The Roles of Mitogen-Activated Protein Kinase Pathways in TGF-β-Induced Epithelial-Mesenchymal Transition
Author(s) -
Ting Gui,
Yujing Sun,
Aiko Shimokado,
Yasuteru Muragaki
Publication year - 2012
Publication title -
journal of signal transduction
Language(s) - English
Resource type - Journals
eISSN - 2090-1739
pISSN - 2090-1747
DOI - 10.1155/2012/289243
Subject(s) - mapk/erk pathway , epithelial–mesenchymal transition , smad , microbiology and biotechnology , crosstalk , signal transduction , protein kinase a , mesenchymal stem cell , transforming growth factor , motility , kinase , cancer research , medicine , biology , metastasis , cancer , physics , optics
The mitogen-activated protein kinase (MAPK) pathway allows cells to interpret external signals and respond appropriately, especially during the epithelial-mesenchymal transition (EMT). EMT is an important process during embryonic development, fibrosis, and tumor progression in which epithelial cells acquire mesenchymal, fibroblast-like properties and show reduced intercellular adhesion and increased motility. TGF- β signaling is the first pathway to be described as an inducer of EMT, and its relationship with the Smad family is already well characterized. Studies of four members of the MAPK family in different biological systems have shown that the MAPK and TGF- β signaling pathways interact with each other and have a synergistic effect on the secretion of additional growth factors and cytokines that in turn promote EMT. In this paper, we present background on the regulation and function of MAPKs and their cascades, highlight the mechanisms of MAPK crosstalk with TGF- β signaling, and discuss the roles of MAPKs in EMT.
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