TGF-j3 signaling in health and disease

被引:342
作者
Massague, Joan [1 ]
Sheppard, Dean [2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Canc Biol & Genet Program, New York, NY 10065 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94158 USA
关键词
GROWTH-FACTOR-BETA; BONE MORPHOGENETIC PROTEIN; OF-FUNCTION MUTATIONS; DEPENDENT KINASE INHIBITOR; BREAST-CANCER METASTASIS; ANTI-MULLERIAN HORMONE; REGULATORY T-CELLS; GENOMIC CHARACTERIZATION; ACROMESOMELIC DYSPLASIA; TARGETED DISRUPTION;
D O I
10.1016/j.cell.2023.07.036
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
The TGF-j3 regulatory system plays crucial roles in the preservation of organismal integrity. TGF-j3 signaling controls metazoan embryo development, tissue homeostasis, and injury repair through coordinated effects on cell proliferation, phenotypic plasticity, migration, metabolic adaptation, and immune surveillance of multiple cell types in shared ecosystems. Defects of TGF-j3 signaling, particularly in epithelial cells, tissue fibro-blasts, and immune cells, disrupt immune tolerance, promote inflammation, underlie the pathogenesis of fibrosis and cancer, and contribute to the resistance of these diseases to treatment. Here, we review how TGF-j3 coordinates multicellular response programs in health and disease and how this knowledge can be leveraged to develop treatments for diseases of the TGF-j3 system.
引用
收藏
页码:4007 / 4037
页数:31
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