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RB作为衰老和肿瘤抑制的关键调节因子发挥作用。

RB functions as a key regulator of senescence and tumor suppression.

作者信息

Gao Minling, Li Haiou, Zhang Jinfang

机构信息

Department of Hepatobiliary and Pancreatic Surgery, Medical Research Institute, Frontier Science Center of Immunology and Metabolism, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, China; Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan 430071, China; Hubei Key Laboratory of Tumor Biological Behavior/Hubei Provincial Clinical Research Center for Cancer, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, China.

Department of Dermatology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan 430071, China.

出版信息

Semin Cancer Biol. 2025 Feb;109:1-7. doi: 10.1016/j.semcancer.2024.11.004. Epub 2024 Dec 13.

DOI:10.1016/j.semcancer.2024.11.004
PMID:39675647
Abstract

The Retinoblastoma (RB) protein is crucial for regulating gene transcription and chromatin remodeling, impacting cell cycle progression, cellular senescence, and tumorigenesis. Cellular senescence, characterized by irreversible growth arrest and phenotypic alterations, serves as a vital barrier against tumor progression and age-related diseases. RB is crucial in mediating senescence and tumor suppression by modulating the RB-E2F pathway and cross talking with other key senescence effectors such as p53 and p16. The interplay between RB-mediated cell cycle arrest and cellular senescence offers critical insights into tumorigenesis and potential therapeutic strategies. Leveraging RB-mediated senescence presents promising opportunities for cancer therapy, including novel approaches in tumor immunotherapy designed to enhance treatment efficacy. This review highlights recent advancements in the RB signaling pathway, focusing on its roles in cellular senescence and tumor suppression, and discusses its potential to improve tumor management and clinical outcomes.

摘要

视网膜母细胞瘤(RB)蛋白对于调节基因转录和染色质重塑至关重要,影响细胞周期进程、细胞衰老和肿瘤发生。细胞衰老以不可逆的生长停滞和表型改变为特征,是对抗肿瘤进展和与年龄相关疾病的重要屏障。RB通过调节RB-E2F通路并与其他关键衰老效应因子(如p53和p16)相互作用,在介导衰老和肿瘤抑制中起关键作用。RB介导的细胞周期停滞与细胞衰老之间的相互作用为肿瘤发生和潜在治疗策略提供了重要见解。利用RB介导的衰老为癌症治疗带来了有前景的机会,包括旨在提高治疗效果的肿瘤免疫治疗新方法。本综述重点介绍了RB信号通路的最新进展,聚焦于其在细胞衰老和肿瘤抑制中的作用,并讨论了其改善肿瘤管理和临床结果的潜力。

相似文献

1
RB functions as a key regulator of senescence and tumor suppression.RB作为衰老和肿瘤抑制的关键调节因子发挥作用。
Semin Cancer Biol. 2025 Feb;109:1-7. doi: 10.1016/j.semcancer.2024.11.004. Epub 2024 Dec 13.
2
E2FBP1 antagonizes the p16(INK4A)-Rb tumor suppressor machinery for growth suppression and cellular senescence by regulating promyelocytic leukemia protein stability.E2FBP1 通过调节早幼粒细胞白血病蛋白稳定性拮抗 p16(INK4A)-Rb 肿瘤抑制因子机制以抑制细胞生长和诱导细胞衰老。
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The histone demethylase Jarid1b (Kdm5b) is a novel component of the Rb pathway and associates with E2f-target genes in MEFs during senescence.组蛋白去甲基化酶 Jarid1b(Kdm5b)是 Rb 通路的一个新组成部分,在衰老过程中与 MEFs 中的 E2f 靶基因相关联。
PLoS One. 2011;6(9):e25235. doi: 10.1371/journal.pone.0025235. Epub 2011 Sep 27.
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The p16INK4a-RB pathway: molecular link between cellular senescence and tumor suppression.p16INK4a-RB 通路:细胞衰老与肿瘤抑制之间的分子联系。
J Med Invest. 2004 Aug;51(3-4):146-53. doi: 10.2152/jmi.51.146.
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Distinct roles for p107 and p130 in Rb-independent cellular senescence.p107和p130在不依赖Rb的细胞衰老中的不同作用。
Cell Cycle. 2008 May 1;7(9):1262-8. doi: 10.4161/cc.7.9.5945. Epub 2008 Mar 7.
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Rb protein is essential to the senescence-associated heterochromatic foci formation induced by HMGA2 in primary WI38 cells.Rb 蛋白对于 HMGA2 在原代 WI38 细胞中诱导的衰老相关异染色质焦点形成是必需的。
J Genet Genomics. 2013 Aug 20;40(8):391-8. doi: 10.1016/j.jgg.2013.05.007. Epub 2013 Jun 12.
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Dissecting the unique role of the retinoblastoma tumor suppressor during cellular senescence.解析视网膜母细胞瘤抑癌基因在细胞衰老过程中的独特作用。
Cancer Cell. 2010 Apr 13;17(4):376-87. doi: 10.1016/j.ccr.2010.01.023.
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The role of the NORE1A tumor suppressor in Oncogene-Induced Senescence.NORE1A肿瘤抑制因子在癌基因诱导的衰老中的作用。
Cancer Lett. 2017 Aug 1;400:30-36. doi: 10.1016/j.canlet.2017.04.030. Epub 2017 Apr 26.
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Ras Regulates Rb via NORE1A.Ras通过NORE1A调节视网膜母细胞瘤蛋白。
J Biol Chem. 2016 Feb 5;291(6):3114-23. doi: 10.1074/jbc.M115.697557. Epub 2015 Dec 16.
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Cooperative interactions between RB and p53 regulate cell proliferation, cell senescence, and apoptosis in human vascular smooth muscle cells from atherosclerotic plaques.RB与p53之间的协同相互作用调节动脉粥样硬化斑块中人类血管平滑肌细胞的细胞增殖、细胞衰老和细胞凋亡。
Circ Res. 1998 Apr 6;82(6):704-12. doi: 10.1161/01.res.82.6.704.

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