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癌症中RNA mC修饰的表观转录组学机制及其影响

Epitranscriptomic mechanisms and implications of RNA mC modification in cancer.

作者信息

Mao Zhonghao, Tian Yan, Wu Lisha, Zhang Yu

机构信息

Department of Gynecology, Xiangya Hospital, Central South University, Changsha, China.

Gynecological Oncology Research and Engineering Center of Hunan Province, Changsha, China.

出版信息

Theranostics. 2025 Jul 25;15(16):8404-8428. doi: 10.7150/thno.112332. eCollection 2025.


DOI:10.7150/thno.112332
PMID:40860147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12374585/
Abstract

Cancer is an extremely complex disease characterized by abnormal cell growth due to genetic and environmental factors. With the rise of the field of epigenetic transcriptomics, 5-methylcytidine (mC) modification has been identified as one of the most common chemical modifications occurring in various RNA types. The writers, erasers, and readers of mC modification regulate cancer initiation, progression, and therapeutic responses, such as the proliferation, metastasis, angiogenesis, metabolic reprogramming, immune escape, and therapeutic resistance of tumour cells, by regulating RNA stability, translation, nuclear export, and splicing processes. In this review, we elucidate the biological process of mC modification, summarize the abnormal expression of RNA-modifying proteins (RMPs) in common malignant tumours, explore their functional effects on malignant hallmarks of cancer and molecular mechanisms, and prospect the potential clinical application value of mC.

摘要

癌症是一种极其复杂的疾病,其特征是由于遗传和环境因素导致细胞异常生长。随着表观遗传转录组学领域的兴起,5-甲基胞苷(mC)修饰已被确定为各种RNA类型中最常见的化学修饰之一。mC修饰的写入器、擦除器和读取器通过调节RNA稳定性、翻译、核输出和剪接过程,来调控癌症的发生、发展和治疗反应,如肿瘤细胞的增殖、转移、血管生成、代谢重编程、免疫逃逸和治疗耐药性。在这篇综述中,我们阐明了mC修饰的生物学过程,总结了常见恶性肿瘤中RNA修饰蛋白(RMP)的异常表达,探讨了它们对癌症恶性特征的功能影响和分子机制,并展望了mC潜在的临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/e1e08160baf2/thnov15p8404g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/cf95a9aa4096/thnov15p8404g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/58a5b2eb9f75/thnov15p8404g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/854e9aa75a9d/thnov15p8404g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/f3257c28b5e3/thnov15p8404g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/e1e08160baf2/thnov15p8404g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/cf95a9aa4096/thnov15p8404g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/58a5b2eb9f75/thnov15p8404g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/854e9aa75a9d/thnov15p8404g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/f3257c28b5e3/thnov15p8404g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea0/12374585/e1e08160baf2/thnov15p8404g005.jpg

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Epitranscriptomic mechanisms and implications of RNA mC modification in cancer.

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本文引用的文献

[1]
ALYREF Promotes Progression of Intrahepatic Cholangiocarcinoma through Increasing the Level of Isocitrate Dehydrogenase 1 in an m5C-Dependent Manner.

Mol Cell Biol. 2025

[2]
The mC methyltransferase NSUN2 promotes progression of acute myeloid leukemia by regulating serine metabolism.

Cell Rep. 2025-5-27

[3]
FOXA1-dependent NSUN2 facilitates the advancement of prostate cancer by preserving TRIM28 mRNA stability in a m5C-dependent manner.

NPJ Precis Oncol. 2025-5-3

[4]
STING aggravates ferroptosis-dependent myocardial ischemia-reperfusion injury by targeting GPX4 for autophagic degradation.

Signal Transduct Target Ther. 2025-4-25

[5]
ETV4/ALYREF-mediated glycolytic metabolism through PKM2 enhances resistance to ferroptosis and promotes the development of intrahepatic cholangiocarcinoma.

Cancer Metab. 2025-4-22

[6]
YBX1 promotes 5-Fluorouracil resistance in gastric cancer via m5C-dependent ATG9A mRNA stabilization through autophagy.

Oncogene. 2025-4-18

[7]
LINC02167 stabilizes KSR1 mRNA in an mC-dependent manner to regulate the ERK/MAPK signaling pathway and promotes colorectal cancer metastasis.

J Exp Clin Cancer Res. 2025-4-15

[8]
Novel molecular mechanisms of immune evasion in hepatocellular carcinoma: NSUN2-mediated increase of SOAT2 RNA methylation.

Cancer Commun (Lond). 2025-4-14

[9]
Aberrant CircTMEM45A Facilitates Inflammatory Progression of Esophageal Squamous Cell Carcinoma through m5C-Mediated NLRP3 Activation.

Cancer Res. 2025-7-15

[10]
The cGAS‒STING pathway in cancer immunity: mechanisms, challenges, and therapeutic implications.

J Hematol Oncol. 2025-4-5

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