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dc.contributor.authorFifis, T.
dc.contributor.authorTran, B.
dc.contributor.authorSchwab, R.
dc.contributor.authorJohanson, T.
dc.contributor.authorWarner, N.
dc.contributor.authorBarker, N.
dc.contributor.authorVincan, Elizabeth
dc.date.accessioned2017-01-30T12:46:13Z
dc.date.available2017-01-30T12:46:13Z
dc.date.created2015-12-10T04:26:11Z
dc.date.issued2014
dc.identifier.citationFifis, T. and Tran, B. and Schwab, R. and Johanson, T. and Warner, N. and Barker, N. and Vincan, E. 2014. Wnt Signaling Regulation of Tissue Architecture (EMT and MET) and Morphogenesis: Consequences for Colorectal and Liver Cancer. In Wnt Signaling in Development and Disease: Molecular Mechanisms and Biological Functions, 315-328: Wiley Blackwell.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/24997
dc.identifier.doi10.1002/9781118444122.ch24
dc.description.abstract

© 2014 John Wiley & Sons, Inc. The different branches of the Wnt signaling pathway were first characterized in developmental contexts, but in recent times, each branch has been implicated in tumor growth and progression. This chapter exemplifies this link between development and cancer by focusing on two Wnt-driven cancers, colorectal cancer (CRC) and hepatocellular carcinoma (HCC). It focuses on the processes of epithelial-to-mesenchymal transition (EMT) and the reverse transition, mesenchymal-to-epithelial transition (MET), both fundamental mechanisms of tumor metastasis and morphogenesis. HCC shares many parallels with CRC with respect to the involvement of Wnt signaling in cancer initiation and progression.

dc.publisherWiley Blackwell
dc.titleWnt Signaling Regulation of Tissue Architecture (EMT and MET) and Morphogenesis: Consequences for Colorectal and Liver Cancer
dc.typeBook Chapter
dcterms.source.startPage315
dcterms.source.endPage328
dcterms.source.titleWnt Signaling in Development and Disease: Molecular Mechanisms and Biological Functions
dcterms.source.isbn9781118444160
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusFulltext not available


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