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Combination of gambogic acid with cisplatin enhances the antitumor effects on cisplatin-resistant lung cancer cells by downregulating MRP2 and LRP expression

机译:藤黄酸与顺铂组合通过下调MRP2和LRP表达增强对顺铂耐药性肺癌细胞的抗肿瘤作用

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摘要

Cisplatin resistance is a main clinical problem of lung cancer therapy. Gambogic acid (GA) could prohibit the proliferation of a variety of human cancer cells. However, the effects of GA on cisplatin-resistant lung cancer are still unclear. The objective of the present study was to find out the antitumor effects of GA on cisplatin-resistant human lung cancer A549/DDP cells and further explore its underlying mechanisms. Cell Counting Kit-8 assay was used to observe the impacts of GA and/or cisplatin on the proliferation of lung cancer cells; flow cytometry was used to detect the effects of GA on cell cycle and apoptosis; Western blot was used to examine the effects of GA on the expression of lung resistance protein (LRP) and multidrug resistance-associated protein 2 (MRP2) protein in A549/DDP cells. Our results showed that GA dose- and time-dependently prohibited the proliferation and induced significant cell apoptosis in A549 and A549/DDP cells. GA also induced G0/G1 arrest in both A549/DDP and A549 cells. Moreover, GA upregulated protein expression level of cleaved caspase-3 and Bax and downregulated protein expression level of pro-caspase-9 and Bcl-2 in time- and dose-dependent way in A549/DDP cells. GA combined with cisplatin enhanced the cells apoptotic rate and reduced the cisplatin resistance index in A549/DDP cells. In addition, GA reduced the MRP2 and LRP protein expression level in A549/DDP cells. GA inhibits the proliferation, induces cell cycle arrest and apoptosis in A549/DDP cells. Combination of GA with cisplatin enhances the antitumor effects on cisplatin-resistant lung cancer cells by downregulating MRP2 and LRP expression.
机译:顺铂耐药性是肺癌治疗的主要临床问题。藤黄酸(GA)可能会阻止多种人类癌细胞的增殖。但是,GA对顺铂耐药性肺癌的作用仍不清楚。本研究的目的是发现GA对顺铂耐药的人肺癌A549 / DDP细胞的抗肿瘤作用,并进一步探讨其潜在机制。细胞计数试剂盒8法用于观察GA和/或顺铂对肺癌细胞增殖的影响。流式细胞仪检测GA对细胞周期和凋亡的影响。用Western blot检测GA对A549 / DDP细胞肺耐药蛋白(LRP)和多药耐药相关蛋白2(MRP2)蛋白表达的影响。我们的结果表明,GA剂量和时间依赖性地抑制了A549和A549 / DDP细胞的增殖并诱导了明显的细胞凋亡。 GA还诱导了A549 / DDP和A549细胞的G0 / G1阻滞。而且,GA在A549 / DDP细胞中以时间和剂量依赖性的方式上调了裂解的caspase-3和Bax的蛋白表达水平,并下调了caspase-9和Bcl-2的蛋白表达水平。 GA联合顺铂可提高A549 / DDP细胞的凋亡率,降低顺铂耐药指数。此外,GA降低了A549 / DDP细胞中MRP2和LRP蛋白的表达水平。 GA抑制A549 / DDP细胞的增殖,诱导细胞周期停滞和凋亡。 GA与顺铂的组合通过下调MRP2和LRP表达来增强对顺铂耐药性肺癌细胞的抗肿瘤作用。

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