The Role of PPARs in MDR - a lesson from embryonic development
Jazyk angličtina Země Slovensko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
19469651
DOI
10.4149/neo_2009_04_279
Knihovny.cz E-zdroje
- MeSH
- embryo savčí metabolismus MeSH
- embryonální vývoj fyziologie MeSH
- lidé MeSH
- mnohočetná léková rezistence * MeSH
- P-glykoproteiny metabolismus MeSH
- receptory aktivované proliferátory peroxizomů fyziologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Názvy látek
- P-glykoproteiny MeSH
- receptory aktivované proliferátory peroxizomů MeSH
One of the most important features of embryonic cells is their resistence to xenobiotics, which provides a natural protection for embryos against these potentially harmful molecules. In this way, embryo cells resemble cancer cells and thus understanding the basis of this phenomenon may contribute to overcoming the multi-drug-resistance (MDR) of some tumours. Peroxisome proliferator-activated receptors (PPARs) are steroid nuclear receptors that regulate diverse biological processes such as lipid and carbohydrate metabolism, development, differentiation, apoptosis, neoplastic transformation, inflammation and regeneration of tissues. Recently it has been found that they may also regulate the expression of some MDR proteins. In this article we summarise the main known relationships between some MDR pumps and three isoforms of PPAR receptors (PPAR-alpha, PPAR-beta/delta, PPAR-gamma). We hypothesize that regulation of MDR proteins by PPAR ligands in embryos could lead to the improvement of cancer treatment.
Citace poskytuje Crossref.org
Differential expression of ABC transporters (MDR1, MRP1, BCRP) in developing human embryos