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Regulating the stability of TGFβ receptors and Smads
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , Ludwig Institute for Cancer Research.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , Ludwig Institute for Cancer Research.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , Ludwig Institute for Cancer Research.
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Medicinska och farmaceutiska vetenskapsområdet, centrumbildningar mm , Ludwig Institute for Cancer Research.
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2009 (English)In: Cell Research, ISSN 1001-0602, E-ISSN 1748-7838, Vol. 19, no 1, 21-35 p.Article, review/survey (Refereed) Published
Abstract [en]

Transforming growth factor beta (TGFbeta) controls cellular behavior in embryonic and adult tissues. TGFbeta binding to serine/threonine kinase receptors on the plasma membrane activates Smad molecules and additional signaling proteins that together regulate gene expression. In this review, mechanisms and models that aim at explaining the coordination between several components of the signaling network downstream of TGFbeta are presented. We discuss how the activity and duration of TGFbeta receptor/Smad signaling can be regulated by post-translational modifications that affect the stability of key proteins in the pathway. We highlight links between these mechanisms and human diseases, such as tissue fibrosis and cancer.

Place, publisher, year, edition, pages
IBCB, SIBS, CAS , 2009. Vol. 19, no 1, 21-35 p.
Keyword [en]
Lysosome, phosphorylation, proteasome, Smad, SUMO, TGFb, ubiquitin
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-105283DOI: 10.1038/cr.2008.308ISI: 000263287300005PubMedID: 19030025OAI: oai:DiVA.org:uu-105283DiVA: diva2:220981
Available from: 2009-06-03 Created: 2009-06-03 Last updated: 2017-12-13Bibliographically approved

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