| Literature DB >> 26804918 |
Étienne Audet-Walsh1, David J Papadopoli2, Simon-Pierre Gravel1, Tracey Yee2, Gaëlle Bridon1, Maxime Caron3, Guillaume Bourque4, Vincent Giguère5, Julie St-Pierre6.
Abstract
Reprogramming of cellular metabolism plays a central role in fueling malignant transformation, and AMPK and the PGC-1α/ERRα axis are key regulators of this process. The intersection of gene-expression and binding-event datasets for breast cancer cells shows that activation of AMPK significantly increases the expression of PGC-1α/ERRα and promotes the binding of ERRα to its cognate sites. Unexpectedly, the data also reveal that ERRα, in concert with PGC-1α, negatively regulates the expression of several one-carbon metabolism genes, resulting in substantial perturbations in purine biosynthesis. This PGC-1α/ERRα-mediated repression of one-carbon metabolism promotes the sensitivity of breast cancer cells and tumors to the anti-folate drug methotrexate. These data implicate the PGC-1α/ERRα axis as a core regulatory node of folate cycle metabolism and further suggest that activators of AMPK could be used to modulate this pathway in cancer.Entities:
Keywords: AMPK; folate; metabolic reprogramming; methotrexate; nuclear receptor
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Year: 2016 PMID: 26804918 DOI: 10.1016/j.celrep.2015.12.086
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423