Objective: To investigate the Reversal Effect of Irisquinone (ANKA) on Cisplatin-resistant Human Lung Adenocarcinoma Cell Line (A 549 DDP ) and the change of MRP expression. Methods: MTT assay, flow cytometry, glutath...Objective: To investigate the Reversal Effect of Irisquinone (ANKA) on Cisplatin-resistant Human Lung Adenocarcinoma Cell Line (A 549 DDP ) and the change of MRP expression. Methods: MTT assay, flow cytometry, glutathione reductase recycling assay, RT-PCR were used. Results: None or low cytotoxic concentration of ANKA (10, 20, 30 μmol/L) could increase the sensitivity of A 549 DDP cells to CDDP by 8.2, 7.9 and 8.9-fold in a dose independent manner. After A 549 DDP cells was pretreated with 10 μmol/L ANKA for 12 h, CDDP cytotoxicity was increased 9.41-fold. The GSH content of the cells treated by ANKA is reduced significantly (P<0.001). The GSTπ protein expression was reduced by ANKA depended on its doses. ANKA also reduced expression of MRP protein, dependent on its dose and treating time (P<0.001). MRP mRNA expression was reduced only by 30μmol/L ANKA (P<0.05). Conclusion: The reversal effect of ANKA on A 549 DDP cell was relative to intracellular glutathione system.展开更多
基金the grant from the National 9th five-year program for Scientific Research of China (96-906-01-23).
文摘Objective: To investigate the Reversal Effect of Irisquinone (ANKA) on Cisplatin-resistant Human Lung Adenocarcinoma Cell Line (A 549 DDP ) and the change of MRP expression. Methods: MTT assay, flow cytometry, glutathione reductase recycling assay, RT-PCR were used. Results: None or low cytotoxic concentration of ANKA (10, 20, 30 μmol/L) could increase the sensitivity of A 549 DDP cells to CDDP by 8.2, 7.9 and 8.9-fold in a dose independent manner. After A 549 DDP cells was pretreated with 10 μmol/L ANKA for 12 h, CDDP cytotoxicity was increased 9.41-fold. The GSH content of the cells treated by ANKA is reduced significantly (P<0.001). The GSTπ protein expression was reduced by ANKA depended on its doses. ANKA also reduced expression of MRP protein, dependent on its dose and treating time (P<0.001). MRP mRNA expression was reduced only by 30μmol/L ANKA (P<0.05). Conclusion: The reversal effect of ANKA on A 549 DDP cell was relative to intracellular glutathione system.
