c-RAF Ablation Induces Regression of Advanced Kras/Trp53 Mutant Lung Adenocarcinomas by a Mechanism Independent of MAPK Signaling. Academic Article uri icon

Overview

abstract

  • A quarter of all solid tumors harbor KRAS oncogenes. Yet, no selective drugs have been approved to treat these malignancies. Genetic interrogation of the MAPK pathway revealed that systemic ablation of MEK or ERK kinases in adult mice prevent tumor development but are unacceptably toxic. Here, we demonstrate that ablation of c-RAF expression in advanced tumors driven by KrasG12V/Trp53 mutations leads to significant tumor regression with no detectable appearance of resistance mechanisms. Tumor regression results from massive apoptosis. Importantly, systemic abrogation of c-RAF expression does not inhibit canonical MAPK signaling, hence, resulting in limited toxicities. These results are of significant relevance for the design of therapeutic strategies to treat K-RAS mutant cancers.

publication date

  • January 27, 2018

Research

keywords

  • Adenocarcinoma of Lung
  • Genes, ras
  • Mutation
  • Proto-Oncogene Proteins c-raf
  • ras Proteins

Identity

Scopus Document Identifier

  • 85040973845

Digital Object Identifier (DOI)

  • 10.1016/j.ccell.2017.12.014

PubMed ID

  • 29395869

Additional Document Info

volume

  • 33

issue

  • 2