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利用已有资源:从现有组学数据中挖掘新药再利用策略。

Using What We Already Have: Uncovering New Drug Repurposing Strategies in Existing Omics Data.

机构信息

Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, Tennessee 37203, USA.

Department of Medicine, Division of Infectious Diseases, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2020 Jan 6;60:333-352. doi: 10.1146/annurev-pharmtox-010919-023537. Epub 2019 Jul 23.

Abstract

The promise of drug repurposing is to accelerate the translation of knowledge to treatment of human disease, bypassing common challenges associated with drug development to be more time- and cost-efficient. Repurposing has an increased chance of success due to the previous validation of drug safety and allows for the incorporation of omics. Hypothesis-generating omics processes inform drug repurposing decision-making methods on drug efficacy and toxicity. This review summarizes drug repurposing strategies and methodologies in the context of the following omics fields: genomics, epigenomics, transcriptomics, proteomics, metabolomics, microbiomics, phenomics, pregomics, and personomics. While each omics field has specific strengths and limitations, incorporating omics into the drug repurposing landscape is integral to its success.

摘要

药物重定位的承诺是加速知识转化为人类疾病的治疗,避免与药物开发相关的常见挑战,从而更省时、更高效。由于先前已经验证了药物的安全性,重定位的成功率更高,并且可以纳入组学。产生假说的组学过程为药物重定位决策方法提供关于药物疗效和毒性的信息。本文综述了药物重定位策略和方法,涉及以下组学领域:基因组学、表观基因组学、转录组学、蛋白质组学、代谢组学、微生物组学、表型组学、前基因组学和个体组学。虽然每个组学领域都有其特定的优势和局限性,但将组学纳入药物重定位领域对于其成功至关重要。

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