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前列腺癌中的毫安调节器:分子基础与临床前景

The mA regulators in prostate cancer: molecular basis and clinical perspective.

作者信息

Cao Yu, Jia Man, Duan Chunyan, Yang Zhihui, Cheng Bo, Wang Ronghao

机构信息

Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Southwest Medical University, Luzhou, China.

Department of Pathology, The Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.

出版信息

Front Pharmacol. 2024 Aug 29;15:1448872. doi: 10.3389/fphar.2024.1448872. eCollection 2024.

DOI:10.3389/fphar.2024.1448872
PMID:39268470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11391310/
Abstract

Prostate cancer (PCa) is the second leading cause of cancer-related death among men in western countries. Evidence has indicated the significant role of the androgen receptor (AR) as the main driving factor in controlling the development of PCa, making androgen receptor inhibition (ARI) therapy a pivotal management approach. In addition, AR independent signaling pathways also contribute to PCa progression. One such signaling pathway that has garnered our attention is N6-Methyladenosine (mA) signaling, which refers to a chemical modification on RNA with crucial roles in RNA metabolism and disease progression, including PCa. It is important to comprehensively summarize the role of each individual mA regulator in PCa development and understand its interaction with AR signaling. This review aims to provide a thorough summary of the involvement of mA regulators in PCa development, shedding light on their upstream and downstream signaling pathways. This summary sets the stage for a comprehensive review that would benefit the scientific community and clinical practice by enhancing our understanding of the biology of mA regulators in the context of PCa.

摘要

前列腺癌(PCa)是西方国家男性癌症相关死亡的第二大主要原因。有证据表明,雄激素受体(AR)作为控制PCa发展的主要驱动因素发挥着重要作用,这使得雄激素受体抑制(ARI)疗法成为一种关键的治疗方法。此外,AR非依赖性信号通路也有助于PCa的进展。其中一个引起我们关注的信号通路是N6-甲基腺苷(m6A)信号通路,它指的是RNA上的一种化学修饰,在RNA代谢和包括PCa在内的疾病进展中起着关键作用。全面总结每个m6A调节因子在PCa发展中的作用并了解其与AR信号通路的相互作用非常重要。本综述旨在全面总结m6A调节因子在PCa发展中的参与情况,阐明其上游和下游信号通路。这一总结为全面综述奠定了基础,通过加强我们对PCa背景下m6A调节因子生物学的理解,将使科学界和临床实践受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/2c13d8ba54bb/fphar-15-1448872-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/82a5aae0a386/fphar-15-1448872-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/46924d9e9e65/fphar-15-1448872-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/d623abb811a0/fphar-15-1448872-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/2752f287bdf1/fphar-15-1448872-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/64c462f3d7e7/fphar-15-1448872-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/2c13d8ba54bb/fphar-15-1448872-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/82a5aae0a386/fphar-15-1448872-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/46924d9e9e65/fphar-15-1448872-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/d623abb811a0/fphar-15-1448872-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/2752f287bdf1/fphar-15-1448872-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/64c462f3d7e7/fphar-15-1448872-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e04/11391310/2c13d8ba54bb/fphar-15-1448872-g006.jpg

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本文引用的文献

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ZFHX3 acts as a tumor suppressor in prostate cancer by targeting FTO-mediated mA demethylation.锌指同源框蛋白3(ZFHX3)通过靶向FTO介导的N6-甲基腺苷(m6A)去甲基化作用,在前列腺癌中发挥肿瘤抑制因子的功能。
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Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
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YTHDF2 protein stabilization by the deubiquitinase OTUB1 promotes prostate cancer cell proliferation via PRSS8 mRNA degradation.
去泛素化酶OTUB1对YTHDF2蛋白的稳定作用通过PRSS8 mRNA降解促进前列腺癌细胞增殖。
J Biol Chem. 2024 Apr;300(4):107152. doi: 10.1016/j.jbc.2024.107152. Epub 2024 Mar 9.
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The FTO Mediated N6-Methyladenosine Modification of DDIT4 Regulation with Tumorigenesis and Metastasis in Prostate Cancer.FTO介导的DDIT4的N6-甲基腺苷修饰与前列腺癌的肿瘤发生和转移调控
Research (Wash D C). 2024 Feb 21;7:0313. doi: 10.34133/research.0313. eCollection 2024.
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Epigenetic regulation by quercetin: a comprehensive review focused on its biological mechanisms.槲皮素的表观遗传调控:聚焦其生物学机制的综述
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RNA N6-methyladenosine-modified-binding protein YTHDF1 promotes prostate cancer progression by regulating androgen function-related gene TRIM68.RNA N6-甲基腺苷修饰结合蛋白 YTHDF1 通过调节雄激素功能相关基因 TRIM68 促进前列腺癌的进展。
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Glucocorticoid Receptor (GR) Activation Is Associated with Increased cAMP/PKA Signaling in Castration-Resistant Prostate Cancer.糖皮质激素受体(GR)激活与去势抵抗性前列腺癌中 cAMP/PKA 信号的增加有关。
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Circ_0082878 contributes to prostate cancer progression via the miR-455-3p/WTAP axis.环状 RNA 0082878 通过 miR-455-3p/WTAP 轴促进前列腺癌进展。
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Development of a specific and potent IGF2BP1 inhibitor: A promising therapeutic agent for IGF2BP1-expressing cancers.开发一种特异性和高效的 IGF2BP1 抑制剂:一种有前途的针对 IGF2BP1 表达癌症的治疗药物。
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