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肌微RNA-133a-3p、-133b和-206失调在心血管疾病风险中的潜在作用

The Potential Contribution of MyomiRs miR-133a-3p, -133b, and -206 Dysregulation in Cardiovascular Disease Risk.

作者信息

Crocco Paolina, Montesanto Alberto, La Grotta Rossella, Paparazzo Ersilia, Soraci Luca, Dato Serena, Passarino Giuseppe, Rose Giuseppina

机构信息

Department of Biology, Ecology and Earth Sciences, University of Calabria, 87036 Rende, Italy.

Unit of Geriatric Medicine, Italian National Research Center on Aging (INRCA-IRCCS), 87100 Cosenza, Italy.

出版信息

Int J Mol Sci. 2024 Nov 27;25(23):12772. doi: 10.3390/ijms252312772.

Abstract

Cardiovascular disease (CVD) is a major global health concern. The number of people with CVD is expected to rise due to aging populations and increasing risk factors such as obesity and diabetes. Identifying new molecular markers is crucial for early diagnosis and treatment. Among these, plasma levels of some miRNAs, specifically expressed in cardiac and skeletal muscle, known as myomiRs, have gained attention for their roles in cardiovascular health. This study analyzed the plasma levels of miR-133a-3p, -133b, and -206 in the pathogenesis of cardiovascular diseases. Using a case-control study design with patients recruited from several nursing homes from Calabria (southern Italy) characterized by different types of CVD compared with non-CVD controls, we found downregulation of miR-133a-3p in heart failure and miR-133b in stroke, along with the overall decreased expression of miR-133b and miR-206 in CVD patients, although they showed low specificity as biomarkers of CVD (as based on ROC analysis). In silico functional characterization of their targets and signaling pathways revealed their involvement in critical cardiovascular processes. Although further research is necessary to fully elucidate their mechanisms and clinical utility, the findings reported here may provide insight into the potential contribution of myomiRs in the cardiovascular injury framework, also offering indications for new research directions.

摘要

心血管疾病(CVD)是全球主要的健康问题。由于人口老龄化以及肥胖和糖尿病等风险因素的增加,心血管疾病患者的数量预计将会上升。识别新的分子标志物对于早期诊断和治疗至关重要。其中,一些在心肌和骨骼肌中特异性表达的微小RNA(miRNA),即肌微小RNA(myomiR),因其在心血管健康中的作用而受到关注。本研究分析了miR-133a-3p、-133b和-206在心血管疾病发病机制中的血浆水平。采用病例对照研究设计,从意大利南部卡拉布里亚的几家疗养院招募患者,这些患者患有不同类型的心血管疾病,并与非心血管疾病对照组进行比较。我们发现,心力衰竭患者中miR-133a-3p下调,中风患者中miR-133b下调,并且心血管疾病患者中miR-133b和miR-206的总体表达降低,尽管它们作为心血管疾病生物标志物的特异性较低(基于ROC分析)。对其靶标和信号通路的计算机功能表征揭示了它们参与关键的心血管过程。尽管需要进一步研究以充分阐明其机制和临床应用,但此处报道的研究结果可能为肌微小RNA在心血管损伤框架中的潜在作用提供见解,也为新的研究方向提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2c/11641116/bbad0495d752/ijms-25-12772-g001.jpg

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