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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Added by amaraver
Group name EquipeAM
Item Type Journal Article
Title c-RAF Ablation Induces Regression of Advanced Kras/Trp53 Mutant Lung Adenocarcinomas by a Mechanism Independent of MAPK Signaling
Creator Sanclemente et al.
Author Manuel Sanclemente
Author Sarah Francoz
Author Laura Esteban-Burgos
Author Emilie Bousquet-Mur
Author Magdolna Djurec
Author Pedro P. Lopez-Casas
Author Manuel Hidalgo
Author Carmen Guerra
Author Matthias Drosten
Author Monica Musteanu
Author Mariano Barbacid
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 Cancer Cell
Volume 33
Issue 2
Pages 217-228.e4
Date Feb 12, 2018
Journal Abbr Cancer Cell
Language eng
DOI 10.1016/j.ccell.2017.12.014
ISSN 1878-3686
Library Catalog PubMed
Extra PMID: 29395869
Tags c-RAF, Kras oncogene, lung cancer, MAPK signaling, mouse models of cancer, original, therapy strategy
Date Added 2018/11/15 - 17:04:53
Date Modified 2019/05/16 - 10:49:09
Notes and Attachments PubMed entry (Attachment)


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