| Literature DB >> 29257951 |
Huishan Guo1, Maneka Chitiprolu1, Luc Roncevic1, Charlotte Javalet2, Fiona J Hemming2, My Tran Trung1, Lingrui Meng1, Elyse Latreille1, Christiano Tanese de Souza3, Danielle McCulloch1, R Mitchell Baldwin1, Rebecca Auer3, Jocelyn Côté1, Ryan Charles Russell1, Rémy Sadoul2, Derrick Gibbings4.
Abstract
Autophagy and autophagy-related genes (Atg) have been attributed prominent roles in tumorigenesis, tumor growth, and metastasis. Extracellular vesicles called exosomes are also implicated in cancer metastasis. Here, we demonstrate that exosome production is strongly reduced in cells lacking Atg5 and Atg16L1, but this is independent of Atg7 and canonical autophagy. Atg5 specifically decreases acidification of late endosomes where exosomes are produced, disrupting the acidifying V1V0-ATPase by removing a regulatory component, ATP6V1E1, into exosomes. The effect of Atg5 on exosome production promotes the migration and in vivo metastasis of orthotopic breast cancer cells. These findings uncover mechanisms controlling exosome release and identify means by which autophagy-related genes can contribute to metastasis in autophagy-independent pathways.Entities:
Keywords: LC3; V(1)V(0)-ATPase; acidification; autophagy; cancer; endosome; exosomes; extracellular vesicles; multivesicular body; tumor
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Year: 2017 PMID: 29257951 DOI: 10.1016/j.devcel.2017.11.018
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270