| Literature DB >> 26214133 |
Jonathan Lévy1, Wulfran Cacheux2, Medhi Ait Bara1, Antoine L'Hermitte1, Patricia Lepage3, Marie Fraudeau1, Coralie Trentesaux1, Julie Lemarchand1, Aurélie Durand1, Anne-Marie Crain4, Carmen Marchiol1, Gilles Renault1, Florent Dumont1, Franck Letourneur1, Myriam Delacre5, Alain Schmitt1, Benoit Terris6, Christine Perret1, Mathias Chamaillard5, Jean-Pierre Couty4, Béatrice Romagnolo1.
Abstract
Here, we show that autophagy is activated in the intestinal epithelium in murine and human colorectal cancer and that the conditional inactivation of Atg7 in intestinal epithelial cells inhibits the formation of pre-cancerous lesions in Apc(+/-) mice by enhancing anti-tumour responses. The antibody-mediated depletion of CD8(+) T cells showed that these cells are essential for the anti-tumoral responses mediated by the inhibition of autophagy. We show that Atg7 deficiency leads to intestinal dysbiosis and that the microbiota is required for anticancer responses. In addition, Atg7 deficiency resulted in a stress response accompanied by metabolic defects, AMPK activation and p53-mediated cell-cycle arrest in tumour cells but not in normal tissue. This study reveals that the inhibition of autophagy within the epithelium may prevent the development and progression of colorectal cancer in genetically predisposed patients.Entities:
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Year: 2015 PMID: 26214133 DOI: 10.1038/ncb3206
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.824