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通过抑制ABCB1逆转癌症多药耐药性:最新进展

Cancer multidrug-resistance reversal by ABCB1 inhibition: A recent update.

作者信息

Engle Kritika, Kumar Gautam

机构信息

Department of Natural Products, Chemical Sciences, National Institute of Pharmaceutical Education and Research-Hyderabad, Hyderabad, Balanagar, 500037, India.

Department of Natural Products, Chemical Sciences, National Institute of Pharmaceutical Education and Research-Hyderabad, Hyderabad, Balanagar, 500037, India.

出版信息

Eur J Med Chem. 2022 Sep 5;239:114542. doi: 10.1016/j.ejmech.2022.114542. Epub 2022 Jun 17.

DOI:10.1016/j.ejmech.2022.114542
PMID:35751979
Abstract

Chemotherapy is one of the most common treatments for cancer that uses one or more anti-cancer drugs as a part of the standardized chemotherapy regimen. Cytotoxic chemicals delay and prevent cancer cells from multiplying, invading, and metastasizing. However, the significant drawbacks of cancer chemotherapy are the lack of selectivity of the cytotoxic drugs to tumour cells and normal cells and the development of resistance by cells for the particular drug or the combination of drugs. Multidrug resistance (MDR) is the low sensitivity of specific cells against drugs associated with cancer chemotherapy. The most common mechanisms of anticancer drug resistance are: (a) drug-dependent MDR (b) target-dependent MDR, and (c) drug target-independent MDR. In all the factors, the overexpression of multidrug efflux systems contributes significantly to the increased resistance in the cancer cells. Multidrug resistance due to efflux of anticancer drugs by membrane ABC transporters includes ABCB1, ABCC1, and ABCG2. ABCB1 inhibition can restore the sensitivity of the cancerous cells toward chemotherapeutic drugs. In this review, we discussed ABCB1 inhibitors under clinical studies with their mode of action, potency and selectivity. Also, we have highlighted the contribution of repurposing drugs, biologics and nano formulation strategies to combat multidrug resistance by modulating the ABCB1 activity.

摘要

化疗是癌症最常见的治疗方法之一,它使用一种或多种抗癌药物作为标准化化疗方案的一部分。细胞毒性化学物质可延迟并阻止癌细胞增殖、侵袭和转移。然而,癌症化疗的显著缺点是细胞毒性药物对肿瘤细胞和正常细胞缺乏选择性,以及细胞对特定药物或药物组合产生耐药性。多药耐药性(MDR)是特定细胞对与癌症化疗相关药物的低敏感性。抗癌药物耐药性的最常见机制是:(a)药物依赖性MDR(b)靶点依赖性MDR,以及(c)药物靶点非依赖性MDR。在所有这些因素中,多药外排系统的过表达显著导致癌细胞耐药性增加。由膜ABC转运蛋白对抗癌药物进行外排引起的多药耐药性包括ABCB1、ABCC1和ABCG2。ABCB1抑制可恢复癌细胞对化疗药物的敏感性。在本综述中,我们讨论了处于临床研究阶段的ABCB1抑制剂及其作用方式、效力和选择性。此外,我们强调了通过重新利用药物、生物制剂和纳米制剂策略来调节ABCB1活性以对抗多药耐药性的作用。

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