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FoxO1-miRNA 相互作用网络作为线粒体疾病的潜在靶点。

FoxO1-miRNA interacting networks as potential targets for mitochondrial diseases.

机构信息

Department of Pharmacology, College of Graduate Studies, Midwestern University, Downers Grove, IL, USA.

出版信息

Drug Discov Today. 2019 Jan;24(1):342-349. doi: 10.1016/j.drudis.2018.10.011. Epub 2018 Oct 24.

Abstract

Mitochondrial homeostasis is important for the health and well-being of organ systems and organisms. Mitochondrial dysfunction is known to be the cause and consequence of metabolic diseases, including obesity, diabetes, cancer, neurodegeneration, cerebrovascular, and cardiovascular disease. For cardiovascular tissue, which relies mostly on oxidative phosphorylation, the role of mitochondria is inevitable. Rather than being biomarkers of mitochondrial health, miRNAs are now known as bioregulators of this important feature. Recent studies have shown a close interaction between Forkhead box other 1 (FoxO1) transcription factors and miRNAs in the cardiovascular system. These interactions have also been shown to regulate mitochondrial homeostasis. In this review, I highlight how understanding FoxO1 and miRNA interacting networks could enable us to limit mitochondrial dysfunction and associated pathologies.

摘要

线粒体动态平衡对于器官系统和生物体的健康和幸福至关重要。线粒体功能障碍是代谢疾病(包括肥胖、糖尿病、癌症、神经退行性疾病、脑血管和心血管疾病)的原因和后果。对于主要依赖氧化磷酸化的心血管组织来说,线粒体的作用是不可或缺的。miRNA 不再被视为线粒体健康的生物标志物,而是这种重要特性的生物调节剂。最近的研究表明,叉头框转录因子 O1(FoxO1)和心血管系统中的 miRNA 之间存在密切的相互作用。这些相互作用也被证明可以调节线粒体动态平衡。在这篇综述中,我强调了理解 FoxO1 和 miRNA 相互作用网络如何使我们能够限制线粒体功能障碍和相关病理的发生。

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