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双刃剑:CDK2AP1 在细胞周期调控和表观遗传调控中的作用。

Double edge: CDK2AP1 in cell-cycle regulation and epigenetic regulation.

机构信息

UCLA School of Dentistry and Dental Research Institute, 10833 Le Conte Ave., 73-017 CHS, Los Angeles, CA 90095, USA.

出版信息

J Dent Res. 2012 Mar;91(3):235-41. doi: 10.1177/0022034511420723. Epub 2011 Aug 24.

DOI:10.1177/0022034511420723
PMID:21865592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3275332/
Abstract

Cancer research has been devoted toward an understanding of the molecular regulation and functional significance of cell-cycle regulators in the pathogenesis and development of cancers. Cyclin-dependent Kinase 2-associated Protein 1 (CDK2AP1) is one such cell-cycle regulator, originally identified as a growth suppressor and a prognostic marker for human oral/head and neck cancers. Functional importance and the molecular mechanism of CDK2AP1-mediated cell-cycle regulation have been documented over the years. Recent progress has shown that CDK2AP1 is a competency factor in embryonic stem cell differentiation. Deletion of CDK2AP1 leads to early embryonic lethality, potentially through altered differentiation capability of embryonic stem cells. More intriguingly, CDK2AP1 exerts its effect on stem cell maintenance/differentiation through epigenetic regulation. Cancer cells and stem cells share common cellular characteristics, most prominently in maintaining high proliferative potential through an unconventional cell-cycle regulatory mechanism. Cross-talk between cellular processes and molecular signaling pathways is frequent in any biological system. Currently, it remains largely elusive how cell-cycle regulation is mechanistically linked to epigenetic control. Understanding the molecular mechanism underlying CDK2AP1-mediated cell-cycle regulation and epigenetic control will set an example for establishing a novel and effective molecular link between these two important regulatory mechanisms.

摘要

癌症研究一直致力于理解细胞周期调控因子在癌症发生和发展中的分子调控和功能意义。细胞周期蛋白依赖性激酶 2 相关蛋白 1(CDK2AP1)就是这样一种细胞周期调控因子,最初被鉴定为人类口腔/头颈部癌症的生长抑制剂和预后标志物。多年来,已经证明 CDK2AP1 介导的细胞周期调控的功能重要性和分子机制。最近的进展表明,CDK2AP1 是胚胎干细胞分化的能力因子。CDK2AP1 的缺失导致早期胚胎致死,可能是通过改变胚胎干细胞的分化能力。更有趣的是,CDK2AP1 通过表观遗传调控对干细胞的维持/分化发挥作用。癌细胞和干细胞具有共同的细胞特征,最明显的是通过一种非传统的细胞周期调控机制维持高增殖潜能。细胞过程和分子信号通路之间的串扰在任何生物系统中都很常见。目前,细胞周期调控如何与表观遗传控制在机制上联系起来在很大程度上仍不清楚。了解 CDK2AP1 介导的细胞周期调控和表观遗传控制的分子机制将为在这两个重要调控机制之间建立新的有效的分子联系树立榜样。

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Hallmarks of cancer: the next generation.癌症的特征:下一代。
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Downregulation of TGF-beta receptor types II and III in oral squamous cell carcinoma and oral carcinoma-associated fibroblasts.口腔鳞状细胞癌和口腔癌相关成纤维细胞中 TGF-β 受体 II 和 III 的下调。
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miR-21 downregulates the tumor suppressor P12 CDK2AP1 and stimulates cell proliferation and invasion.miR-21 下调肿瘤抑制因子 P12 CDK2AP1,从而刺激细胞增殖和侵袭。
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CDK2AP1/DOC-1 is a bona fide subunit of the Mi-2/NuRD complex.细胞周期蛋白依赖性激酶2相关蛋白1/ DOC-1是Mi-2/核小体重塑去乙酰化酶复合物的一个真正亚基。
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