Department of Pharmaceutical Sciences, College of Pharmacy, Natural and Health Sciences, Manchester University, Fort Wayne, Indiana, United States.
PLoS One. 2022 Aug 30;17(8):e0273582. doi: 10.1371/journal.pone.0273582. eCollection 2022.
The number of adverse drug events in the United States is critically high, with annual rates exceeding 1 million cases over the last nine years. One cause of adverse drug events is the underlying genetic variation that can alter drug responses. Pharmacogenomics is a growing field that seeks to better understand the relationship between a patient's genetics and drug efficacy. Currently, pharmacogenomics relies largely on human trials, as there is not a well-developed animal model for studying preventative measures and alternative treatments. Here, we analyzed pharmacogene expression at two developmental time points in zebrafish to demonstrate the potential of using this model organism for high-throughput pharmacogenomics research. We found that 76% of tiered human pharmacogenes have a zebrafish ortholog, and of these, many have highly conserved amino acid sequences. Additional gene ontology analysis was used to classify pharmacogenes and identify candidate pathways for future modeling in zebrafish. As precision medicine burgeons, adopting a high-throughput in vivo model such as the zebrafish could greatly increase our understanding of the molecular pathology underlying adverse drug events.
美国的药物不良反应数量极高,在过去九年中,每年的发生率超过 100 万例。药物不良反应的一个原因是潜在的基因变异,它可以改变药物的反应。药物基因组学是一个正在发展的领域,旨在更好地理解患者的遗传和药物疗效之间的关系。目前,药物基因组学在很大程度上依赖于人体试验,因为目前还没有一个完善的动物模型来研究预防措施和替代疗法。在这里,我们分析了斑马鱼在两个发育时间点的药物基因表达,以证明使用这种模式生物进行高通量药物基因组学研究的潜力。我们发现,分层的人类药物基因中有 76%有斑马鱼的直系同源物,其中许多具有高度保守的氨基酸序列。还进行了额外的基因本体分析,以对药物基因进行分类,并确定未来在斑马鱼中建模的候选途径。随着精准医学的兴起,采用高通量的体内模型,如斑马鱼,可以大大提高我们对药物不良反应潜在分子病理学的理解。