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Talazoparib nanoparticles for overcoming multidrug resistance in triple‐negative breast cancer
Author(s) -
Guney Eskiler Gamze,
Cecener Gulsah,
Egeli Unal,
Tunca Berrin
Publication year - 2020
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.29552
Subject(s) - abcg2 , efflux , calcein , triple negative breast cancer , breast cancer , multiple drug resistance , cancer research , western blot , drug resistance , chemistry , pharmacology , biology , cancer , medicine , atp binding cassette transporter , gene , biochemistry , transporter , microbiology and biotechnology , membrane
Herein, we investigated efflux pumps‐mediated talazoparib‐resistance in the treatment of triple‐negative breast cancer (TNBC). Furthermore, we produced a novel talazoparib‐solid lipid nanoparticles (SLNs) and then explored in vitro therapeutic efficacy of talazoparib‐SLNs to overcome talazoparib‐resistance in TNBC cells. Talazoparib‐SLNs formulation was produced and then characterized. Calcein and Rho‐123 were used to analyze the functional activity of drug efflux pumps in these cells. Additionally, RT‐PCR, western blot and immunofluorescence analysis were used to detect the messenger RNA, and protein expression level, and cellular localization of the multidrug resistance (MDR1), breast cancer resistance protein (BCRP), and MRP1. We found that talazoparib efflux was mediated by BCRP and MRP1 pumps in TNBC cells. Talazoparib‐SLNs could significantly enhance therapeutic efficacy of talazoparib. Furthermore, talazoparib‐SLNs were more effective in the suppression of MDR1, BCRP , and MRP1 gene and protein expression levels than talazoparib. Consequently, this study suggests that talazoparib‐SLNs formulation represents a promising therapeutic carrier to reverse MDR‐mediated resistance in TNBC.