ABCG2抑制剂:它们会发现临床相关性吗?

Jerec Ricci, Debbie Lovato, R. Larson
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引用次数: 11

摘要

多重耐药(MDR)是癌症对各种化疗药物产生耐药性的重要途径,一直是癌症患者治疗的障碍。一些ATP结合盒(ABC)转运蛋白已被描述为构成MDR背后的主要机制:ABCB1, ABCC1和ABCG2。在这三者中,ABCG2的独特之处在于它似乎主要在实体肿瘤中表达。尽管最近发现了许多抑制其活性的化合物,但就其对耐多药的贡献而言,它仍然是动物模型和人类中研究最少的转运蛋白之一。虽然阻断ABCG2外排蛋白在逆转癌症耐多药方面具有很大的潜力,但在临床中是否足以克服化疗耐药?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ABCG2 Inhibitors: Will They Find Clinical Relevance?
Multiple drug resistance (MDR) is a prominent way by which cancer develops resistance to various chemotherapeutic agents and continues to be a hurdle in treating cancer patients. A few ATP binding cassette (ABC) transporters have been described as comprising the main mechanism behind MDR: ABCB1, ABCC1, and ABCG2. Of these three, ABCG2 is unique in that it seems to be mainly expressed in solid tumors. Despite the recent discovery of many compounds that inhibit its activity, it remains one of the least well-studied transporters in both animal models and in humans with regard to its contribution to MDR. Though the blockade of the ABCG2 efflux protein has great potential in reversing MDR in cancer, will it be enough to overcome chemoresistance in the clinic?
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