Off-target identification by chemical proteomics for the understanding of drug side effects

Off-target identification by chemical proteomics for the understanding of drug side effects
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通过化学蛋白质组学进行脱靶识别以了解药物副作用

DOI:
10.1080/14789450.2020.1873134
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发表时间:
2020-10
影响因子:
3.4
通讯作者:
Wang Kui
Wang Kui
中科院分区:
生物学3区
文献类型:
--
作者:
Song Yabing;Luo Li;Wang Kui

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药物副作用(也称为不良事件)是在人类正常使用剂量下发生的药物的有害和意外反应[1]。研究表明,多达 11% 的入院率、20% 的临床试验失败、几种备受瞩目的药物撤回(如 Vioxx、Lipobay 和 Thalomid)以及大部分治疗不依从事件都是由药物副作用造成的 [2]。揭示副作用机制无疑将促进未来临床应用中规避药物副作用的干预策略的制定。在过去的几十年里,化学蛋白质组学方法和质谱(MS)技术的快速发展使得药物脱靶的无偏反卷积成为可能,极大地促进了我们对副作用机制的理解。
Drug side effects (also known as adverse events) are noxious and unintended responses of drugs that occur at doses normally used in humans [1]. It has been shown that drug side effects should be responsible for as much as 11% of hospital admissions, 20% of clinical trial failures, several high-profile drug withdrawals (such as Vioxx, Lipobay, and Thalomid), and a large portion of therapeutic noncompliance incidents [2]. Unraveling the side effect mechanisms will undoubtedly promotes the development of intervention strategies to circumvent drug side effects in future clinical application. During the past decades, the rapid development of chemical proteomics approaches and mass spectrometry (MS) technologies has enabled the unbiased deconvolution of drug off-targets, contributing greatly to our understanding of the side effect mechanisms.
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