Zarei S, Reza J Zavar, Jaliani H Zarei, Hajizadeh M R, Sargazi S, Hosseinian H
Bratisl Lek Listy. 2019;120(6):468-475. doi: 10.4149/BLL_2019_075.
Previous studies on the efficacy of platinum-based drugs and selective inhibitors of proteasome have revealed promising outcomes. This study is aimed to evaluate the effects of the combination of cisplatin and carfilzomib on the cell death induction and drug efflux transporters expression in cisplatin-sensitive (A2780s) and cisplatin-resistant (A2780cp) ovarian cancer cells lines.
MTT cytotoxic assay was conducted to determine the cytotoxicity. Drug interactions were analyzed based on Chou-Talalay's principles and real-time PCR analysis was performed to determine possible alterations in mRNA levels of MRP1 and BCRP.
A2780s cells were more susceptible to both cisplatin and carfilzomib while analyses of drug interactions between the two agents showed synergistic effects in all affected fractions of drug-treated A2780s and A2780cp cells (CI<0.9) with the combination indices being significantly lower in A2780cp cells (p < 0.01). We also found that although mRNA levels of BCRP and MRP1 were significantly altered in both cells exposed to each drug alone, only the combination regimen was able to significantly reduce the mRNA levels of these genes in A2780cp cells (p<0.001).
This combination might be a potential strategy for suppressing cell growth via downregulating the drug efflux transporters expression, especially in cisplatin-resistant ovarian cancer cells (Fig. 3, Ref. 45).
先前关于铂类药物和蛋白酶体选择性抑制剂疗效的研究已显示出有前景的结果。本研究旨在评估顺铂与卡非佐米联合使用对顺铂敏感(A2780s)和顺铂耐药(A2780cp)卵巢癌细胞系中细胞死亡诱导及药物外排转运蛋白表达的影响。
采用MTT细胞毒性试验来确定细胞毒性。基于Chou-Talalay原理分析药物相互作用,并进行实时PCR分析以确定MRP1和BCRP的mRNA水平可能发生的变化。
A2780s细胞对顺铂和卡非佐米均更敏感,而对这两种药物之间的相互作用分析显示,在药物处理的A2780s和A2780cp细胞的所有受影响部分中均有协同作用(CI<0.9),且联合指数在A2780cp细胞中显著更低(p<0.01)。我们还发现,尽管单独暴露于每种药物的两种细胞中BCRP和MRP1的mRNA水平均有显著改变,但只有联合用药方案能够显著降低A2780cp细胞中这些基因的mRNA水平(p<0.001)。
这种联合使用可能是一种通过下调药物外排转运蛋白表达来抑制细胞生长的潜在策略,尤其是在顺铂耐药的卵巢癌细胞中(图3,参考文献45)。