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PMID: 18620071 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Ups and downs: the STAT1:STAT3 seesaw of Interferon and gp130 receptor signalling.

Seminars in cell & developmental biology ·Vol. 19 ·No. 4 ·2008-08-00 ·Pages 351-9

Regis G, Pensa S, Boselli D, Novelli F, Poli V

Abstract

Downstream of cytokine or growth factor receptors, STAT3 counteracts inflammation and promotes cell survival/proliferation and immune tolerance while STAT1 inhibits proliferation and favours innate and adaptive immune responses. STAT1 and STAT3 activation are reciprocally regulated and perturbation in their balanced expression or phosphorylation levels may re-direct cytokine/growth factor signals from proliferative to apoptotic, or from inflammatory to anti-inflammatory. Here we review the functional canonical and non-canonical effects of STAT1/3 activation and discuss the hypothesis that perturbation of their expression and/or activation levels may provide novel therapeutic strategies in different clinical settings and particularly in cancer.

MeSH Terms
Animals Cell Proliferation Cell Survival Cytokine Receptor gp130/metabolism Cytokines/metabolism Humans Inflammation/metabolism Interferons/metabolism Neoplasms/metabolism STAT1 Transcription Factor/metabolism STAT3 Transcription Factor/metabolism Signal Transduction/physiology
Chemicals
Cytokines STAT1 Transcription Factor STAT3 Transcription Factor Cytokine Receptor gp130 Interferons
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Regis Gabriella
Molecular Biotechnology Center, University of Turin, via Nizza 52, 10126 Turin, Italy. gabriella.regis@unito.it
Pensa Sara
Boselli Daniela
Novelli Francesco
Poli Valeria
Article Info
Journal
Seminars in cell & developmental biology
Abbr.
Semin Cell Dev Biol
ISSN
1084-9521
Published
2008-08-00
Epub
2008-00-22
Pages
351-9
Language
English
Region
England
NLM ID
9607332
Subset
IM
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