m6A修饰调控肿瘤放射抵抗的分子机制

IF 6.4 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Medicine Pub Date : 2025-02-19 DOI:10.1186/s10020-025-01121-9
Ruolin Shen, Zhenyang Jiang, Huanhuan Wang, Zhuangzhuang Zheng, Xin Jiang
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摘要

放射治疗是恶性肿瘤最有效的治疗方法之一。放疗耐药是导致放疗失败和预后不良的主要因素。最近的研究已经阐明了异常n6 -甲基腺苷(m6A)修饰的关键作用,真核细胞中主要的内部mRNA修饰通过破坏基因表达和其他关键的细胞过程来影响癌症的进展。此外,异常的m6A甲基化为肿瘤治疗提供了一个底物;然而,它是否调节肿瘤的放射耐药尚不清楚。甲基化转移酶(writer)、去甲基化转移酶(erase)和甲基化识别蛋白(reader)是在不同肿瘤中通过不同机制调控m6A修饰的三种必需蛋白。本文综述了m6A甲基化的最新研究进展,旨在为克服放射耐药和肿瘤侵袭的方案发展提供新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Molecular mechanisms of m6A modifications regulating tumor radioresistance.

Radiotherapy is one of the most effective treatments for malignant tumors. Radioresistance is a major factor that contributes to radiotherapy failure and poor prognosis. Recent studies have elucidated the pivotal role of aberrant N6-methyladenosine (m6A) modification, the predominant internal mRNA modification in eukaryotic cells, influences cancer progression by disrupting gene expression and other critical cellular processes. Furthermore, aberrant m6A methylation provides a substrate for tumor therapy; however, whether it regulates tumor radioresistance remains unclear. Methylated transferase (writer), demethylated transferase (eraser), and methylated recognition protein (reader) are the three essential proteins that regulate m6A modification via different mechanisms in different tumors. This review summarizes the latest research advances in m6A methylation and aims to provide novel perspectives on the advancement of regimens to overcome radioresistance and tumor invasion.

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来源期刊
Molecular Medicine
Molecular Medicine 医学-生化与分子生物学
CiteScore
8.60
自引率
0.00%
发文量
137
审稿时长
1 months
期刊介绍: Molecular Medicine is an open access journal that focuses on publishing recent findings related to disease pathogenesis at the molecular or physiological level. These insights can potentially contribute to the development of specific tools for disease diagnosis, treatment, or prevention. The journal considers manuscripts that present material pertinent to the genetic, molecular, or cellular underpinnings of critical physiological or disease processes. Submissions to Molecular Medicine are expected to elucidate the broader implications of the research findings for human disease and medicine in a manner that is accessible to a wide audience.
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