Cell Biochemistry and Biophysics, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 7, 2024
Language: Английский
Cell Biochemistry and Biophysics, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 7, 2024
Language: Английский
Future Oncology, Journal Year: 2023, Volume and Issue: 19(35), P. 2369 - 2382
Published: Nov. 1, 2023
Colorectal cancer (CRC) is a significant contributor to mortality worldwide, and the presence of stem cells (CSC) represents major challenge for achieving effective treatment. miRNAs have emerged as critical regulators gene expression, recent studies highlighted their role in regulating stemness therapeutic resistance CRC cells. This review highlights mechanisms CSC development, therapy potential targets CRC. It emphasizes promise novel approach treatment calls further research explore miRNA-based therapies strategies delivering CSCs vivo.
Language: Английский
Citations
4Epigenetics Insights, Journal Year: 2023, Volume and Issue: 16
Published: Jan. 1, 2023
Multiple sclerosis (MS) is a complex autoimmune disorder of the CNS that affects millions people worldwide. The causes disease remain unknown despite extensive efforts to understand it. CircRNAs are unique class endogenous non-coding RNA abundant, stable, conserved, and specifically expressed molecules, making them promising biomarker diseases. This review investigates role circRNA in MS pathogenicity their potential as through comprehensive literature search conducted 8 scientific databases. studies found there differentially circRNAs patients compared healthy controls (HC), this difference even more pronounced different subtypes. Enrichment linkage disequilibrium (LD) blocks harbor MS-associated SNPs suggests these manipulate levels surrounding area, contributing pathogenicity. While shows promise an indicator or for pathology, further research needed fully explore its impact on human biology.
Language: Английский
Citations
4Journal of Translational Medicine, Journal Year: 2024, Volume and Issue: 22(1)
Published: March 16, 2024
Abstract Background Protein cysteine oxidation is substantially involved in various biological and pathogenic processes, but its implications pancreatic cancer development remains poorly understood. Methods results In this study, we performed a global characterization of protein targets PDAC cells through iodoTMT-based quantitative proteomics, which identified over 4300 oxidized sites more than 2100 proteins HPDE6c7 PANC-1 cells. Among them, 1715 residues were shown to be differentially between Also, charged amino acids including aspartate, glutamate lysine significantly overrepresented flanking sequences cysteines. Differentially enriched multiple cancer-related processes signaling pathways. Specifically, the HIF-1 exhibited significant alterations cells, reduced PHD2 human tissues was correlated with lower survival time patients. Conclusion These investigations provided new insights into oxidation-regulated during pathogenesis, might further explored for diagnosis treatment.
Language: Английский
Citations
1Biochemical Pharmacology, Journal Year: 2024, Volume and Issue: 229, P. 116460 - 116460
Published: Aug. 3, 2024
Language: Английский
Citations
1Cell Biochemistry and Biophysics, Journal Year: 2024, Volume and Issue: unknown
Published: Sept. 7, 2024
Language: Английский
Citations
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