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乳腺癌耐药蛋白(BCRP/ABCG2):其在多药耐药中的作用及其基因表达的调控

Breast cancer resistance protein (BCRP/ABCG2): its role in multidrug resistance and regulation of its gene expression.

作者信息

Nakanishi Takeo, Ross Douglas D

机构信息

Department of Membrane Transport and Biopharmaceutics, Kanazawa University School of Pharmaceutical Sciences, Kanazawa, Japan.

出版信息

Chin J Cancer. 2012 Feb;31(2):73-99. doi: 10.5732/cjc.011.10320. Epub 2011 Nov 18.

Abstract

Breast cancer resistance protein (BCRP)/ATP-binding cassette subfamily G member 2 (ABCG2) is an ATP-binding cassette (ABC) transporter identified as a molecular cause of multidrug resistance (MDR) in diverse cancer cells. BCRP physiologically functions as a part of a self-defense mechanism for the organism; it enhances elimination of toxic xenobiotic substances and harmful agents in the gut and biliary tract, as well as through the blood-brain, placental, and possibly blood-testis barriers. BCRP recognizes and transports numerous anticancer drugs including conventional chemotherapeutic and targeted small therapeutic molecules relatively new in clinical use. Thus, BCRP expression in cancer cells directly causes MDR by active efflux of anticancer drugs. Because BCRP is also known to be a stem cell marker, its expression in cancer cells could be a manifestation of metabolic and signaling pathways that confer multiple mechanisms of drug resistance, self-renewal (stemness), and invasiveness (aggressiveness), and thereby impart a poor prognosis. Therefore, blocking BCRP-mediated active efflux may provide a therapeutic benefit for cancers. Delineating the precise molecular mechanisms for BCRP gene expression may lead to identification of a novel molecular target to modulate BCRP-mediated MDR. Current evidence suggests that BCRP gene transcription is regulated by a number of trans-acting elements including hypoxia inducible factor 1α, estrogen receptor, and peroxisome proliferator-activated receptor. Furthermore, alternative promoter usage, demethylation of the BCRP promoter, and histone modification are likely associated with drug-induced BCRP overexpression in cancer cells. Finally, PI3K/AKT signaling may play a critical role in modulating BCRP function under a variety of conditions. These biological events seem involved in a complicated manner. Untangling the events would be an essential first step to developing a method to modulate BCRP function to aid patients with cancer. This review will present a synopsis of the impact of BCRP-mediated MDR in cancer cells, and the molecular mechanisms of acquired MDR currently postulated in a variety of human cancers.

摘要

乳腺癌耐药蛋白(BCRP)/ATP结合盒亚家族G成员2(ABCG2)是一种ATP结合盒(ABC)转运蛋白,被确定为多种癌细胞中多药耐药(MDR)的分子原因。BCRP在生理上作为机体自我防御机制的一部分发挥作用;它增强了肠道和胆道中以及通过血脑屏障、胎盘屏障以及可能的血睾屏障对有毒异源生物物质和有害物质的清除。BCRP识别并转运多种抗癌药物,包括传统化疗药物和临床使用中相对较新的靶向小分子治疗药物。因此,癌细胞中BCRP的表达通过抗癌药物的主动外排直接导致MDR。由于BCRP也被认为是一种干细胞标志物,其在癌细胞中的表达可能是代谢和信号通路的一种表现,这些通路赋予了多种耐药机制、自我更新(干性)和侵袭性(攻击性),从而导致预后不良。因此,阻断BCRP介导的主动外排可能为癌症提供治疗益处。阐明BCRP基因表达的确切分子机制可能会导致识别出一种调节BCRP介导的MDR的新型分子靶点。目前的证据表明,BCRP基因转录受多种反式作用元件调控,包括缺氧诱导因子1α、雌激素受体和过氧化物酶体增殖物激活受体。此外,BCRP启动子的可变使用、去甲基化以及组蛋白修饰可能与癌细胞中药物诱导的BCRP过表达有关。最后,PI3K/AKT信号通路可能在多种条件下调节BCRP功能中起关键作用。这些生物学事件似乎以复杂的方式相互关联。理清这些事件将是开发一种调节BCRP功能以帮助癌症患者的方法的重要第一步。本综述将概述BCRP介导的MDR对癌细胞的影响,以及目前在多种人类癌症中推测的获得性MDR的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ab4/3777471/c6d0ee266414/cjc-31-02-073-g001.jpg

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