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蛇毒精氨酸酯酶Agkihpin对人鼻咽癌CNE-2细胞系MRP1表达的影响[J]. 肿瘤防治研究, 2011, 38(07): 731-735. DOI: 10.3971/j.issn.1000-8578.2011.07.001
引用本文: 蛇毒精氨酸酯酶Agkihpin对人鼻咽癌CNE-2细胞系MRP1表达的影响[J]. 肿瘤防治研究, 2011, 38(07): 731-735. DOI: 10.3971/j.issn.1000-8578.2011.07.001
Effect of Agkihpin-an Arginine Esterase from Venom on Expression of MRP1 in CNE-2 Cells[J]. Cancer Research on Prevention and Treatment, 2011, 38(07): 731-735. DOI: 10.3971/j.issn.1000-8578.2011.07.001
Citation: Effect of Agkihpin-an Arginine Esterase from Venom on Expression of MRP1 in CNE-2 Cells[J]. Cancer Research on Prevention and Treatment, 2011, 38(07): 731-735. DOI: 10.3971/j.issn.1000-8578.2011.07.001

蛇毒精氨酸酯酶Agkihpin对人鼻咽癌CNE-2细胞系MRP1表达的影响

Effect of Agkihpin-an Arginine Esterase from Venom on Expression of MRP1 in CNE-2 Cells

  • 摘要: 目的探讨蛇毒精氨酸酯酶Agkihpin对人鼻咽癌CNE-2细胞系中多药耐药相关蛋白MRP1表达的影响,并试图阐明Agkihpin抑制CNE-2细胞的机制。方法用不同浓度的Agkihpin处理细胞72 h后,应用免疫细胞化学、Western blot、RT-PCR法检测MRP1在CNE-2细胞中的表达。结果不同浓度Agkihpin作用CNE-2细胞72 h后MRP1表达均降低,并呈现出一定的浓度依赖效应,显示Agkihpin可显著下调CNE-2细胞中MRP1表达。各加药组与不加Agkihpin组比较,差异具有统计学意义(P<0.05)。结论在人低分化鼻咽癌CNE-2细胞系中,Agkihpin能抑制MRP1的表达,并且随浓度的增大抑制作用增加,这可能是Agkihpin能降低鼻咽癌细胞活力的原因之一;Agkihpin抑制MRP1的表达提示在一定程度上可提高肿瘤细胞对化疗药物的敏感度。

     

    Abstract: ObjectiveTo explore the effect of Agkihpin on the expression of multidrug resistance associated protein 1(MRP1) in nasopharyngeal carcinoma CNE-2 cell line, and try to describe the mechanism of Agkihpin inhibiting CNE-2. MethodsThe cultured cells were treated with different concentrations of Agkihpin for 72 h. The expression level of MRP1 in CNE-2 cell line was assayed by immunocytochemistry, Western blot and RT-PCR. ResultsComparing with Agkihpin absent group, the MRP1 expression levels in CNE-2 cells were reduced significantly after the treatment of different concentrations of Agkihpin (P<0.05), in a concentration-dependent manner, which shows that Agkihpin could significantly down-regulate the expression of MRP1 in CNE-2 cells. ConclusionAgkihpin can inhibit the expression of MRP1 in CNE-2 cells, which is likely to be one of reasons for Agkihpin inhibiting the cellular vitality of nasopharyngeal carcinoma cell, and be likely to enhance the sensitivity of CNE-2 cells to chemotherapeutic drugs to some extent.

     

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