Author ORCID Identifier
https://orcid.org/0000-0001-8446-7246
https://orcid.org/0000-0003-3945-5208
N/A
Document Type
Article
Publication Date
2013
Abstract
The oncogenic epithelial–mesenchymal transition (EMT) contributes to tumor progression in various context-dependent ways, including increased metastatic potential, expansion of cancer stem cell subpopulations, chemo-resistance and disease recurrence. One of the hallmarks of EMT is resistance of tumor cells to anoikis. This resistance contributes to metastasis and is a defining property not only of EMT but also of cancer stem cells. Here, we review the mechanistic coupling between EMT and resistance to anoikis. The discussion focuses on several key aspects. First, we provide an update on new pathways that lead from the loss of E-cadherin to anoikis resistance. We then discuss the relevance of transcription factors that are crucial in wound healing in the context of oncogenic EMT. Next, we explore the consequences of the breakdown of cell-polarity complexes upon anoikis sensitivity, through the Hippo, Wnt and transforming growth factor β (TGF-β) pathways, emphasizing points of crossregulation. Finally, we summarize the direct regulation of cell survival genes through EMT-inducing transcription factors, and the roles of the tyrosine kinases focal adhesion kinase (FAK) and TrkB neurotrophin receptor in EMT-related regulation of anoikis. Emerging from these studies are unifying principles that will lead to improvements in cancer therapy by reprogramming sensitivity of anoikis.
Digital Commons Citation
Frisch, Steven M.; Schaller, Michael; and Cieply, Benjamin, "Mechanisms that link the oncogenic epithelial–mesenchymal transition to suppression of anoikis" (2013). Faculty & Staff Scholarship. 228.
https://researchrepository.wvu.edu/faculty_publications/228
Source Citation
Frisch, Steven M.., Schaller, Michael., & Cieply, Benjamin. (2013). Mechanisms That Link The Oncogenic Epithelial–Mesenchymal Transition To Suppression Of Anoikis. Journal of Cell Science, 126(1), 21-29. http://doi.org/10.1242/jcs.120907