Role of RUNX Family Members in G1 Restriction-Point Regulation

被引:4
|
作者
Lee, Jung-Won [1 ]
Bae, Suk-Chul [1 ]
机构
[1] Chungbuk Natl Univ, Coll Med, Dept Biochem, Cheongju 28644, South Korea
基金
新加坡国家研究基金会;
关键词
BRD; PcG complex; restriction point; RUNX; TrxG complex; CDK INHIBITORS; POLYCOMB; PROTEIN; BRD2; P53;
D O I
10.14348/molcells.2019.0319
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
When cells are stimulated by growth factors, they make a critical choice in early G(1) phase: proceed forward to S phase, remain in G(1), or revert to G(0) phase. Once the critical decision is made, cells execute a fixed program independently of extracellular signals. The specific stage at which the critical decision is made is called the restriction point or R-point. The existence of the R-point raises a major question: what is the nature of the molecular machinery that decides whether or not a cell in G(1) will continue to advance through the cell cycle or exit from the cell cycle? The R-point program is perturbed in nearly all cancer cells. Therefore, exploring the nature of the R-point decision-making machinery will provide insight into how cells consult extracellular signals and intracellular status to make an appropriate R-point decision, as well into the development of cancers. Recent studies have shown that expression of a number of immediate early genes is associated with the R-point decision, and that the decision-making program constitutes an oncogene surveillance mechanism. In this review, we briefly summarize recent findings regarding the mechanisms underlying the context-dependent R-point decision.
引用
收藏
页码:182 / 187
页数:6
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