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癌症转移中的RNA甲基腺苷:作用、机制及应用

RNA -Methyladenosine in Cancer Metastasis: Roles, Mechanisms, and Applications.

作者信息

Dang Qin, Shao Bo, Zhou Quanbo, Chen Chen, Guo Yaxin, Wang Guixian, Liu Jinbo, Kan Quancheng, Yuan Weitang, Sun Zhenqiang

机构信息

Department of Colorectal Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.

出版信息

Front Oncol. 2021 Jun 15;11:681781. doi: 10.3389/fonc.2021.681781. eCollection 2021.

DOI:10.3389/fonc.2021.681781
PMID:34211849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8239292/
Abstract

Cancer metastasis is a symptom of adverse prognosis, a prime origin of therapy failure, and a lethal challenge for cancer patients. -methyladenosine (mA), the most prevailing modification in messenger RNAs (mRNAs) and non-coding RNAs (ncRNAs) of higher eukaryotes, has attracted increasing attention. Growing studies have verified the pivotal roles of mA methylation in controlling mRNAs and ncRNAs in diverse physiological processes. Remarkably, recent findings have showed that aberrant methylation of mA-related RNAs could influence cancer metastasis. In this review, we illuminate how mA modifiers act on mRNAs and ncRNAs and modulate metastasis in several cancers, and put forward the clinical application prospects of mA methylation.

摘要

癌症转移是不良预后的症状、治疗失败的主要根源,也是癌症患者面临的致命挑战。N6-甲基腺苷(m6A)是高等真核生物信使核糖核酸(mRNA)和非编码核糖核酸(ncRNA)中最普遍的修饰,已引起越来越多的关注。越来越多的研究证实了m6A甲基化在多种生理过程中对mRNA和ncRNA的调控起着关键作用。值得注意的是,最近的研究结果表明,与m6A相关的RNA异常甲基化可能影响癌症转移。在本综述中,我们阐明了m6A修饰因子如何作用于mRNA和ncRNA并调节几种癌症中的转移,并提出了m6A甲基化的临床应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/0325c3720cce/fonc-11-681781-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/e4c80a9eb979/fonc-11-681781-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/5ac14de262fa/fonc-11-681781-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/0325c3720cce/fonc-11-681781-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/e4c80a9eb979/fonc-11-681781-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/5ac14de262fa/fonc-11-681781-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d0f/8239292/0325c3720cce/fonc-11-681781-g003.jpg

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Int J Mol Sci. 2020 Nov 23;21(22):8855. doi: 10.3390/ijms21228855.
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BMI1 Inhibition Eliminates Residual Cancer Stem Cells after PD1 Blockade and Activates Antitumor Immunity to Prevent Metastasis and Relapse.BMI1 抑制消除 PD1 阻断后的残留癌症干细胞,并激活抗肿瘤免疫以预防转移和复发。
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mA modification-mediated BATF2 acts as a tumor suppressor in gastric cancer through inhibition of ERK signaling.
去甲基化酶AlkB同源物在癌症中的作用。
Front Oncol. 2023 Mar 16;13:1153463. doi: 10.3389/fonc.2023.1153463. eCollection 2023.
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ALKBH1-mediated m A demethylation of METTL3 mRNA promotes the metastasis of colorectal cancer by downregulating SMAD7 expression.ALKBH1 介导的 METTL3 mRNA mA 去甲基化通过下调 SMAD7 表达促进结直肠癌的转移。
Mol Oncol. 2023 Feb;17(2):344-364. doi: 10.1002/1878-0261.13366. Epub 2022 Dec 30.
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