Glycol porphyrin derivatives and temoporfin elicit resistance to photodynamic therapy by different mechanisms
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28295025
PubMed Central
PMC5353759
DOI
10.1038/srep44497
PII: srep44497
Knihovny.cz E-zdroje
- MeSH
- chemorezistence genetika MeSH
- ethylenglykoly aplikace a dávkování chemie MeSH
- fotochemoterapie MeSH
- fotosenzibilizující látky aplikace a dávkování chemie MeSH
- genový knockdown MeSH
- glykoly chemie MeSH
- lidé MeSH
- mesoporfyriny aplikace a dávkování chemie MeSH
- MFC-7 buňky MeSH
- myši MeSH
- nádory mléčné žlázy u zvířat farmakoterapie genetika patologie MeSH
- P-glykoprotein genetika MeSH
- paclitaxel škodlivé účinky MeSH
- porfyriny aplikace a dávkování chemie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- ethylenglykoly MeSH
- fotosenzibilizující látky MeSH
- glykoly MeSH
- mesoporfyriny MeSH
- P-glykoprotein MeSH
- paclitaxel MeSH
- porfyriny MeSH
- temoporfin MeSH Prohlížeč
The development of drug resistance is a major problem which often occurs during anticancer chemotherapies. Photodynamic therapy (PDT) has been studied as an alternative treatment modality for drug-resistant tumors, however the question of resistance to PDT and potential cross-resistance with chemotherapy has yet to be fully answered. To investigate the mechanism of resistance to PDT, we developed an in vitro experimental model system in a mouse mammary carcinoma cell line 4T1. We used two ethylene glycol derivatives of tetraphenylporphyrin, and tetraphenylchlorin derivative, temoporfin, as photosensitizers (PS). PDT-resistant clones were obtained by exposure to a set concentration of PS followed by irradiation with increasing light doses. PDT resistance to soluble glycol porphyrins was mediated mainly by increased drug efflux through ABCB1 (P-glycoprotein) as we demonstrated by specific ABCB1 knockdown experiments, which in turn rescued the sensitivity of resistant cells to PDT. In contrast, resistance raised to temoporfin, which is generally more lipophilic than glycol porphyrins, elicited mechanism based on sequestration of the drug to lysosomes. The resistance that is acquired from a particular PS could be overcome by using a different PS, which is not susceptible to the same mechanism(s) of resistance. Elucidation of the underlying mechanisms in various types of resistance might facilitate improvements in PDT treatment design.
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