphorus (P), and sulfur (S) gradients in sediments from Lake Villarrica, Chile. Sediment samples were collected from 5 sites representing a gradient of nutrient pressure from the lake basin (NL < PuB < PoP < SL < VB). Nutrient forms (TC, TN, TP, TS, and OM) were chemically quantified. Community function was assessed via community-level physiological profiles (CLPPs) using Biolog® EcoPlates (C substrates), PM3B (N substrates), and PM4A (P and S substrates). Function and composition were assessed based on total bacterial and functional nutrient-cycling gene abundances (16Sr RNA, chiA, mcrA, nifH, amoA, nosZ, phoD, pqqC, soxB, dsrA) using qPCR and 16S rRNA metabarcoding, respectively. In general, the CLPPs were higher for C substrates, followed by P, S, and N substrates, with metabolism of organic forms of these nutrients preferential, and P-cycling genes were the most abundant in the lake. Spatially, the most nutrient-enriched site (VB) showed a significantly (p ≤ 0.05) higher nutrient content (e.g., 5.4% TC, 0.54% TN, 1302.8 mg kg−1 TP and 854.1 mg kg−1 TS) and total bacterial abundance (2.9 × 1011 gene copy g−1 dw sediment) but displayed lower CLPPs (from 0.63 to 1.02 AWCD) and nutrient-cycling gene abundances (e.g., 9.1 × 101, 2.7 × 103, 3.6 × 103 and 4.7 × 103 gene copy g−1 dw sediment for chiaA, nifH, phoD and dsrA, respectively) compared to the less nutrient-enriched sites (e.g., NL). The bacterial community composition shifted accordingly, with Bacillota enriched in VB and Planctomycetota occurring more frequently in less nutrient-exposed sites. Functional prediction analysis revealed enhanced methanotrophy and sulfate respiration in nutrient-rich sediments, whereas nitrification and organic P (Po) mineralization dominated in less impacted areas. The results demonstrate that nutrient enrichment constrains bacterial functional diversity in Lake Villarrica and, so, may be useful indicators of environmental stress to be considered in pollution monitoring programmes. Full article
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23 pages, 914 KB  
Article
Genetic Analysis of Patients with Chronic Thromboembolic Pulmonary Hypertension (CTEPH): A Single-Center Observational Study
by Zsuzsanna Bereczky, Gábor Kolodzey, Sarolta Borsos, László Balogh, Petra Erzsébet Biró, Éva Molnár, Katalin Rázsó, Andrea Péter, Judit Barta and Tibor Szűk
Genes 2025, 16(11), 1336; https://doi.org/10.3390/genes16111336 - 6 Nov 2025
Viewed by 287
Abstract
Background/Objectives: Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare disease, in which multiple genetic and environmental factors may contribute. This study aimed to identify potential genetic determinants in patients with CTEPH and to compare their occurrence to a control group, which included [...] Read more.
Background/Objectives: Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare disease, in which multiple genetic and environmental factors may contribute. This study aimed to identify potential genetic determinants in patients with CTEPH and to compare their occurrence to a control group, which included patients with pulmonary embolism who had not developed CTEPH. Methods: Tier 1 and 2 genes related to coagulation, fibrinolysis and platelet disorders—as recommended by the International Society on Thrombosis and Haemostasis—and genes associated with vascular conditions were analyzed in n = 15 patients with CTEPH and n = 17 controls using next-generation sequencing. Non-synonymous, rare variants were collected and interpreted. Results: As expected, no single gene or variant was consistently present among CTEPH patients. Instead, individuals carried different mutations and combinations of variants. We identified several variants that were not found in the control group. Candidate variants were detected in F12, F13A1, F13B, F5, KNG1, SERPIND1, THBD, ADAMTS13, VWF, STIM1, ETV6, THPO, MPL, SERPINA1, ENG, RASA1, ACVRL1, GDF2, NFE2, SOX17 and RNF213. We did not detect exclusive variants in FGA, CPB2, and BMPR2 although they were suggested as candidates in previous studies. Elevated factor VIII and von Willebrand factor in CTEPH could not be explained by mutations in VWF and F8. Conclusions: Our study supports the hypothesis of heterogeneous genetic background in CTEPH, involving multiple pathways such as coagulation, altered fibrinolysis and impaired angiogenesis. These results provide a basis for more detailed investigations into specific genes and variants potentially associated with CTEPH in larger cohorts. Full article
(This article belongs to the Section Human Genomics and Genetic Diseases)
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32 pages, 10076 KB  
Article
Characterising PMP22-Proximal Partners in a Schwann Cell Model of Charcot–Marie–Tooth Disease Type1A
by Ian Holt, Nicholas Emery, Monte A. Gates, Sharon J. Brown, Sally L. Shirran and Heidi R. Fuller
Biology 2025, 14(11), 1552; https://doi.org/10.3390/biology14111552 - 5 Nov 2025
Viewed by 366
Abstract
Charcot–Marie–Tooth disease type 1A (CMT1A) is a hereditary condition caused by the duplication of the PMP22 gene. Overexpression of peripheral myelin protein 22 in Schwann cells leads to myelin sheath defects and axonal loss. We have produced a cell model to facilitate studies [...] Read more.
Charcot–Marie–Tooth disease type 1A (CMT1A) is a hereditary condition caused by the duplication of the PMP22 gene. Overexpression of peripheral myelin protein 22 in Schwann cells leads to myelin sheath defects and axonal loss. We have produced a cell model to facilitate studies of the molecular mechanisms involved in PMP22 accumulation and clearance. Our model is a stably transfected, clonal, immortalised human Schwann cell line with overexpressed levels of PMP22 fusion protein. A control-transfected cell line (vector lacking PMP22) was also produced. PMP22-transfected cells had reduced levels of mitosis, with the PMP22 fusion protein concentrated in punctate aggregates in the cytoplasm and expressed at the plasma membranes, which were often irregular and spindly. In contrast, control cells (control-transfected and parent cell lines) generally had smooth and regular plasma membrane morphology. Culturing in the presence of NRG1 and forskolin lead to upregulation of markers of myelination potential in the control cells. These markers were more variable in the cells stably transfected with PMP22, including decreased levels of transcripts of SOX10, JUN, S100B and NGFR, but increased levels of MPZ and EGR2 compared to controls. Using proximity-dependent biotin identification (BioID2), several hundred proteins were identified in the proximity of the overexpressed PMP22, of which 291 significant proteins were only detected in the proximity of PMP22 and not in that of control pull-downs. Among the most significantly enriched PMP22-interacting proteins were integrins alpha-2 (ITGA2) and alpha-7 (ITGA7), which play a role in myelination via their interactions with the extracellular matrix. The presence of ITGA2 in just the PMP22-transfected fraction was confirmed by western blot. Some of the proteins were associated with several enriched molecular pathways, including molecular transport and protein trafficking, and may represent potential therapeutic targets for CMT1A by promoting the degradation and enhanced trafficking of PMP22. Full article
(This article belongs to the Section Neuroscience)
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21 pages, 4106 KB  
Article
Therapeutic Effect of Alpha Linolenic Acid on Cutaneous Wound Healing in Hyperglycemic Mice: Involvement of Neurotrophins
by Thais Paulino do Prado, Flávia Cristina Zanchetta, Aline Cristina Rosa Maria, Thaiane da Silva Rios, Guilherme Rossi de Assis-Mendonça, Maria Helena Melo Lima, Dennys Esper Correa Cintra, Joseane Morari, Lício A. Velloso and Eliana P. Araújo
Pharmaceutics 2025, 17(11), 1427; https://doi.org/10.3390/pharmaceutics17111427 - 4 Nov 2025
Viewed by 379
Abstract
Background: Alpha-linolenic acid (ALA) is an essential fatty acid from the omega-3 family that plays an important role in skin homeostasis. It is known for its anti-inflammatory properties, which can contribute to wound healing. Neurotrophins, such as Brain-Derived Neurotrophic Factor (BDNF), may also [...] Read more.
Background: Alpha-linolenic acid (ALA) is an essential fatty acid from the omega-3 family that plays an important role in skin homeostasis. It is known for its anti-inflammatory properties, which can contribute to wound healing. Neurotrophins, such as Brain-Derived Neurotrophic Factor (BDNF), may also play an important role in the skin, influencing nerve regeneration and pain modulation. Objectives: This article aims to explore the therapeutic effect of ALA on wound healing in streptozotocin-induced hyperglycemic mice, with an emphasis on the involvement of neurotrophins. Methods: We used keratinocyte cultures exposed or not to ALA and male C57BL6-J mice, which were randomly divided into four groups: non-hyperglycemic treated with vehicle; non-hyperglycemic treated with ALA; hyperglycemic treated with vehicle; and hyperglycemic treated with ALA. The treatment was administered continuously via a subcutaneous osmotic pump. Results: We found that controlled ALA administration potentiates the wound healing process in hyperglycemic mice by accelerating the inflammatory phase and promoting early granulation tissue formation (73.2% ± 0.7 vs. 92.2% ± 2.8 on day 7, n = 5; p < 0.05). This is supported by the balance between the expression of vimentin, CD31, and MMP-9. Furthermore, ALA modulates proteins linked to peripheral neurogenesis and gliogenesis, such as BDNF, NTRK2, SOX-10, CNTF, CTNFR, and STAT-3. It may also promote wound healing and nerve regeneration at the wound site in hyperglycemic animals. In non-hyperglycemic mice, ALA improves the quality of scars but does not accelerate the wound healing process, even with the positive modulation of certain genes relevant to skin healing. Conclusions: Alpha-linolenic acid improves skin wound healing and increases gene expression related to nerve regeneration in wounds of hyperglycemic mice. Full article
(This article belongs to the Section Gene and Cell Therapy)
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12 pages, 2027 KB  
Article
Anticancer and Immunomodulatory Effects of a Thiazolyl Benzodiazepine Targeting HSP90 in ER+ Breast Cancer
by Kubra Acikalin Coskun, Lutfi Tutar, Kezban Uçar Çifci, Mervenur Al, Irfan Koca, Mehmet Gumus, Levent Gulum, Emir Capkinoglu and Yusuf Tutar
Pharmaceuticals 2025, 18(11), 1665; https://doi.org/10.3390/ph18111665 - 4 Nov 2025
Viewed by 267
Abstract
Background: Heat shock protein 90 (HSP90) is a molecular chaperone that stabilizes numerous oncogenic proteins and supports tumor survival. Small molecules targeting HSP90 offer a novel approach to overcome drug resistance and immune suppression in breast cancer. Methods: A novel thiazolyl benzodiazepine (TB) [...] Read more.
Background: Heat shock protein 90 (HSP90) is a molecular chaperone that stabilizes numerous oncogenic proteins and supports tumor survival. Small molecules targeting HSP90 offer a novel approach to overcome drug resistance and immune suppression in breast cancer. Methods: A novel thiazolyl benzodiazepine (TB) containing a hydrazone moiety was evaluated in breast cancer cell lines (ER+ MCF-7, TNBC MDA-MB-231, and HER2+ SK-BR-3). Cytotoxicity was assessed using the CCK-8 assay, followed by PCR sequencing, flow cytometry, RT-qPCR, protein profiling, and HSP90 binding assays. Results: TB showed the strongest activity in MCF-7 cells (IC50 = 7.21 µM) compared to MDA-MB-231 (IC50 = 28.07 µM) and SK-BR-3 (IC50 = 12.8 µM) cells. Mechanistic studies showed that TB binds to HSP90 (Kd = 3.10 µM), leading to disruption of the oncogenic signal. TB induced G2/M cell cycle arrest, promoted apoptosis via Bax and Caspase-3 activation, and suppressed cancer stem cell markers (NANOG, OCT4, SOX2). Additionally, TB activated immune-related pathways via ERK/MAPK signaling and upregulated genes such as SMAD2, SMAD3, and JUN.Conclusions: TB functions as an HSP90 inhibitor with dual anticancer and immunomodulatory properties in Estrogen Receptor-Positive (ER+) breast cancer cells. These findings suggest that TB represents a promising scaffold for the development of multi-targeted breast cancer therapies. Full article
(This article belongs to the Section Medicinal Chemistry)
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23 pages, 1432 KB  
Review
Can Molecular Attributes of Mammalian Granulosa Cells and Ovarian Putative Stem Cells Predestine Them to Be a Promising Tool for Tissue Engineering and Regenerative Medicine?
by Małgorzata Duda and Marcin Samiec
Int. J. Mol. Sci. 2025, 26(21), 10667; https://doi.org/10.3390/ijms262110667 - 1 Nov 2025
Viewed by 271
Abstract
Granulosa cells (GCs) and ovarian putative stem cells (oPSCs) represent distinct but complementary populations within the mammalian ovary. While GCs have long been considered terminally differentiated and hormonally specialized, emerging evidence indicates that they retain epigenetic plasticity and, under defined conditions, can be [...] Read more.
Granulosa cells (GCs) and ovarian putative stem cells (oPSCs) represent distinct but complementary populations within the mammalian ovary. While GCs have long been considered terminally differentiated and hormonally specialized, emerging evidence indicates that they retain epigenetic plasticity and, under defined conditions, can be reprogrammed into cells exhibiting pluripotent-like features. In contrast, oPSCs, including oogonial stem cells (OSCs) and very small embryonic-like stem cells (VSELs), are naturally multipotent and capable of spontaneous or inducible differentiation into neural, endothelial, and other somatic lineages. Both cell types express stemness-related markers, such as OCT4, SOX2, and c-KIT, and demonstrate potential for self-renewal and lineage conversion. Recent advances in chemical modulation of epigenetic reprogramming, particularly with agents from the family of non-specific DNA methyltransferase (DNMT) inhibitors, such as 5-azacytidine (5-azaC), highlight the feasibility of generating functional, lineage-specific derivatives of GCs or oPSCs without genetic manipulation. Not without significance is also the fact that extended/high-dose 5-azaC-mediated modulation can induce cell senescence or apoptotic/necrotic death. Therefore, dosing must be carefully titrated, which strongly supports a dose- and/or time-dependent mechanism for 5-azaC-based epigenetic modification in treated cells. This study aims to summarize the molecular and functional properties of mammalian GCs and oPSCs, emphasizing their applicability in regenerative medicine and reproductive bioengineering, with a focus on safe, patient-specific cell-based therapies. Full article
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30 pages, 11679 KB  
Article
Procedure for Conducting Inspection Thermographic Tests of Electrical Heating Devices for Railway Turnouts
by Jacek Kukulski, Krzysztof Stypułkowski, Piotr Tomczuk and Piotr Jaskowski
Appl. Sci. 2025, 15(21), 11671; https://doi.org/10.3390/app152111671 - 31 Oct 2025
Viewed by 135
Abstract
The study presents original research focused on improving the reliability and energy efficiency of electric railway turnout heating systems under severe winter conditions. An innovative diagnostic methodology using high-resolution infrared thermography was developed and applied to evaluate heating uniformity and technical performance within [...] Read more.
The study presents original research focused on improving the reliability and energy efficiency of electric railway turnout heating systems under severe winter conditions. An innovative diagnostic methodology using high-resolution infrared thermography was developed and applied to evaluate heating uniformity and technical performance within the Polish railway infrastructure. Field investigations were carried out on operational turnouts at Gdańsk Osowa and Międzylesie stations, covering both conventional EOR systems and the advanced ESAR system. The results demonstrated that the ESAR system effectively prevented ice and snow accumulation while enabling up to a 30% reduction in active power supplied to heating elements, resulting in annual energy savings of approximately 750 kWh per turnout (29% compared with the reference system). Incorporating radiative overlays in ESAR allowed lower average surface temperatures and improved heat distribution efficiency. Temperature and energy indicators confirmed significantly higher performance of ESAR, with annual CO2 emissions reduced by 447.75 kg and air pollutants (SOx, NOx, CO, particulates) by around 30%. The proposed thermographic approach proved to be a non-invasive and efficient diagnostic tool, supporting adaptive control, enhanced operational reliability, and reduced environmental impact of turnout heating systems. Full article
(This article belongs to the Special Issue Research Advances in Rail Transport Infrastructure)
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21 pages, 13574 KB  
Article
Identification of microRNA-Related Target Genes for the Development of Otic Organoids
by Sehee Lee, Sungjin Park, Euyhyun Park, Gi Jung Im and Jiwon Chang
Int. J. Mol. Sci. 2025, 26(21), 10627; https://doi.org/10.3390/ijms262110627 - 31 Oct 2025
Viewed by 185
Abstract
Mammalian hearing loss is typically permanent due to the inability to replace damaged cochlear hair cells. However, the neonatal mice inner ear demonstrates regenerative capacity, with cochlear floor cells proliferating and differentiating into organoids containing new hair cells and supporting cells, yet the [...] Read more.
Mammalian hearing loss is typically permanent due to the inability to replace damaged cochlear hair cells. However, the neonatal mice inner ear demonstrates regenerative capacity, with cochlear floor cells proliferating and differentiating into organoids containing new hair cells and supporting cells, yet the governing molecular mechanisms remain poorly understood. Here, we isolated extracellular vesicles (EVs) from inner ear organoids at proliferation and differentiation stages, characterized their EV miRNA profiles through sequencing, and validated findings using public transcriptomic datasets to elucidate miRNA-mediated regulatory mechanisms during inner ear development. Inner ear organoids were successfully developed from cochlear duct cells, expressing otic progenitor marker SOX2 and hair cell marker Myo7A and demonstrating functional mechano-transduction activity through FM1-43 uptake. Small RNA sequencing identified 35 differentially expressed EV miRNAs between developmental stages. Integrated analysis with public transcriptome datasets revealed 18 genes with significant differential expression, leading to identification of three key regulatory genes—Trp53, Ezh2, and Zbtb4—that exhibited dynamic spatiotemporal expression during inner ear maturation. Pathway analysis demonstrated that these genes are associated with DNA Repair, P53, and Wnt/β-Catenin signaling with remarkable cell-type specificity. Our results demonstrate that EV miRNAs are temporally regulated during organoid development, with predominant downregulation during differentiation. These findings provide crucial insights into developmental mechanisms that could optimize organoid-based models and guide EV miRNA-based therapeutic strategies for hearing restoration. Full article
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17 pages, 3070 KB  
Article
Gonadal Transcriptome Analysis Reveals the lncRNA–mRNA Pair in Sea Cucumber Holothuria leucospilota
by Jing Zhang, Jingwei Yu, Yang Zhang and Meiyao Su
Genes 2025, 16(11), 1293; https://doi.org/10.3390/genes16111293 - 30 Oct 2025
Viewed by 334
Abstract
Background/Objectives: Long non-coding RNA (lncRNA) was structurally similar to mRNAs, yet they could not be translated into proteins. While an increasing number of reports have systematically identified and described lncRNA in model species, information about non-model species remains scarce. Sea cucumber Holothuria leucospilota [...] Read more.
Background/Objectives: Long non-coding RNA (lncRNA) was structurally similar to mRNAs, yet they could not be translated into proteins. While an increasing number of reports have systematically identified and described lncRNA in model species, information about non-model species remains scarce. Sea cucumber Holothuria leucospilota could be used for both medicinal and food purposes, which have high economic value, gradually attracting the attention of researchers. Methods: In this research, we constructed lncRNA library and compared the difference in lncRNA expression profiles between testis and ovary of sea cucumber H. leucospilota. To elucidate the molecular interactions between lncRNA and mRNA, we computationally predicted potential complementary binding sites through analysis of both cis- and trans-acting antisense mechanisms. Subsequent Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses demonstrated that the identified target genes are potentially involved in the regulatory pathways governing gonad development. Results: Quantitative reverse transcription PCR analysis showed that MSTRG.32831.1-sox9 and MSTRG.57315.1-mthfr exhibited a high expression pattern in testis; while MSTRG.11041.1-mafa and MSTRG.11074.1-macf1 showed a high expression pattern in the ovary. Conclusions: Deciphering lncRNA–mRNA expression patterns may uncover fundamental principles governing reproductive regulation in marine invertebrates. This discovery not only deepens understanding in this field but also provides valuable comparative insights for developmental biology. Full article
(This article belongs to the Section RNA)
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