吸烟的微小RNA特征和微小RNA在吸烟相关炎症和靶器官损伤中可能起因果作用的证据。

Christine M Willinger, Jian Rong, Kahraman Tanriverdi, Paul L Courchesne, Tianxiao Huan, Gregory A Wasserman, Honghuang Lin, Josée Dupuis, Roby Joehanes, Matthew R Jones, George Chen, Emelia J Benjamin, George T O'Connor, Joseph P Mizgerd, Jane E Freedman, Martin G Larson, Daniel Levy
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引用次数: 0

摘要

背景:吸烟会增加患多种疾病的风险。微小RNA调节基因表达,可能在吸烟诱导的靶器官损伤中发挥作用。我们试图描述吸烟的微小RNA特征,并将其与吸烟相关的临床表型、基因表达和肺部炎症信号联系起来。方法和结果:使用TaqMan分析和高通量逆转录定量聚合酶链反应,对5023名Framingham心脏研究参与者(54.0%女性;平均年龄55±13岁)的全血来源RNA进行了283个微小RNA的表达谱分析。用线性混合效应模型测试了微小RNA表达与吸烟状态的相关性,以及吸烟相关微小RNA与炎症生物标志物和肺功能的相关性。我们鉴定了吸烟的6个微小核糖核酸特征。6个吸烟相关的微小RNA中有5个与血清C反应蛋白或白细胞介素-6水平相关;miR-1180与肺功能测量在一个边际显著水平上相关。对与吸烟的微小RNA特征共表达的吸烟相关基因的生物信息学评估揭示了免疫相关途径的富集。吸烟相关的微小RNA改变了细胞培养物功能获得测定中选定炎症介质的表达。结论:我们表征了吸烟的一种新的微小RNA特征。顶级微小RNA与全身炎症标志物和肺功能降低有关,与参与免疫功能的基因表达有关,并且足以调节炎症信号。我们的研究结果强调了吸烟相关的微小RNA,并与吸烟相关微小RNA作为吸烟诱导的炎症和靶器官损伤的介质的假设一致。这些发现需要进一步的机制研究来探索吸烟相关微小RNA的诊断和治疗用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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MicroRNA Signature of Cigarette Smoking and Evidence for a Putative Causal Role of MicroRNAs in Smoking-Related Inflammation and Target Organ Damage.

Background: Cigarette smoking increases risk for multiple diseases. MicroRNAs regulate gene expression and may play a role in smoking-induced target organ damage. We sought to describe a microRNA signature of cigarette smoking and relate it to smoking-associated clinical phenotypes, gene expression, and lung inflammatory signaling.

Methods and results: Expression profiling of 283 microRNAs was conducted on whole blood-derived RNA from 5023 Framingham Heart Study participants (54.0% women; mean age, 55±13 years) using TaqMan assays and high-throughput reverse transcription quantitative polymerase chain reaction. Associations of microRNA expression with smoking status and associations of smoking-related microRNAs with inflammatory biomarkers and pulmonary function were tested with linear mixed effects models. We identified a 6-microRNA signature of smoking. Five of the 6 smoking-related microRNAs were associated with serum levels of C-reactive protein or interleukin-6; miR-1180 was associated with pulmonary function measures at a marginally significant level. Bioinformatic evaluation of smoking-associated genes coexpressed with the microRNA signature of cigarette smoking revealed enrichment for immune-related pathways. Smoking-associated microRNAs altered expression of selected inflammatory mediators in cell culture gain-of-function assays.

Conclusions: We characterized a novel microRNA signature of cigarette smoking. The top microRNAs were associated with systemic inflammatory markers and reduced pulmonary function, correlated with expression of genes involved in immune function, and were sufficient to modulate inflammatory signaling. Our results highlight smoking-associated microRNAs and are consistent with the hypothesis that smoking-associated microRNAs serve as mediators of smoking-induced inflammation and target organ damage. These findings call for further mechanistic studies to explore the diagnostic and therapeutic use of smoking-related microRNAs.

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来源期刊
Circulation: Cardiovascular Genetics
Circulation: Cardiovascular Genetics CARDIAC & CARDIOVASCULAR SYSTEMS-GENETICS & HEREDITY
自引率
0.00%
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0
审稿时长
6-12 weeks
期刊介绍: Circulation: Genomic and Precision Medicine considers all types of original research articles, including studies conducted in human subjects, laboratory animals, in vitro, and in silico. Articles may include investigations of: clinical genetics as applied to the diagnosis and management of monogenic or oligogenic cardiovascular disorders; the molecular basis of complex cardiovascular disorders, including genome-wide association studies, exome and genome sequencing-based association studies, coding variant association studies, genetic linkage studies, epigenomics, transcriptomics, proteomics, metabolomics, and metagenomics; integration of electronic health record data or patient-generated data with any of the aforementioned approaches, including phenome-wide association studies, or with environmental or lifestyle factors; pharmacogenomics; regulation of gene expression; gene therapy and therapeutic genomic editing; systems biology approaches to the diagnosis and management of cardiovascular disorders; novel methods to perform any of the aforementioned studies; and novel applications of precision medicine. Above all, we seek studies with relevance to human cardiovascular biology and disease.
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