The Logic of Tgfbeta Signaling.
From: Cancer Biology and Genetics Program, Howard Hughes Medical Institute, Memorial Sloan-Kettering Cancer Center, P.O. Box 116, 1275 York Avenue, New York, NY 10021, USA. j-massague@ski.mskcc.org
FEBS letters
- Publish Date: May 2006
- ISSN: 0014-5793
- Volume: 580
- Issue: 12
- Pages: 2811-20
- Medium: Print
- Language: English
- Citation (JAMA): Massagué Joan, Gomis Roger R, et al. The Logic of Tgfbeta Signaling.. FEBS Lett. May 2006;580:2811-20
Abstract
The identification of the TGFbeta cytokine signaling pathway, including membrane receptor serine/threonine kinases and Smad transcription factors as their substrates, has allowed the delineation of a process for conversion of these signals into programs of gene activation and repression that underlie critical cell fate and developmental decisions. The deconstruction of one of these responses - the cell cycle arrest response - into its elemental molecular parts has shed light into the mechanisms used by tumors to evade surveillance and cause metastasis.
Mesh Headings (Keywords): Animals, Humans, Signal Transduction, Transcription, Genetic, Transforming Growth Factor beta
Check for Full Text / PubMed Unique Identifier (PMID): 16678165
This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.
Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.
The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.
