Phenolic compounds that modulate Multi Drug Resistance through inhibiting of P-glycoprotein encoded by gene ABCB1

Önder Yumrutaş, Pınar Yumrutaş
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Abstract

One of the most important challenges in the fight against cancer is acquired drug resistance. P-glycoprotein (P-gp), encoded by the ABCB1 gene in many organs, is one of the important factors involved in the development of drug resistance. P-gp is mainly involved in efflux of toxic substances such as xenobiotics from the cell. In addition to these, it also plays a role the efflux of drugs used in the treatment of cancer, the rate of success in cancer treatment reduces. Phenolic compounds are chemicals that are naturally synthesized in plants and have many biological activities, especially antioxidant and anticancer. In previous studies, it was determined that in addition to their anticancer activities, phenolics modulate the acquired drug resistance by inhibiting the expression and function of P-gp. In this review, phenolic compounds that play a role in breaking multi-drug resistance by inhibiting the activation and expression of P-gp are discussed.
通过抑制ABCB1基因编码的p糖蛋白调控多重耐药的酚类化合物
在与癌症的斗争中,最重要的挑战之一是获得性耐药性。p -糖蛋白(P-gp)是多种器官中由ABCB1基因编码的一种重要的耐药因子。P-gp主要参与有毒物质如外源物质从细胞外排。除了这些,它还起到了药物外排的作用,用于治疗癌症,降低了癌症治疗的成功率。酚类化合物是植物中自然合成的化学物质,具有多种生物活性,尤其是抗氧化和抗癌活性。在以往的研究中发现,除了具有抗癌活性外,酚类物质还通过抑制P-gp的表达和功能来调节获得性耐药。本文综述了酚类化合物通过抑制P-gp的激活和表达来打破多药耐药的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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