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研究中的 ABC 转运蛋白抑制剂。

Investigational ABC transporter inhibitors.

机构信息

Queen Mary University of London, Blizard Institute, Barts and The London School of Medicine and Dentistry, Centre for Diabetes, Inositide Signalling Group, 4 Newark Street, London, UK.

出版信息

Expert Opin Investig Drugs. 2012 May;21(5):657-66. doi: 10.1517/13543784.2012.679339.

Abstract

INTRODUCTION

Multidrug resistance (MDR) is the main cause of failure in cancer therapy. One mechanism responsible for MDR is the active efflux of drugs by ATP-binding cassette (ABC) transporters. Several agents have been developed to block transporter-mediated drug efflux and some of these compounds have entered Phase II/III clinical testing. Evidence is also emerging of the role played by ABC transporters in cancer cell signalling that is likely to be important in disease progression and which is distinct from MDR.

AREAS COVERED

This article reviews current literature to analyse the rationale for targeting ABC transporters in cancer. Preclinical and clinical results of ABC transporter inhibitors in early clinical trials, as single agents or in combination with other drugs, are described. The development of new strategies to target MDR and the emerging roles of ABC transporters in cancer signalling are discussed.

EXPERT OPINION

The intense active search for safe and effective inhibitors of ABC transporters has led to some success in MDR reversal in preclinical studies. However, there has been little impact on clinical outcome. The discovery of novel, potent and nontoxic inhibitors as well as new treatment strategies is therefore needed.

摘要

简介

多药耐药性(MDR)是癌症治疗失败的主要原因。负责 MDR 的一个机制是通过 ATP 结合盒(ABC)转运蛋白主动排出药物。已经开发了几种药物来阻断转运蛋白介导的药物外排,其中一些化合物已经进入 II/III 期临床试验。越来越多的证据表明 ABC 转运蛋白在癌症细胞信号转导中发挥作用,这可能对疾病进展很重要,并且与 MDR 不同。

涵盖领域

本文综述了当前文献,分析了针对癌症中 ABC 转运蛋白的基本原理。描述了 ABC 转运蛋白抑制剂在早期临床试验中作为单一药物或与其他药物联合使用的临床前和临床结果。讨论了针对 MDR 的新策略的发展以及 ABC 转运蛋白在癌症信号转导中的新兴作用。

专家意见

针对 ABC 转运蛋白的安全有效抑制剂的积极探索,在临床前研究中已成功逆转了一些 MDR。然而,对临床结果的影响很小。因此,需要发现新型、有效且无毒的抑制剂以及新的治疗策略。

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