| Literature DB >> 29337187 |
Benedikt Warth1, Philipp Raffeiner2, Ana Granados3, Tao Huan3, Mingliang Fang4, Erica M Forsberg3, H Paul Benton3, Laura Goetz5, Caroline H Johnson6, Gary Siuzdak7.
Abstract
Recently, the palbociclib/letrozole combination therapy was granted accelerated US FDA approval for the treatment of estrogen receptor (ER)-positive breast cancer. Since the underlying metabolic effects of these drugs are yet unknown, we investigated their synergism at the metabolome level in MCF-7 cells. As xenoestrogens interact with the ER, we additionally aimed at deciphering the impact of the phytoestrogen genistein and the estrogenic mycotoxin zearalenone. A global metabolomics approach was applied to unravel metabolite and pathway modifications. The results clearly showed that the combined effects of palbociclib and letrozole on cellular metabolism were far more pronounced than that of each agent alone and potently influenced by xenoestrogens. This behavior was confirmed in proliferation experiments and functional assays. Specifically, amino acids and central carbon metabolites were attenuated, while higher abundances were observed for fatty acids and most nucleic acid-related metabolites. Interestingly, exposure to model xenoestrogens appeared to counteract these effects.Entities:
Keywords: CDK4/6 inhibitor; Ibrance; bioactive food constituents; combinatory chemotherapy; drug-exposome interactions; endocrine-disrupting chemicals; mTOR; metabolic pathway analysis; soy isoflavone; untargeted metabolomics
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Year: 2018 PMID: 29337187 PMCID: PMC5856613 DOI: 10.1016/j.chembiol.2017.12.010
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116