Cancer cell cycles

被引:4868
作者
Sherr, CJ
机构
[1] Howard Hughes Medical Institute, Department of Tumor Cell Biology, St. Jude Children's Res. Hospital, Memphis, TN 38105
关键词
D O I
10.1126/science.274.5293.1672
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Uncontrolled cell proliferation is the hallmark of cancer, and tumor cells have typically acquired damage to genes that directly regulate their cell cycles. Genetic alterations affecting p16(INK4a) and cyclin D1, proteins that govern phosphorylation of the retinoblastoma protein (RE) and control exit from the G(1) phase of the cell cycle, are so frequent in human cancers that inactivation of this pathway may well be necessary for tumor development. Like the tumor suppressor protein p53, components of this ''RB pathway,'' although not essential for the cell cycle per se, may participate in checkpoint functions that regulate homeostatic tissue renewal throughout life.
引用
收藏
页码:1672 / 1677
页数:6
相关论文
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