Peters G
Imperial Cancer Research Fund Laboratories, London, UK.
J Cell Sci Suppl. 1994;18:89-96. doi: 10.1242/jcs.1994.supplement_18.13.
The D-type cyclins are expressed during the progression from G0/G1 to S phase in the mammalian cell cycle. There is considerable evidence that they contribute to the development of specific cancers, both in humans and in mouse models. For example, cyclin D1 can be activated by chromosomal translocation, DNA amplification and retroviral integration. Cyclins D1, D2 and D3 preferentially associate with two closely related members of the cyclin-dependent kinase family, Cdk4 and Cdk6 and the various complexes are each capable of phosphorylating the retinoblastoma gene product (pRb), at least in vitro. This suggests that the growth promoting effects of the D-cyclins may be manifest via their interactions with tumour suppressor genes.
D型细胞周期蛋白在哺乳动物细胞周期从G0/G1期向S期进展过程中表达。有大量证据表明,它们在人类和小鼠模型中都对特定癌症的发展有促进作用。例如,细胞周期蛋白D1可通过染色体易位、DNA扩增和逆转录病毒整合而被激活。细胞周期蛋白D1、D2和D3优先与细胞周期蛋白依赖性激酶家族的两个密切相关成员Cdk4和Cdk6结合,并且至少在体外,各种复合物都能够磷酸化视网膜母细胞瘤基因产物(pRb)。这表明D型细胞周期蛋白的促生长作用可能通过它们与肿瘤抑制基因的相互作用而显现出来。