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肿瘤抑制基因。

Tumor suppressor genes.

作者信息

Hinds P W, Weinberg R A

机构信息

Harvard Medical School Department of Pathology, Boston, Massachusetts 02115.

出版信息

Curr Opin Genet Dev. 1994 Feb;4(1):135-41. doi: 10.1016/0959-437x(94)90102-3.

Abstract

The mutation of tumor suppressor genes is thought to contribute to tumor growth by inactivating proteins that normally act to limit cell proliferation. Several tumor suppressor proteins have been identified in recent years, but only two of them, p53 and pRb, are understood in detail. In the past year, a role has become apparent for both of these proteins in transcription and phosphorylation events required for passage of a cell from G1 to S phase. The pRb protein appears to prevent the function of transcription factors and other proteins needed for S phase until its inactivation by cyclin-dependent kinases in late G1. Induction of p53 by DNA damage may act to cause cell cycle arrest or cell death by altering the transcription program of damaged cells. A detailed molecular understanding of these growth regulators is now emerging, and is the subject of this review.

摘要

肿瘤抑制基因的突变被认为是通过使正常情况下限制细胞增殖的蛋白质失活来促进肿瘤生长。近年来已经鉴定出几种肿瘤抑制蛋白,但其中只有两种,即p53和pRb,得到了详细的了解。在过去的一年里,这两种蛋白在细胞从G1期进入S期所需的转录和磷酸化事件中的作用变得明显。pRb蛋白似乎会阻止S期所需的转录因子和其他蛋白质发挥功能,直到其在G1晚期被细胞周期蛋白依赖性激酶失活。DNA损伤诱导p53可能通过改变受损细胞的转录程序来导致细胞周期停滞或细胞死亡。现在正在出现对这些生长调节因子的详细分子理解,这也是本综述的主题。

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