Please use this identifier to cite or link to this item: https://doi.org/10.1684/bdc.2010.1206
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dc.titleEpithelial mesenchymal transition during development in fibrosis and in the progression of carcinoma
dc.contributor.authorThiery, J.-P.
dc.contributor.authorChua, K.
dc.contributor.authorSim, W.J.
dc.contributor.authorHuang, R.
dc.date.accessioned2014-11-26T10:00:33Z
dc.date.available2014-11-26T10:00:33Z
dc.date.issued2010-11
dc.identifier.citationThiery, J.-P., Chua, K., Sim, W.J., Huang, R. (2010-11). Epithelial mesenchymal transition during development in fibrosis and in the progression of carcinoma. Bulletin du Cancer 97 (11) : 1285-1295. ScholarBank@NUS Repository. https://doi.org/10.1684/bdc.2010.1206
dc.identifier.issn00074551
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/110813
dc.description.abstractRepublic of Singapore Epithelial mesenchymal transition (EMT) is a fundamental mechanism controlling multiple events during embryonic development. Mesenchymal cells appear transiently in some diploblasts, the most primitive species characterized by two epithelial layers. Since almost 800 million years, EMT has been conserved throughout evolution to control morphogenetic events, such as the formation of the three primary germ layers during gastrulation. Most interestingly, specific molecular pathways have been conserved in many different species to drive EMT. In the animal kingdom, a recurrent theme is that EMT controls the intercellular adhesion machinery and the dynamics of its associated cytoskeleton. EMT pathways are also tightly connected to determination and differentiation programs, and are reactivated in adult tissues following injury or exposure to toxic agents. EMT is now shown to operate during the early stages of carcinoma invasion leading to blood or lymph vessel intravasation of malignant cells. The converse mechanism - mesenchymal- epithelial transition (MET) - then operates at distant sites from the primary tumor to form macrometastases from isolated micrometastatic cells. The mesenchymal-like state of carcinoma confers stemness, protection from cell death, escape from immune response and, most importantly, resistance to conventional and targeted therapies. Our laboratory has designed an EMT high-throughput screen of small molecular weight compounds and biologics in order to establish new therapeutic approaches that interfere with the plasticity of carcinoma cells. New therapeutic interventions are envisioned to delay tumor recurrence. ©John Libbey Eurotext.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1684/bdc.2010.1206
dc.sourceScopus
dc.subjectCarcinoma
dc.subjectEpithelium
dc.subjectGastrulation
dc.subjectInvasion
dc.subjectMesenchyme
dc.subjectMetastasis
dc.subjectOrganogenesis
dc.subjectTargeted therapies
dc.typeReview
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1684/bdc.2010.1206
dc.description.sourcetitleBulletin du Cancer
dc.description.volume97
dc.description.issue11
dc.description.page1285-1295
dc.description.codenBUCAB
dc.identifier.isiut000284827900009
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