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EMT-induced stemness and tumorigenicity are fueled by the EGFR/Ras pathway.

ABSTRACT: Recent studies have revealed that differentiated epithelial cells would acquire stem cell-like and tumorigenic properties following an Epithelial-Mesenchymal Transition (EMT). However, the signaling pathways that participate in this novel mechanism of tumorigenesis have not been fully characterized. In Runx3 (-/-) p53 (-/-) murine gastric epithelial (GIF-14) cells, EMT-induced plasticity is reflected in the expression of the embryonal proto-oncogene Hmga2 and Lgr5, an exclusive gastrointestinal stem cell marker. Here, we report the concurrent activation of an EGFR/Ras gene expression signature during TGF-?1-induced EMT in GIF-14 cells. Amongst the altered genes was the induction of Egfr, which corresponded with a delayed sensitization to EGF treatment in GIF-14. Co-treatment with TGF-?1 and EGF or the expression of exogenous KRas led to increased Hmga2 or Lgr5 expression, sphere initiation and colony formation in soft agar assay. Interestingly, the gain in cellular plasticity/tumorigenicity was not accompanied by increased EMT. This uncoupling of EMT and the induction of plasticity reveals an involvement of distinct signaling cues, whereby the EGFR/Ras pathway specifically promotes stemness and tumorigenicity in EMT-altered GIF-14 cells. These data show that the EGFR/Ras pathway requisite for the sustenance of gastric stem cells in vivo and in vitro is involved in the genesis and promotion of EMT-induced tumor-initiating cells.

SUBMITTER: Voon DC

PROVIDER: S-EPMC3741305 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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EMT-induced stemness and tumorigenicity are fueled by the EGFR/Ras pathway.

Voon Dominic Chih-Cheng DC Wang Huajing H Koo Jason Kin Wai JK Chai Juin Hsien JH Hor Yit Teng YT Tan Tuan Zea TZ Chu Yeh-Shiu YS Mori Seiichi S Ito Yoshiaki Y

PloS one 20130812 8

Recent studies have revealed that differentiated epithelial cells would acquire stem cell-like and tumorigenic properties following an Epithelial-Mesenchymal Transition (EMT). However, the signaling pathways that participate in this novel mechanism of tumorigenesis have not been fully characterized. In Runx3 (-/-) p53 (-/-) murine gastric epithelial (GIF-14) cells, EMT-induced plasticity is reflected in the expression of the embryonal proto-oncogene Hmga2 and Lgr5, an exclusive gastrointestinal ...[more]

PMID: 23950932

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EMT-induced stemness and tumorigenicity are fueled by the EGFR/Ras pathway.

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EMT-induced stemness and tumorigenicity are fueled by the EGFR/Ras pathway.

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