TGF-β Family Signaling in the Control of Cell Proliferation and Survival

被引:403
|
作者
Zhang, Yun [1 ,2 ]
Alexander, Peter B. [1 ]
Wang, Xiao-Fan [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[2] Whitehead Inst Biomed Res, 9 Cambridge Ctr, Cambridge, MA 02142 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2017年 / 9卷 / 04期
基金
美国国家卫生研究院;
关键词
TRANSFORMING-GROWTH-FACTOR; MAMMARY EPITHELIAL-CELLS; BREAST-CANCER CELLS; BONE MORPHOGENETIC PROTEIN; DEPENDENT KINASE INHIBITOR; FAS-MEDIATED APOPTOSIS; CYCLE ARREST; C-MYC; PREMATURE SENESCENCE; SMAD PROTEINS;
D O I
10.1101/cshperspect.a022145
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The transforming growth factor beta (TGF-beta) family controls many fundamental aspects of cellular behavior. With advances in the molecular details of the TGF-beta signaling cascade and its cross talk with other signaling pathways, we nowhave a more coherent understanding of the cytostatic program induced by TGF-beta. However, the molecular mechanisms are still largely elusive for other cellular processes that are regulated by TGF-beta and determine a cell's proliferation and survival, apoptosis, dormancy, autophagy, and senescence. The difficulty in defining TGF-beta's roles partly stems from the context-dependent nature of TGF-beta signaling. Here, we review our current understanding and recent progress on the biological effects of TGF-b at the cellular level, with the hope of providing a framework for understanding how cells respond to TGF-beta signals in specific contexts, and why disruption of such mechanisms may result in different human diseases including cancer.
引用
收藏
页数:22
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