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Data · dataset · 2023

Cooperative pro-tumorigenic adaptation to oncogenic RAS through epithelial to mesenchymal plasticity

Listed in Teesside University Research Data Repository

In breast cancers, aberrant activation of the RAS/MAPK pathway is strongly associated with mesenchymal features and stemness traits, suggesting an interplay between this mitogenic signaling pathway and epithelial-mesenchymal plasticity (EMP).

Description

By using inducible models of human mammary epithelial cells, we demonstrate herein that the oncogenic activation of RAS promotes ZEB1-dependent EMP, which is necessary for malignant transformation.

Notably, EMP is triggered by the secretion of pro-inflammatory cytokines from neighboring RAS-activated senescent cells, with a prominent role for IL-6 and IL-1. Our data contrast with the common view of cellular senescence as a tumor suppressive mechanism and EMP as a process promoting late stages of tumor progression in response to signals from the tumor microenvironment. Indeed, we highlighted here a pro-tumorigenic cellular cooperation of RAS-activated mammary epithelial cells, which leverages on oncogene-induced senescence and EMP to trigger cellular reprogramming and tumor initiation.

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Where it is published

Catalogue records · 1

Topics

Inferred from text
Cancer 65% · Oncology and carcinogenesis 71%
Provenance · 1 source records, 13 field assertions
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Teesside University Research Data Repositoryoai:data.mendeley.com/gcy3g4g42j.27 d agoJSON v1
FieldAssertionExtractorEvidence
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