The role of membrane transporters in ovarian cancer chemoresistance and prognosis
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, přehledy
- Klíčová slova
- Ovarian cancer, chemoresistance, expression, membrane transporters, prognosis,
- MeSH
- antitumorózní látky farmakologie MeSH
- chemorezistence MeSH
- lidé MeSH
- membránové transportní proteiny metabolismus MeSH
- nádorové biomarkery genetika MeSH
- nádory vaječníků farmakoterapie genetika patologie MeSH
- prognóza MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- antitumorózní látky MeSH
- membránové transportní proteiny MeSH
- nádorové biomarkery MeSH
Ovarian cancer has the highest mortality rate of all cancers in women. There is currently no effective method for early diagnosis, limiting the precision of clinical expectations. Predictions of therapeutic efficacy are currently not available either. Specifically, the development of chemoresistance against conventional chemotherapy poses a fundamental complication. Some membrane transporters have been reported to influence chemoresistance, which is often associated with a poor prognosis. Areas covered: The aim of this article is to review the existing information about membrane transporters and their role in both ovarian cancer chemoresistance and its outcomes. We then highlight limitations of current methodologies and suggest alternatives providing avenues for future research. Expert opinion: Membrane transporters play an important role in development of chemoresistance and affect prognosis of ovarian cancer patients; however, due to variations in methodology and in patient populations, their specific roles have yet to be clarified. For further evaluation of the clinical utility of membrane transporters, it is essential to validate results and improve methods for marker assessment across laboratories. A promising area for future research is to identify the genetic variability in potential markers in peripheral blood. These markers would then stratify patients into defined groups for optimal intervention.
b 3rd Faculty of Medicine Charles University Prague Czech Republic
c Biomedical Center Faculty of Medicine in Pilsen Charles University Pilsen Czech Republic
Toxicogenomics Unit National Institute of Public Health Prague Czech Republic
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