Epithelial-mesenchymal transition: from molecular mechanisms, redox regulation to implications in human health and disease
- PMID: 19903090
- DOI: 10.1089/ars.2009.2737
Epithelial-mesenchymal transition: from molecular mechanisms, redox regulation to implications in human health and disease
Abstract
Epithelial to mesenchymal transition (EMT) is a fundamental process, paradigmatic of the concept of cell plasticity, that leads epithelial cells to lose their polarization and specialized junctional structures, to undergo cytoskeleton reorganization, and to acquire morphological and functional features of mesenchymal-like cells. Although EMT has been originally described in embryonic development, where cell migration and tissue remodeling have a primary role in regulating morphogenesis in multicellular organisms, recent literature has provided evidence suggesting that the EMT process is a more general biological process that is also involved in several pathophysiological conditions, including cancer progression and organ fibrosis. This review offers first a comprehensive introduction to describe major relevant features of EMT, followed by sections dedicated on those signaling mechanisms that are known to regulate or affect the process, including the recently proposed role for oxidative stress and reactive oxygen species (ROS). Current literature data involving EMT in both physiological conditions (i.e., embryogenesis) and major human diseases are then critically analyzed, with a special final focus on the emerging role of hypoxia as a relevant independent condition able to trigger EMT.
Similar articles
-
LIM-domain proteins in transforming growth factor β-induced epithelial-to-mesenchymal transition and myofibroblast differentiation.Cell Signal. 2012 Apr;24(4):819-25. doi: 10.1016/j.cellsig.2011.12.004. Epub 2011 Dec 11. Cell Signal. 2012. PMID: 22182513 Review.
-
Molecular characterization of TGFbeta-induced epithelial-mesenchymal transition in normal finite lifespan human mammary epithelial cells.Biochem Biophys Res Commun. 2010 Sep 3;399(4):659-64. doi: 10.1016/j.bbrc.2010.07.138. Epub 2010 Aug 5. Biochem Biophys Res Commun. 2010. PMID: 20691661
-
Regulation of epithelial to mesenchymal transition by bone morphogenetic proteins.Cell Signal. 2013 Dec;25(12):2856-62. doi: 10.1016/j.cellsig.2013.09.012. Epub 2013 Sep 14. Cell Signal. 2013. PMID: 24044921 Review.
-
EMT and oxidative stress: a bidirectional interplay affecting tumor malignancy.Antioxid Redox Signal. 2012 Jun 1;16(11):1248-63. doi: 10.1089/ars.2011.4280. Epub 2011 Nov 2. Antioxid Redox Signal. 2012. PMID: 21929373 Review.
-
The epithelial-mesenchymal transition: new insights in signaling, development, and disease.J Cell Biol. 2006 Mar 27;172(7):973-81. doi: 10.1083/jcb.200601018. J Cell Biol. 2006. PMID: 16567498 Free PMC article. Review.
Cited by
-
Regulation of stem cell populations by microRNAs.Adv Exp Med Biol. 2013;786:329-51. doi: 10.1007/978-94-007-6621-1_18. Adv Exp Med Biol. 2013. PMID: 23696365 Free PMC article. Review.
-
The Promising Therapeutic Approaches for Radiation-Induced Pulmonary Fibrosis: Targeting Radiation-Induced Mesenchymal Transition of Alveolar Type II Epithelial Cells.Int J Mol Sci. 2022 Nov 30;23(23):15014. doi: 10.3390/ijms232315014. Int J Mol Sci. 2022. PMID: 36499337 Free PMC article. Review.
-
Febuxostat inhibits TGF‑β1‑induced epithelial‑mesenchymal transition via downregulation of USAG‑1 expression in Madin‑Darby canine kidney cells in vitro.Mol Med Rep. 2019 Mar;19(3):1694-1704. doi: 10.3892/mmr.2019.9806. Epub 2019 Jan 2. Mol Med Rep. 2019. PMID: 30628645 Free PMC article.
-
The Mu opioid receptor promotes opioid and growth factor-induced proliferation, migration and Epithelial Mesenchymal Transition (EMT) in human lung cancer.PLoS One. 2014 Mar 24;9(3):e91577. doi: 10.1371/journal.pone.0091577. eCollection 2014. PLoS One. 2014. PMID: 24662916 Free PMC article.
-
Oxidative Stress and Skin Fibrosis.Curr Pathobiol Rep. 2014;2(4):257-267. doi: 10.1007/s40139-014-0062-y. Curr Pathobiol Rep. 2014. PMID: 25401052 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources