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姜黄素逆转P-糖蛋白介导的多药耐药机制 被引量:1

Reversal of P-glycoprotein-mediated multidrug resistance mechanism by curcumin
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摘要 多药耐药(MDR)是临床药物抗癌失败的重要原因之一,涉及多种机制。其中,P-糖蛋白(P-gp)介导的经典MDR机制与MDR的形成关系密切,通过“药泵”效应排出细胞内化疗药物,显著降低化疗疗效。姜黄素主要提取自中药姜黄的地下根茎,具有广泛的药理活性。近年研究发现,姜黄素通过调控多种信号通路,抑制P-gp的功能和表达,发挥逆转肿瘤MDR的作用。 Multidrug resistance (MDR) is one of the important reasons for the failure of clinical anti- cancer drugs, involving multiple mechanisms. Among them, the classical MDR mechanism mediated by P-gly- coprotein (P-gp) is closely related to the formation of MDR, which can excrete intracellular chemotherapeutic drugs through the "drug pump" effect and significantly reduce the therapeutic effect. Curcumin is mainly ex- tracted from the underground rhizome of Chinese medicine turmeric, with a wide range of pharmacological activity. Recent studies have found that curcumin also has a role in reversing the MDR of the tumor, by inhibi- ting both P-gp function and expression, and this process involves a variety of signal paths.
出处 《国际肿瘤学杂志》 CAS 2017年第10期758-761,共4页 Journal of International Oncology
基金 湖北省卫生计生委青年人才项目(WJ2017H0036)
关键词 姜黄素 P糖蛋白 多药耐药 信号通路 Curcumin P-glycoprotein Multidrug resistance Signal path
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