Answers are grounded in this paper and cite their sources.
Review outlines how RNA 5-methylcytosine modifications influence cancer progression and treatment strategies.
RNA modifications serve notable roles in various biological processes, with >170 identified modifications.These modifications increase the complexity of RNA species by influencing their tertiary structure, biogenesis, localization and function.The combination of high-throughput detection technologies and corresponding analytical workflows provides a precise 5-methylcytosine (m 5 C) landscape, helping to elucidate its biological functions.The m 5 C methylation occurs in coding and non-coding RNAs and is dynamically regulated by related enzymes, including methyltransferases (writers), demethylases (erasers) and binding proteins (readers).m 5 c is involved in various physiological functions and regulates the progression of numerous types of tumors.Aberrant m 5 c RNA modifications contribute to the proliferation, migration and drug resistance of cancer cells, suggesting that targeting aberrant posttranscriptional modifications in cancer cells may hold promise as an efficient therapy for tumors.The present review systematically outlines the regulatory components of m 5 C modification, emphasizing their dynamic regulatory roles in RNA metabolism and function.The mechanisms by which m 5 C modification promotes tumor progression through the regulation of cancer cell proliferation, migration and drug resistance are summarized.The present review proposes that targeting abnormal m 5 C modifications could serve as a novel strategy for cancer treatment, offering new research directions in oncology.Contents 1. Introduction 2. Writers, erasers and readers for m 5 C modification 3. Methods for detecting m 5 C modification 4. Modification of m 5 C in mRNA 5. Modification of m 5 C in ncRNAs 6. Conclusions
No takes yet. Share an insight, caveat, or question.
Jiang et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: