Research Paper Volume 4, Issue 7 pp 480—498
Metabolomic fingerprint reveals that metformin impairs one-carbon metabolism in a manner similar to the antifolate class of chemotherapy drugs
- 1 Translational Research Laboratory, Catalan Institute of Oncology, Girona, Spain
- 2 Girona Biomedical Research Institute, Girona, Spain
- 3 Department of Analytical Chemistry, Faculty of Sciences, University of Granada, Granada, Spain
- 4 Research and Development of Functional Food Centre (CIDAF), Health Science Technological Park, Granada, Spain
- 5 Clinical Research Unit, Catalan Institute of Oncology, Girona, Spain
- 6 Molecular and Cellular Biology Institute (IBMC), Miguel Hernández University, Elche, Spain
- 7 Unitat de Recerca Biomèdica (URB-CRB), Institut d'Investigació Sanitària Pere Virgili (IISPV), Universitat Rovira i Virgili, Reus, Catalonia, Spain
Received: June 21, 2012 Accepted: July 21, 2012 Published: July 22, 2012
https://doi.org/10.18632/aging.100472How to Cite
Abstract
Metabolomic fingerprint of breast cancer cells treated with the antidiabetic drug metformin revealed a significant accumulation of 5-formimino-tetrahydrofolate, one of the tetrahydrofolate forms carrying activated one-carbon units that are essential for the de novo synthesis of purines and pyrimidines. De novo synthesis of glutathione, a folate-dependent pathway interconnected with one-carbon metabolism was concomitantly depleted in response to metformin. End-product reversal studies demonstrated that thymidine alone leads to a significant but incomplete protection from metformin's cytostatic effects. The addition of the substrate hypoxanthine for the purine salvage pathway produces major rightward shifts in metformin's growth inhibition curves. Metformin treatment failed to activate the DNA repair protein ATM kinase and the metabolic tumor suppressor AMPK when thymidine and hypoxanthine were present in the extracellular milieu. Our current findings suggest for the first time that metformin can function as an antifolate chemotherapeutic agent that induces the ATM/AMPK tumor suppressor axis secondarily following the alteration of the carbon flow through the folate-related one-carbon metabolic pathways.