Contextual determinants of TGFβ action in development, immunity and cancer

被引:800
作者
David, Charles J. [1 ,2 ]
Massague, Joan [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, 1275 York Ave, New York, NY 10021 USA
[2] Tsinghua Univ, Dept Basic Sci, Sch Med, Beijing, Peoples R China
关键词
TRANSFORMING-GROWTH-FACTOR; EPITHELIAL-MESENCHYMAL TRANSITION; EMBRYONIC STEM-CELLS; MASTER TRANSCRIPTION FACTORS; HUMAN PANCREATIC-CANCER; REGULATORY T-CELLS; SIGNALING PATHWAYS; COLORECTAL-CANCER; STRUCTURAL BASIS; SUPER-ENHANCERS;
D O I
10.1038/s41580-018-0007-0
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Few cell signals match the impact of the transforming growth factor-beta (TGF beta) family in metazoan biology. TGF beta cytokines regulate cell fate decisions during development, tissue homeostasis and regeneration, and are major players in tumorigenesis, fibrotic disorders, immune malfunctions and various congenital diseases. The effects of the TGF beta family are mediated by a combinatorial set of ligands and receptors and by a common set of receptor-activated mothers against decapentaplegic homologue (SMAD) transcription factors, yet the effects can differ dramatically depending on the cell type and the conditions. Recent progress has illuminated a model of TGF beta action in which SMADs bind genome-wide in partnership with lineage-determining transcription factors and additionally integrate inputs from other pathways and the chromatin to trigger specific cellular responses. These new insights clarify the operating logic of the TGF beta pathway in physiology and disease.
引用
收藏
页码:419 / 435
页数:17
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