Bhass Samyukta, Banerjee Moinak
Human Molecular Genetics Lab, Neurobiology and Genetics Division, BRIC-Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram 695014, India.
BRIC-Regional Centre for Biotechnology, NCR Biotech Science Cluster, Faridabad 121001, India.
Cells. 2025 Aug 31;14(17):1359. doi: 10.3390/cells14171359.
Antihypertensive drugs are widely used for the treatment of hypertension, and the choice of drug and dosage is based on trial and error. The variability in drug response and adverse reactions leads to the poor adherence to treatment. Epigenetic modulation is one of the major mechanisms that may contribute to the variability in drug responses, and microRNAs (miRNAs) can serve as crucial epigenetic regulators and have also been reported to be associated with hypertension pathogenesis. The objective of this study is to investigate the regulatory effects of commonly used antihypertensive drugs on the endothelial miRNome in human aortic endothelial cells. We aim to integrate miRNA expression data with proteomic analyses to elucidate drug-induced molecular mechanisms relevant to hypertension treatment. Whole genome small RNA sequencing was performed, followed by whole proteome analysis using LC-MS/MS comparing between control and treated samples. The treatments induced significant differential regulation of several miRNAs and proteins; among these, a few reflected reverse relationships with miRNA regulation and protein expression. Certain miRNAs and their corresponding target proteins seem to distinguish between good therapeutic outcomes and potential side effects. This study unravels the potential role of drug-induced miRNAs in inducing post-transcriptional modifications to cause the differential expression of certain proteins that may induce not only therapeutic effects or drug side effects but can also indicate the potential for drug-repurposing in other diseases.
抗高血压药物被广泛用于治疗高血压,药物和剂量的选择基于反复试验。药物反应和不良反应的变异性导致治疗依从性差。表观遗传调控是可能导致药物反应变异性的主要机制之一,而微小RNA(miRNA)可作为关键的表观遗传调节因子,并且也已报道其与高血压发病机制有关。本研究的目的是研究常用抗高血压药物对人主动脉内皮细胞中内皮miRNA组的调节作用。我们旨在将miRNA表达数据与蛋白质组学分析相结合,以阐明与高血压治疗相关的药物诱导分子机制。进行了全基因组小RNA测序,随后使用LC-MS/MS对对照样品和处理样品进行全蛋白质组分析。这些处理诱导了几种miRNA和蛋白质的显著差异调节;其中,一些反映了与miRNA调节和蛋白质表达的反向关系。某些miRNA及其相应的靶蛋白似乎可以区分良好的治疗效果和潜在的副作用。本研究揭示了药物诱导的miRNA在诱导转录后修饰以导致某些蛋白质差异表达方面的潜在作用,这些蛋白质不仅可能诱导治疗效果或药物副作用,还可以表明在其他疾病中药物重新利用的潜力。