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Serine Deprivation Enhances Antineoplastic Activity of Biguanides

2014; American Association for Cancer Research; Volume: 74; Issue: 24 Linguagem: Inglês

10.1158/0008-5472.can-14-2643-t

1538-7445

Simon‐Pierre Gravel, Laura Hulea, Nader Toban, Elena Birman, Marie‐José Blouin, Mahvash Zakikhani, Yunhua Zhao, Ivan Topisirović, Julie St‐Pierre, Michaël Pollak,

Cancer, Hypoxia, and Metabolism

Metformin, a biguanide widely used in the treatment of type II diabetes, clearly exhibits antineoplastic activity in experimental models and has been reported to reduce cancer incidence in diabetics. There are ongoing clinical trials to evaluate its antitumor properties, which may relate to its fundamental activity as an inhibitor of oxidative phosphorylation. Here, we show that serine withdrawal increases the antineoplastic effects of phenformin (a potent biguanide structurally related to metformin). Serine synthesis was not inhibited by biguanides. Instead, metabolic studies indicated a requirement for serine to allow cells to compensate for biguanide-induced decrease in oxidative phosphorylation by upregulating glycolysis. Furthermore, serine deprivation modified the impact of metformin on the relative abundance of metabolites within the citric acid cycle. In mice, a serine-deficient diet reduced serine levels in tumors and significantly enhanced the tumor growth-inhibitory actions of biguanide treatment. Our results define a dietary manipulation that can enhance the efficacy of biguanides as antineoplastic agents that target cancer cell energy metabolism.