Center for Applied Genomics & Precision Medicine, Duke University School of Medicine, Durham, NC, United States.
Division of Hematology, Department of Medicine, Duke University Medical Center, Durham, NC, United States.
Br J Clin Pharmacol. 2022 May;88(5):2074-2083. doi: 10.1111/bcp.15127. Epub 2021 Nov 27.
Aspirin has known effects beyond inhibiting platelet cyclooxygenase-1 (COX-1) that have been incompletely characterized. Transcriptomics can comprehensively characterize the on- and off-target effects of medications. We used a systems pharmacogenomics approach of aspirin exposure in volunteers coupled with serial platelet function and purified platelet mRNA sequencing to test the hypothesis that aspirin's effects on the platelet transcriptome are associated with platelet function. We prospectively recruited 74 adult volunteers for a randomized crossover study of 81- vs. 325 mg/day, each for 4 weeks. Using mRNA sequencing of purified platelets collected before and after each 4-week exposure, we identified 208 aspirin-responsive genes with no evidence for dosage effects. In independent cohorts of healthy volunteers and patients with diabetes, we validated aspirin's effects on five genes: EIF2S3, CHRNB1, EPAS1, SLC9A3R2 and HLA-DRA. Functional characterization of the effects of aspirin on mRNA as well as platelet ribosomal RNA demonstrated that aspirin may act as an inhibitor of protein synthesis. Database searches for small molecules that mimicked the effects of aspirin on platelet gene expression in vitro identified aspirin but no other molecules that share aspirin's known mechanisms of action. The effects of aspirin on platelet mRNA were correlated with higher levels of platelet function both at baseline and after aspirin exposure-an effect that counteracts aspirin's known antiplatelet effect. In summary, this work collectively demonstrates a dose-independent effect of aspirin on the platelet transcriptome that counteracts the well-known antiplatelet effects of aspirin.
阿司匹林除了抑制血小板环氧化酶-1(COX-1)外,还有其他尚未完全阐明的作用。转录组学可以全面描述药物的靶内和靶外作用。我们采用志愿者阿司匹林暴露的系统药物基因组学方法,结合血小板功能的连续检测和纯化血小板 mRNA 测序,来验证阿司匹林对血小板转录组的作用是否与血小板功能相关的假设。我们前瞻性地招募了 74 名成年志愿者,进行了一项 81mg/天和 325mg/天的随机交叉研究,每个剂量组各持续 4 周。在每个 4 周暴露前后收集的纯化血小板中进行 mRNA 测序,我们鉴定了 208 个阿司匹林反应基因,没有证据表明存在剂量效应。在健康志愿者和糖尿病患者的独立队列中,我们验证了阿司匹林对五个基因的作用:EIF2S3、CHRNB1、EPAS1、SLC9A3R2 和 HLA-DRA。阿司匹林对 mRNA 以及血小板核糖体 RNA 的作用的功能特征表明,阿司匹林可能作为蛋白质合成抑制剂。在体外模拟阿司匹林对血小板基因表达作用的小分子数据库搜索发现,阿司匹林但没有其他与阿司匹林已知作用机制相同的分子。阿司匹林对血小板 mRNA 的作用与基线和阿司匹林暴露后的血小板功能水平升高相关,这一作用与阿司匹林已知的抗血小板作用相抵消。总之,这项工作共同证明了阿司匹林对血小板转录组的剂量独立作用,这种作用与阿司匹林已知的抗血小板作用相抵消。