Collagen-derived proline promotes pancreatic ductal adenocarcinoma cell survival under nutrient limited conditions

O. Porta Olivares(Centre National de la Recherche Scientifique), Jared R. Mayers(Massachusetts Institute of Technology), Victoire Gouirand(Centre National de la Recherche Scientifique), Margaret E. Torrence(Massachusetts Institute of Technology), Tristan Gicquel(Centre National de la Recherche Scientifique), Laurence Borge(Centre National de la Recherche Scientifique), Sophie Lac(Centre National de la Recherche Scientifique), Julie Roques(Centre National de la Recherche Scientifique), Marie‐Noëlle Lavaut(Centre National de la Recherche Scientifique), Patrice Berthézène(Centre National de la Recherche Scientifique), Marion Rubis(Centre National de la Recherche Scientifique), Véronique Secq(Centre National de la Recherche Scientifique), Stéphane Garcia(Centre National de la Recherche Scientifique), Vincent Moutardier(Centre National de la Recherche Scientifique), Dominique Lombardo(Inserm), Juan Iovanna(Centre National de la Recherche Scientifique), Richard Tomasini(Centre National de la Recherche Scientifique), Fabienne Guillaumond(Centre National de la Recherche Scientifique), Matthew G. Vander Heiden(Dana-Farber Cancer Institute), Sophie Vasseur(Centre National de la Recherche Scientifique)
Nature Communications
July 7, 2017
Cited by 402Open Access
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Abstract

Tissue architecture contributes to pancreatic ductal adenocarcinoma (PDAC) phenotypes. Cancer cells within PDAC form gland-like structures embedded in a collagen-rich meshwork where nutrients and oxygen are scarce. Altered metabolism is needed for tumour cells to survive in this environment, but the metabolic modifications that allow PDAC cells to endure these conditions are incompletely understood. Here we demonstrate that collagen serves as a proline reservoir for PDAC cells to use as a nutrient source when other fuels are limited. We show PDAC cells are able to take up collagen fragments, which can promote PDAC cell survival under nutrient limited conditions, and that collagen-derived proline contributes to PDAC cell metabolism. Finally, we show that proline oxidase (PRODH1) is required for PDAC cell proliferation in vitro and in vivo. Collectively, our results indicate that PDAC extracellular matrix represents a nutrient reservoir for tumour cells highlighting the metabolic flexibility of this cancer.


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