首页> 外文期刊>International Journal of Molecular Sciences >Modulation of MDR1 and MRP3 Gene Expression in Lung Cancer Cells after Paclitaxel and Carboplatin Exposure
【24h】

Modulation of MDR1 and MRP3 Gene Expression in Lung Cancer Cells after Paclitaxel and Carboplatin Exposure

机译:紫杉醇和卡铂暴露后肺癌细胞中MDR1和MRP3基因表达的调控

获取原文
           

摘要

Carboplatin-paclitaxel is a reference regimen in the treatment of locally advanced or disseminated non-small cell lung cancer (NSCLC). This paper discusses the multidrug resistance developed with this drug combination, which is one of the major obstacles to successful treatment. In order to understand and overcome the drug resistance pattern of NSCLC after carboplatin plus paclitaxel exposure, levels of mRNA expression of multidrug resistance 1 (MDR1) and multidrug resistance-associated protein 3 (MRP3) were investigated in primary NSCLC cell lines (A-549 and A-427) and a metastasis-derived NSCLC cell line (NODO). Our results showed that exposure of the three NSCLC lines to plasma concentrations of paclitaxel (5 μM) produced an increase in MDR1 expression, while MRP3 showed no alteration in expression. By contrast, the same cells exposed to carboplatin plasma concentrations (30 μM) showed overexpression of MRP3. In these cells, MDR1 showed no expression changes. Interestingly, the combination of both paclitaxel and carboplatin caused increased expression of the MDR1 drug resistance gene rather than the individual treatments. These results suggest that carboplatin and paclitaxel may induce drug resistance mediated by MDR1 and MRP3, which may be enhanced by the simultaneous use of both drugs.
机译:卡铂-紫杉醇是治疗局部晚期或弥漫性非小细胞肺癌(NSCLC)的参考方案。本文讨论了这种药物联合开发产生的多药耐药性,这是成功治疗的主要障碍之一。为了了解和克服卡铂+紫杉醇暴露后NSCLC的耐药模式,在原发性NSCLC细胞系(A-549)中研究了多药耐药1(MDR1)和多药耐药相关蛋白3(MRP3)的mRNA表达水平。和A-427)和转移衍生的NSCLC细胞系(NODO)。我们的结果表明,将三种NSCLC系暴露于紫杉醇(5μM)的血浆浓度会使MDR1表达增加,而MRP3则没有表达改变。相反,暴露于卡铂血浆浓度(30μM)的相同细胞显示MRP3过表达。在这些细胞中,MDR1没有表达变化。有趣的是,紫杉醇和卡铂的组合导致MDR1耐药基因的表达增加,而不是单独的治疗。这些结果表明卡铂和紫杉醇可诱导由MDR1和MRP3介导的耐药性,同时使用两种药物均可增强耐药性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号