Peroxisome proliferator-activated receptor ɑ (PPARɑ)-cytochrome P450 epoxygenases-soluble epoxide hydrolase axis in ER + PR + HER2- breast cancer
Jazyk angličtina Země Japonsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
31823010
DOI
10.1007/s00795-019-00240-7
PII: 10.1007/s00795-019-00240-7
Knihovny.cz E-zdroje
- Klíčová slova
- Arachidonic acid, Breast cancer, CYP epoxygenases, Fibrates, PPARα, Soluble epoxide hydrolase,
- MeSH
- antigen Ki-67 metabolismus MeSH
- cytochrom P-450 CYP2J2 MeSH
- deriváty kyseliny fibrové farmakologie MeSH
- epoxid hydrolasy metabolismus MeSH
- geny erbB-2 * MeSH
- inhibiční koncentrace 50 MeSH
- lidé MeSH
- MFC-7 buňky MeSH
- nádory prsu metabolismus patologie MeSH
- PPAR alfa metabolismus MeSH
- proliferace buněk účinky léků MeSH
- pyrimidiny farmakologie MeSH
- receptory pro estrogeny metabolismus MeSH
- receptory progesteronu metabolismus MeSH
- rozpustnost MeSH
- subcelulární frakce metabolismus MeSH
- systém (enzymů) cytochromů P-450 metabolismus MeSH
- transport proteinů účinky léků MeSH
- viabilita buněk účinky léků MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigen Ki-67 MeSH
- cytochrom P-450 CYP2J2 MeSH
- deriváty kyseliny fibrové MeSH
- epoxid hydrolasy MeSH
- pirinixic acid MeSH Prohlížeč
- PPAR alfa MeSH
- pyrimidiny MeSH
- receptory pro estrogeny MeSH
- receptory progesteronu MeSH
- systém (enzymů) cytochromů P-450 MeSH
Fibrates belong to a group of ligands of peroxisome proliferator-activated receptor alpha (PPARα), which play a role in the regulation of CYP epoxygenases and soluble epoxide hydrolase (sEH), key enzymes in the metabolism of biologically highly active epoxyeicosatrienoic acids (EETs). We demonstrated that low doses of fibrates stimulate proliferation of the MCF7 cell line, while high doses suppress it. The increase in cell proliferation was accompanied by an increase in CYP epoxygenases and decrease in sEH levels. The overall level of PPARα remained same after low-dose fibrate stimulation; however, there was a significant shift of the receptor to the cell nucleus. PPARα expression was further demonstrated by immunohistochemistry in both carcinoma and healthy breast tissue samples both in the cytoplasm and in the nuclei. We have also observed higher nuclear PPARα positivity in tumor tissues. Although our results obtained for MCF7 cells suggest the potential role of PPARα in cell proliferation, we did not find an association between nuclear localization of PPARα and the expression of proliferation marker Ki-67 in tumor tissues. The exact role of PPARα in carcinogenesis still remains unclear.
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