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泛素连接酶:细胞周期调控与癌症

Ubiquitin ligases: cell-cycle control and cancer.

作者信息

Nakayama Keiichi I, Nakayama Keiko

机构信息

Department of Molecular and Cellular Biology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Fukuoka 812-8582, Japan.

出版信息

Nat Rev Cancer. 2006 May;6(5):369-81. doi: 10.1038/nrc1881.

Abstract

A driving force of the cell cycle is the activation of cyclin-dependent kinases (CDKs), the activities of which are controlled by the ubiquitin-mediated proteolysis of key regulators such as cyclins and CDK inhibitors. Two ubiquitin ligases, the SKP1-CUL1-F-box-protein (SCF) complex and the anaphase-promoting complex/cyclosome (APC/C), are responsible for the specific ubiquitylation of many of these regulators. Deregulation of the proteolytic system might result in uncontrolled proliferation, genomic instability and cancer. Cumulative clinical evidence shows alterations in the ubiquitylation of cell-cycle regulators in the aetiology of many human malignancies. A better understanding of the ubiquitylation machinery will provide new insights into the regulatory biology of cell-cycle transitions and the development of anti-cancer drugs.

摘要

细胞周期的一个驱动力是细胞周期蛋白依赖性激酶(CDK)的激活,其活性受泛素介导的关键调节因子(如细胞周期蛋白和CDK抑制剂)的蛋白水解作用控制。两种泛素连接酶,即SKP1-CUL1-F-box蛋白(SCF)复合物和后期促进复合物/细胞周期体(APC/C),负责许多这些调节因子的特异性泛素化。蛋白水解系统失调可能导致不受控制的增殖、基因组不稳定和癌症。累积的临床证据表明,在许多人类恶性肿瘤的病因中,细胞周期调节因子的泛素化存在改变。更好地理解泛素化机制将为细胞周期转换的调控生物学和抗癌药物的开发提供新的见解。

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