| Literature DB >> 27622334 |
Lucie Brisson1, Piotr Bański1, Martina Sboarina1, Coralie Dethier1, Pierre Danhier2, Marie-Joséphine Fontenille1, Vincent F Van Hée1, Thibaut Vazeille1, Morgane Tardy1, Jorge Falces1, Caroline Bouzin3, Paolo E Porporato1, Raphaël Frédérick4, Carine Michiels5, Tamara Copetti1, Pierre Sonveaux6.
Abstract
Metabolic adaptability is essential for tumor progression and includes cooperation between cancer cells with different metabolic phenotypes. Optimal glucose supply to glycolytic cancer cells occurs when oxidative cancer cells use lactate preferentially to glucose. However, using lactate instead of glucose mimics glucose deprivation, and glucose starvation induces autophagy. We report that lactate sustains autophagy in cancer. In cancer cells preferentially to normal cells, lactate dehydrogenase B (LDHB), catalyzing the conversion of lactate and NAD(+) to pyruvate, NADH and H(+), controls lysosomal acidification, vesicle maturation, and intracellular proteolysis. LDHB activity is necessary for basal autophagy and cancer cell proliferation not only in oxidative cancer cells but also in glycolytic cancer cells.Entities:
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Year: 2016 PMID: 27622334 DOI: 10.1016/j.ccell.2016.08.005
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743