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TGF-β SIGNAL TRANSDUCTION

Annual Review of Biochemistry · 1998 · Vol. 67(1) · pp. 753–791
Joan Massagué

Abstract

The transforming growth factor beta (TGF-beta) family of growth factors control the development and homeostasis of most tissues in metazoan organisms. Work over the past few years has led to the elucidation of a TGF-beta signal transduction network. This network involves receptor serine/threonine kinases at the cell surface and their substrates, the SMAD proteins, which move into the nucleus, where they activate target gene transcription in association with DNA-binding partners. Distinct repertoires of receptors, SMAD proteins, and DNA-binding partners seemingly underlie, in a cell-specific manner, the multifunctional nature of TGF-beta and related factors. Mutations in these pathways are the cause of various forms of human cancer and developmental disorders.

TGF-β signaling in diseasesGenetic factors in colorectal cancerPancreatic and Hepatic Oncology ResearchSignal transductionTransduction (biophysics)R-SMADTransforming growth factorCell biologyBiologyGeneticsReceptorBiochemistryGrowth factor

MeSH terms

Biological TransportDNA-Binding ProteinsGene Expression RegulationHumansNeoplasmsSignal TransductionTrans-ActivatorsTransforming Growth Factor betaProtein Serine-Threonine KinasesReceptors, Transforming Growth Factor betaGenetic Diseases, InbornSmad1 Protein
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