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首页> 外文期刊>Asian Pacific Journal of Cancer Prevention >Phorbol Ester TPA Modulates Chemoresistance in the Drug Sensitive Breast Cancer Cell Line MCF-7 by Inducing Expression of Drug Efflux Transporter ABCG2
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Phorbol Ester TPA Modulates Chemoresistance in the Drug Sensitive Breast Cancer Cell Line MCF-7 by Inducing Expression of Drug Efflux Transporter ABCG2

机译:Phorbol酯TPA通过诱导药物流出转运蛋白ABCG2的表达调节药物敏感乳腺癌细胞系MCF-7中的化学抑制剂

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Recent studies have indicated a link between levels of cyclooxygenase-2 (COX-2) and development of the multidrug resistance (MDR) phenotype. The ATP-binding cassette sub-family G member 2 (ABCG2) is a major MDR-related transporter protein that is frequently overexpressed in cancer patients. In this study, we aimed to evaluate any positive correlation between COX-2 and ABCG2 gene expression using the COX-2 inducer 12-O-tetradecanoylphorbol-13-acetate (TPA) in human breast cancer cell lines. ABCG2 mRNA and protein expression was studied using real-time RT-PCR and flow cytometry, respectively. A significant increase of COX-2 mRNA expression (up to 11-fold by 4 h) was induced by TPA in MDA-MB-231 cells, this induction effect being lower in MCF-7 cells. TPA caused a considerable increase up to 9-fold in ABCG2 mRNA expression in parental MCF-7 cells, while it caused a small enhancement in ABCG2 expression up to 67 % by 4 h followed by a time-dependent decrease in ABCG2 mRNA expression in MDA-MB-231 cells. TPA treatment resulted in a slight increase of ABCG2 protein expression in MCF-7 cells, while a time-dependent decrease in ABCG2 protein expression was occurred in MDA-MB-231 cells. In conclusion, based on the observed effects of TPA in MDA-Mb-231 cells, it is proposed that TPA up-regulates ABCG2 expression in the drug sensitive MCF-7 breast cancer cell line through COX-2 unrelated pathways.
机译:最近的研究表明了环氧氧酶-2(COX-2)水平与多药耐药性(MDR)表型的开发之间的联系。 ATP结合盒亚族Gement 2(ABCG2)是癌症患者经常过表达的主要MDR相关转运蛋白。在本研究中,我们旨在使用人乳腺癌细胞系中的COX-2诱导型12-O-四癸酰基(TPA)评估COX-2和ABCG2基因表达的任何正相关。使用实时RT-PCR和流式细胞术研究ABCG2 mRNA和蛋白质表达。 TPA在MDA-MB-231细胞中,TPA诱导Cox-2 mRNA表达(高达11倍)的显着增加,在MCF-7细胞中,该诱导效果降低。 TPA在亲本MCF-7细胞中,在ABCG2 mRNA表达中引起相当大的增加高达9倍,而ABCG2表达中的少量增强高达67%〜4小时,然后在MDA中的ABCG2 mRNA表达中的时间依赖性降低-MB-231细胞。 TPA处理导致MCF-7细胞中ABCG2蛋白表达的略微增加,而在MDA-MB-231细胞中发生ABCG2蛋白表达的时间依赖性降低。总之,基于TPA在MDA-MB-231细胞中的观察到的影响,提出TPA通过COX-2无关途径调节药物敏感MCF-7乳腺癌细胞系中的ABCG2表达。

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