Regulation of Mdr1, MRP1 gene and their protein products P-glycoprotein, multid rug resistance associated protein 1 in leukemic cells by Quercetin
Jie-Ying Han
Abstract
Jie-Ying Han
Abstract
Objective To investigate the regulation of membrane transporters in leukemic cells by quer cetin.Methods MTT cell viability assay was adopted for verifying the chemosensitization of Q u ercetin to Daunorubicin (DNR) in K562/ADM and HL-60/ADM cells and the reverse c oncentration was determined, then the expression of Mdr1, MRP1 gene and their pr o tein products P-glycoprotein (P-gp) and multidrug resistance associated protei n 1 (MRP1) were analysed by RT-PCR and flow cytometry using monoclonal antibody before and after exposure to Quercetin. Results Comparing with K562/S, 20~40 μmol/L Quercetin in vitro could remarkably inc rease the sensitivity of K562/ADM to DNR and down-regulate the expression of Md r1, MRP1 gene and their protein products P-gp and MRP1, so as to reverse the multi drug resistance. Conclusion Quercetin may become a candidate of effective multi-drug resistance-rev ersing agent with low toxicity for leukemia chemotherapy.
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Objective To investigate the regulation of membrane transporters in leukemic cells by quer cetin.Methods MTT cell viability assay was adopted for verifying the chemosensitization of Q u ercetin to Daunorubicin (DNR) in K562/ADM and HL-60/ADM cells and the reverse c oncentration was determined, then the expression of Mdr1, MRP1 gene and their pr o tein products P-glycoprotein (P-gp) and multidrug resistance associated protei n 1 (MRP1) were analysed by RT-PCR and flow cytometry using monoclonal antibody before and after exposure to Quercetin. Results Comparing with K562/S, 20~40 μmol/L Quercetin in vitro could remarkably inc rease the sensitivity of K562/ADM to DNR and down-regulate the expression of Md r1, MRP1 gene and their protein products P-gp and MRP1, so as to reverse the multi drug resistance. Conclusion Quercetin may become a candidate of effective multi-drug resistance-rev ersing agent with low toxicity for leukemia chemotherapy.
Key concepts: Daunorubicin, P-glycoprotein, Pharmacology, Flow cytometry, Multiple drug resistance, K562 cells, Viability assay, Molecular biology