| Identifikační kód |
RIV/00216208:11160/22:10450893 |
| Název v anglickém jazyce |
Encorafenib Acts as a Dual-Activity Chemosensitizer through Its Inhibitory Effect on ABCC1 Transporter In Vitro and Ex Vivo |
| Druh |
J - Recenzovaný odborný článek (Jimp, Jsc a Jost) |
| Poddruh |
J/A - Článek v odborném periodiku je obsažen v databázi Web of Science společností Thomson Reuters s příznakem „Article“, „Review“ nebo „Letter“ (Jimp) |
| Jazyk |
eng - angličtina |
| Vědní obor |
30104 - Pharmacology and pharmacy |
| Rok uplatnění |
2022 |
| Kód důvěrnosti údajů |
S - Úplné a pravdivé údaje o výsledku nepodléhající ochraně podle zvláštních právních předpisů. |
| Počet výskytů výsledku |
4 |
| Popis výsledku v anglickém jazyce |
Encorafenib (LGX818, trade name Braftovi), a novel BRAF inhibitor, has been approved for the treatment of melanoma and colorectal cancer. In the present work, we evaluated possible en-corafenib's antagonistic effects on the pharmacokinetic mechanisms of multidrug resistance (MDR) as well as its perpetrator role in drug interactions. Firstly, encorafenib potently inhibited the efflux function of ABCC1 transporter in drug accumulation assays, while moderate and null interaction levels were recorded for ABCB1 and ABCG2, respectively. In contrast, the mRNA expression levels of all the tested transporters were not altered by encorafenib. In the drug combination studies, we found that daunorubicin and topotecan resistances were synergistically attenuated by the en-corafenib-mediated interaction in A431-ABCC1 cells. Notably, further experiments in ex vivo pa-tient-derived explants confirmed the MDR-modulating ability of encorafenib. Advantageously, the overexpression of tested drug efflux transporters failed to hinder the antiproliferative activity of encorafenib. In addition, no significant modulation of CYP3A4 enzyme's activity by encorafenib was observed. In conclusion, our work indicated that encorafenib can act as an effective chemo-sensitizer targeting the ABCC1-induced MDR. Our in vitro and ex vivo data might provide a valuable information for designing the novel effective scheme applicable in the clinical pharmacotherapy of BRAF-mutated/ABCC1-expressing tumors. |
| Klíčová slova oddělená středníkem |
cytochrome P450;non-small cell lung cancer;ABC transporter;multidrug resistance;encorafenib |
| Stránka www, na které se nachází výsledek |
https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=WnhWsZ1eNv |
| DOI výsledku |
10.3390/pharmaceutics14122595 |
| Odkaz na údaje z výzkumu |
- |