Matters of context guide future research in TGFβ superfamily signaling

被引:48
作者
Akhurst, Rosemary J. [1 ,2 ]
Padgett, Richard W. [3 ,4 ]
机构
[1] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94158 USA
[3] Rutgers State Univ, Waksman Inst, Dept Mol Biol & Biochem, Piscataway, NJ 08854 USA
[4] Rutgers State Univ, Canc Inst New Jersey, Piscataway, NJ 08854 USA
关键词
TRANSFORMING-GROWTH-FACTOR; FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; EPITHELIAL-MESENCHYMAL TRANSITION; MOLECULAR-WEIGHT COMPLEX; RGM PROTEIN DRAG-1; I RECEPTOR; SUPPRESSES METASTASIS; HUMAN-PLATELETS; LIGAND TRAP; CELL FATE;
D O I
10.1126/scisignal.aad0416
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 highly conserved wiring of the SMAD-dependent transforming growth factor beta (TGF beta) superfamily signaling pathway has been mapped over the last 20 years after molecular discovery of its component parts. Numerous alternative TGF beta-activated signaling pathways that elicit SMAD-independent biological responses also exist. However, the molecular mechanisms responsible for the renowned context dependency of TGFb signaling output remains an active and often confounding area of research, providing a prototype relevant to regulation of other signaling pathways. Highlighting discoveries presented at the 9th FASEB meeting, The TGF beta Superfamily: Signaling in Development and Disease (July 12-17th 2015 in Snowmass, Colorado), this Review outlines research into the rich contextual nature of TGFb signaling output and offers clues for therapeutic advances.
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页数:10
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