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PMID: 15734148 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Antagonists of activin signaling: mechanisms and potential biological applications.

Trends in endocrinology and metabolism: TEM ·Vol. 16 ·No. 2 ·2005-03-00 ·Pages 73-8

Harrison CA, Gray PC, Vale WW, Robertson DM

Abstract

Activins are members of the transforming growth factor-beta (TGF-beta) superfamily that control many physiological processes such as cell proliferation and differentiation, immune responses, wound repair and various endocrine activities. Activins elicit these diverse biological responses by signaling via type I and type II receptor serine kinases. Recent studies have revealed details of the roles of inhibin, betaglycan, follistatin and its related protein follistatin-related gene (FLRG), Cripto and BAMBI in antagonizing activin action, and exogenous antagonists against the activin type I (SB-431542 and SB-505124) and type II (activin-M108A) receptors have been developed. Understanding how activin signaling is controlled extracellularly is the first step in providing treatment for wound healing and for disorders such as cachexia and cancer, which result from a deregulated activin pathway.

MeSH Terms
Activins/antagonists & inhibitors,metabolism Animals Cachexia/therapy Hormone Antagonists/pharmacology,therapeutic use Humans Neoplasms/therapy Signal Transduction Wound Healing/drug effects
Chemicals
Hormone Antagonists Activins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Harrison Craig A
Prince Henry's Institute of Medical Research, 246 Clayton Road, Clayton, VIC 3168, Australia. [email protected]
Gray Peter C
Vale Wylie W
Robertson David M
Article Info
Journal
Trends in endocrinology and metabolism: TEM
Abbr.
Trends Endocrinol Metab
ISSN
1043-2760
Published
2005-03-00
Pages
73-8
Language
English
Region
United States
NLM ID
9001516
Subset
IM
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