首页> 外文会议>BioMedical Information Engineering, 2009. FBIE 2009 >Relationship between methylation status of multi-drug resistance protein (MRP) and multi-drug resistance in lung cancer cell lines
【24h】

Relationship between methylation status of multi-drug resistance protein (MRP) and multi-drug resistance in lung cancer cell lines

机译:肺癌细胞多药耐药蛋白(MRP)甲基化状态与多药耐药的关系

获取原文

摘要

Objective: To study the relationship between the methylation status of multi-drug resistance protein (MRP) gene and the expression of its mRNA and protein in lung cancer cell lines. Methods: Human lung cell line WI-38.1ung adenocarcinoma cell line SPCA-1 and its drug-resistant cells induced by different concentrations of doxorubicin were treated with restriction endonuclease Eco47III. The methylation status of MRP was examined by PCR,and the expressions of its mRNA and protein were evaluated by in situ hybridization and immunohistochemistry. Resuits: MRP gene promoter region of WI-38 cells was in hypermethylation status.but the promoter region of MRP in SPCA-1 cells and their resistant derivatives induced by different concentrations of doxorubicin were in hypomethylation status.There were Significant differences in the expression of MRP mRNA among WI-38 cell line. SPCA-1 cells and their drug-resistan t derivatives induced by different concentration of doxorubicin. Consistently. MRP immunostaining presented similar significant differences. Conclusion: The promoter region of MRP in SPCA-1 lung adenocarcinoma cells was in hypomethylation status. The hypomethylation status of regulatory region of MRP promoter is an important structural basis that can increase the activity of transcription and results in the development of drug resistance in lung cancer.
机译:目的:探讨肺癌细胞多药耐药蛋白(MRP)基因甲基化状态与其mRNA和蛋白表达的关系。方法:用限制性核酸内切酶Eco47III处理人肺细胞株WI-38.1ung腺癌细胞系SPCA-1及其对不同浓度阿霉素诱导的耐药细胞。通过PCR检测MRP的甲基化状态,并通过原位杂交和免疫组化检测其mRNA和蛋白的表达。结果:WI-38细胞的MRP基因启动子区域处于高甲基化状态,但不同浓度的阿霉素诱导的SPCA-1细胞中MRP的启动子区域及其耐药衍生物处于低甲基化状态。 WI-38细胞系中的MRP mRNA。不同浓度的阿霉素诱导SPCA-1细胞及其耐药性衍生物。始终如一。 MRP免疫染色表现出相似的显着差异。结论:SPCA-1肺腺癌细胞中MRP的启动子区域处于低甲基化状态。 MRP启动子调控区的低甲基化状态是重要的结构基础,可以增加转录活性并导致肺癌耐药性的发展。

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