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. 2014 Feb;4(2):186-99.
doi: 10.1158/2159-8290.CD-13-0520. Epub 2013 Dec 3.

Epithelial-to-mesenchymal Transition Rewires the Molecular Path to PI3K-dependent Proliferation

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Epithelial-to-mesenchymal Transition Rewires the Molecular Path to PI3K-dependent Proliferation

Megan B Salt et al. Cancer Discov. .
Free article

Abstract

Tumors showing evidence of epithelial-to-mesenchymal transition (EMT) have been associated with metastasis, drug resistance, and poor prognosis. Heterogeneity along the EMT spectrum is observed between and within tumors. To develop effective therapeutics, a mechanistic understanding of how EMT affects the molecular requirements for proliferation is needed. We found that although cells use phosphoinositide 3-kinase (PI3K) for proliferation in both the epithelial and mesenchymal states, EMT rewires the mechanism of PI3K pathway activation. In epithelial cells, autocrine ERBB3 activation maintains PI3K signaling, whereas after EMT, downregulation of ERBB3 disrupts autocrine signaling to PI3K. Loss of ERBB3 leads to reduced serum-independent proliferation after EMT that can be rescued through reactivation of PI3K by enhanced signaling from p110α, ERBB3 reexpression, or growth factor stimulation. In vivo, we demonstrate that PIK3CA expression is upregulated in mesenchymal tumors with low levels of ERBB3. This study defines how ERBB3 downregulation after EMT affects PI3K-dependent proliferation.

Significance: This study describes a mechanism through which EMT transition alters the proliferative potential of cells by modulating ERBB3 expression. Furthermore, it demonstrates the potential for multiple molecular routes to drive proliferation in different cell states, illustrating how changes in EMT status can rewire signaling upstream of cell proliferation.

Comment in

  • EMT twists the road to PI3K.
    Niederst MJ, Benes CH. Niederst MJ, et al. Cancer Discov. 2014 Feb;4(2):149-51. doi: 10.1158/2159-8290.CD-13-1030. Cancer Discov. 2014. PMID: 24501304 Free PMC article.

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