Aberrations of the G1- and G1/S-regulating genes in human cancer.

J Bartkova, J Lukas, J Bartek
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引用次数: 96

Abstract

Deregulated cell proliferation is the hallmark of cancer, and convergent data from the fields of cell-cycle research and molecular oncology have revealed the key role played by abnormalities of the cell-cycle control genes in multistep tumorigenesis. Along with the p53-mediated DNA damage checkpoint, the G1-governing pathway of D-type cyclins, their partner cyclin-dependent kinases (Cdk), Cdk inhibitors, and the retinoblastoma protein constitute a functional unit and prominent oncogenic target. We have learned a great deal about the molecular basis of G1 phase progression and G1/S transition, their proto-oncogenic defects, and potential clinical significance including diagnostic and prognostic applications and new approaches to gene therapy of cancer.

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G1-和G1/ s调控基因在人类癌症中的畸变。
失控的细胞增殖是癌症的标志,来自细胞周期研究和分子肿瘤学领域的数据已经揭示了细胞周期控制基因的异常在多步骤肿瘤发生中发挥的关键作用。与p53介导的DNA损伤检查点一起,d型细胞周期蛋白的g1调控通路、它们的伴侣细胞周期蛋白依赖性激酶(Cdk)、Cdk抑制剂和视网膜母细胞瘤蛋白构成了一个功能单元和重要的致癌靶点。我们已经了解了大量关于G1期进展和G1/S转变的分子基础,它们的原癌性缺陷,以及潜在的临床意义,包括诊断和预后应用以及癌症基因治疗的新方法。
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