Clinical anticancer drug development: targeting the cyclin-dependent kinases.

Clinical anticancer drug development: targeting the cyclin-dependent kinases.
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临床抗癌药物开发:靶向细胞周期蛋白依赖性激酶。

DOI:
10.1038/sj.bjc.6602229
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发表时间:
2005-01-17
影响因子:
8.8
通讯作者:
de Bono, J
de Bono, J
中科院分区:
医学1区
文献类型:
--
作者:
Benson, C;Kaye, S;Workman, P;Garrett, M;Walton, M;de Bono, J

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细胞分裂涉及一个周期性的生化过程,由每个细胞周期必须发生一次的几个逐步反应组成。细胞分裂失调是所有癌症的标志。遗传和表观遗传机制经常导致细胞周期蛋白的表达和/或活性紊乱,包括细胞周期蛋白、细胞周期蛋白依赖性激酶(Cdk)、Cdk抑制剂和检查点控制蛋白。这些蛋白质在细胞周期中的关键性质带来了希望,靶向它们可能导致选择性细胞毒性和有价值的抗癌活性。
Cell division involves a cyclical biochemical process composed of several step-wise reactions that have to occur once per cell cycle. Dysregulation of cell division is a hallmark of all cancers. Genetic and epigenetic mechanisms frequently result in deranged expression and/or activity of cell-cycle proteins including the cyclins, cyclin-dependent kinases (Cdks), Cdk inhibitors and checkpoint control proteins. The critical nature of these proteins in cell cycling raises hope that targeting them may result in selective cytotoxicity and valuable anticancer activity.
DOI: 10.1111/j.1432-1033.1997.t01-2-00527.x
发表时间: 1997-01-15
期刊: EUROPEAN JOURNAL OF BIOCHEMISTRY
影响因子: --
作者:
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发表时间: 2003-01-01
影响因子: 45.3
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发表时间: 2002-12-10
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