4.7 Article

Atg5 Disassociates the V1V0-ATPase to Promote Exosome Production and Tumor Metastasis Independent of Canonical Macroautophagy

Journal

DEVELOPMENTAL CELL
Volume 43, Issue 6, Pages 716-+

Publisher

CELL PRESS
DOI: 10.1016/j.devcel.2017.11.018

Keywords

-

Funding

  1. National Sciences and Engineering Research Council of Canada [436104]
  2. Canadian Cancer Society Research Institute [702978]
  3. Vanier Scholarship from the Canadian Institutes of Health Research
  4. Ministere de l'Enseignement Superieur et de la Recherche
  5. Institut National de la Sante et de la Recherche Medicale, Universite Joseph Fourier
  6. Fondation France Alzheimer
  7. ANR [08-Blanc-0271]
  8. Canadian Institutes of Health Research
  9. Canada Research Chair (Tier II) in RNA Metabolism

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available