MIF和GSTpi在激素依赖型前列腺癌耐药产生中的调控作用

D-S Yu, J C Lin, D S Hsieh, S Y Chang, C F Lee
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引用次数: 6

摘要

MIF和GSTpi在多药耐药型前列腺癌细胞中表达上调。本研究旨在探讨这些基因与多药耐药(mdr-1)基因在前列腺癌获得性多药耐药中的关系。采用流式细胞术和western blotting检测MIF、GSTpi和gp-170在多药耐药(MDR)亚耐药细胞和天然耐药细胞中的表达。采用RT-PCR法分析各基因mRNA表达水平。采用MTT法测定肿瘤细胞和稳定转染物对紫杉醇的化学敏感性。MDR前列腺癌亚群中MIF、GSTpi和gp-170蛋白水平较亲本细胞升高。在western blotting分析中,MIF和GSTpi稳定转染细胞表达的MIF和GSTpi蛋白水平分别高于亲本细胞。RT-PCR和流式细胞术分析结果表明,MIF和GSTpi稳定转染与载体对照相比,mdr-1基因的表达和pg-170的产生均有所增加。MTT结果表明,MIF或GSTpi的化学抗性增加与gp-170蛋白产量增加有关。激素非依赖型前列腺癌获得性耐药过程中MIF和GSTpi的上调可能同时部分调节gp-170的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of MDR-1 gene by MIF and GSTpi with drug resistance generation in hormone independent prostate cancer.

The expression of MIF and GSTpi were upregulated in prostate cancer cells with mulitdrug resistant phenotype. The aim of this study is to determine the relationship between these genes and multidrug resistance (mdr-1) gene in acquired multidrug resistance of prostate cancer. The expression of MIF, GSTpi and gp-170 in multidrug resistant (MDR) subline or native cells were determined using flow cytometry and western blotting. The mRNA level of various genes was analyzed with RT-PCR method. The chemosensitivity of tumor cells and stable transfectants to paclitaxel was measured using MTT (tetrazolium bromide) assay. The protein levels of MIF, GSTpi and gp-170 increased in MDR sublines of prostate cancer when compared with their parental cells. The MIF and GSTpi stable transfectants expressed higher MIF and GSTpi protein levels than their parental cells in western blotting analysis, respectively. The expression of mdr-1 gene and the production of pg-170 were also increased in either MIF or GSTpi stable transfectants when compared with vector control by using RT-PCR and flow cytometric analysis. The MTT results demonstrated that the increased chemoresistance was correlated with the increased production of gp-170 protein in either MIF or GSTpi transfectants. The upregulation of MIF and GSTpi during the development of acquired drug resistance of hormone independent prostate cancer may simultaneously and partially modulate the activation of gp-170.

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