Tumor suppression by Ink4a-Arf:: progress and puzzles

被引:572
作者
Lowe, SW
Sherr, CJ
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] St Jude Childrens Res Hosp, Howard Hughes Med Inst, Dept Genet & Tumor Cell Biol, Memphis, TN 38105 USA
关键词
D O I
10.1016/S0959-437X(02)00013-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The two products of the Ink4a-Arf locus, p16(Ink4a) and p19(Arf) (p14(ARF) in humans), are potent tumor suppressors that regulate the activities of the retinoblastoma protein and the p53 transcription factor. These proteins form part of a signaling network that is disrupted in most, if not all, cancer cells. The Ink4a-Arf locus responds to stress signals, limiting cell proliferation and modulating oncogene-induced apoptosis. Recent evidence emerging from mouse tumor models distinguishes the activities of p16(Ink4a) and p19(Arf) in regulating tumor onset and identifies differences in their responsiveness to drugs.
引用
收藏
页码:77 / 83
页数:7
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