UCP2 Deficiency Increases Colon Tumorigenesis by Promoting Lipid Synthesis and Depleting NADPH for Antioxidant Defenses.

Clicks: 254
ID: 22721
2019
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Abstract
Colorectal cancer (CRC) is associated with metabolic and redox perturbation. The mitochondrial transporter uncoupling protein 2 (UCP2) controls cell proliferation in vitro through the modulation of cellular metabolism, but the underlying mechanism in tumors in vivo remains unexplored. Using murine intestinal cancer models and CRC patient samples, we find higher UCP2 protein levels in tumors compared to their non-tumoral counterparts. We reveal the tumor-suppressive role of UCP2 as its deletion enhances colon and small intestinal tumorigenesis in AOM/DSS-treated and Apc mice, respectively, and correlates with poor survival in the latter model. Mechanistically, UCP2 loss increases levels of oxidized glutathione and proteins in tumors. UCP2 deficiency alters glycolytic pathways while promoting phospholipid synthesis, thereby limiting the availability of NADPH for buffering oxidative stress. We show that UCP2 loss renders colon cells more prone to malignant transformation through metabolic reprogramming and perturbation of redox homeostasis and could favor worse outcomes in CRC.
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aguilar2019ucp2cell Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Aguilar, Esther;Esteves, Pauline;Sancerni, Tiphaine;Lenoir, Véronique;Aparicio, Thomas;Bouillaud, Frédéric;Dentin, Renaud;Prip-Buus, Carina;Ricquier, Daniel;Pecqueur, Claire;Guilmeau, Sandra;Alves-Guerra, Marie-Clotilde;
Journal Cell reports
Year 2019
DOI
S2211-1247(19)31013-7
URL
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