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N6-甲基腺苷在前列腺癌中的功能和作用机制(综述)。

Functions and mechanisms of N6‑methyladenosine in prostate cancer (Review).

机构信息

Wuxi Medical College, Jiangnan University, Wuxi, Jiangsu 214122, P.R. China.

Department of Burns and Plastic Surgery, The Affiliated Hospital of Jiangnan University, Wuxi, Jiangsu 214122, P.R. China.

出版信息

Mol Med Rep. 2022 Sep;26(3). doi: 10.3892/mmr.2022.12796. Epub 2022 Jul 20.

DOI:10.3892/mmr.2022.12796
PMID:35856412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9364137/
Abstract

Prostate cancer (PCa) has long been a major public health problem affecting men worldwide. Even with treatment, it can develop into castration‑resistant PCa. With the continuous advancement in epigenetics, researchers have explored N6‑methyladenosine (mA) in search of a more effective and lasting treatment for PCa. mA is widely distributed in mammalian cells and influences various aspects of mRNA metabolism. Recently, it has been associated with the development or suppression of various types of cancer, including PCa. This review summarizes the recent findings on mA regulation and its functions and mechanisms in cells, focusing on the various functional proteins operating within mA in PCa cells. Moreover, the potential clinical value of exploiting mA modification as an early diagnostic marker in PCa diagnosis and therapeutics was discussed. mA may also be used as an indicator to evaluate treatment outcome and prognosis.

摘要

前列腺癌(PCa)一直是一个全球性的重大公共卫生问题,影响着全世界的男性。即使经过治疗,它也可能发展为去势抵抗性 PCa。随着表观遗传学的不断发展,研究人员一直在探索 N6-甲基腺苷(mA),以期为 PCa 找到更有效和持久的治疗方法。mA 广泛分布于哺乳动物细胞中,影响 mRNA 代谢的各个方面。最近,它与各种类型癌症的发展或抑制有关,包括 PCa。本综述总结了 mA 调控及其在细胞中的功能和机制的最新发现,重点介绍了在 PCa 细胞中发挥作用的各种功能蛋白。此外,还讨论了利用 mA 修饰作为 PCa 诊断和治疗的早期诊断标志物的潜在临床价值。mA 也可以用作评估治疗效果和预后的指标。

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本文引用的文献

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Hsa_circ_0003258 promotes prostate cancer metastasis by complexing with IGF2BP3 and sponging miR-653-5p.hsa_circ_0003258 通过与 IGF2BP3 复合物并海绵吸附 miR-653-5p 促进前列腺癌转移。
Mol Cancer. 2022 Jan 5;21(1):12. doi: 10.1186/s12943-021-01480-x.
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Regulation of AR mRNA translation in response to acute AR pathway inhibition.急性雄激素受体信号通路抑制后雄激素受体 mRNA 翻译的调控。
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Demethyltransferase FTO alpha-ketoglutarate dependent dioxygenase (FTO) regulates the proliferation, migration, invasion and tumor growth of prostate cancer by modulating the expression of melanocortin 4 receptor (MC4R).
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去甲基化酶 FTOα-酮戊二酸依赖双加氧酶(FTO)通过调节黑素皮质素 4 受体(MC4R)的表达来调节前列腺癌的增殖、迁移、侵袭和肿瘤生长。
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METTL3-mediated m6A modification of KIF3C-mRNA promotes prostate cancer progression and is negatively regulated by miR-320d.METTL3 介导的 KIF3C-mRNA m6A 修饰促进前列腺癌进展,并受 miR-320d 的负调控。
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Characterization of the m6A-Associated Tumor Immune Microenvironment in Prostate Cancer to Aid Immunotherapy.m6A 相关肿瘤免疫微环境在前列腺癌中的特征分析以辅助免疫治疗。
Front Immunol. 2021 Aug 31;12:735170. doi: 10.3389/fimmu.2021.735170. eCollection 2021.
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Silencing of METTL3 effectively hinders invasion and metastasis of prostate cancer cells.沉默 METTL3 可有效抑制前列腺癌细胞的侵袭和转移。
Theranostics. 2021 Jun 11;11(16):7640-7657. doi: 10.7150/thno.61178. eCollection 2021.
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The FTO mA demethylase inhibits the invasion and migration of prostate cancer cells by regulating total mA levels.FTO mA 去甲基酶通过调节总 mA 水平抑制前列腺癌细胞的侵袭和迁移。
Life Sci. 2021 Apr 15;271:119180. doi: 10.1016/j.lfs.2021.119180. Epub 2021 Feb 8.
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