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Krüppel 样因子 5(KLF5):心血管健康的新兴敌人。

Krüppel-like factor (KLF)5: An emerging foe of cardiovascular health.

机构信息

Center for Translational Medicine, Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA; School of Biology, Aristotle University of Thessaloniki, GR, Greece.

School of Biology, Aristotle University of Thessaloniki, GR, Greece.

出版信息

J Mol Cell Cardiol. 2022 Feb;163:56-66. doi: 10.1016/j.yjmcc.2021.10.002. Epub 2021 Oct 13.

Abstract

Krüppel-like factors (KLFs) are DNA-binding transcriptional factors, which regulate various pathways that pertain to development, metabolism and other cellular mechanisms. KLF5 was first cloned in 1993 and by 1999, it was reported as the intestinal-enriched KLF. Beyond findings that have associated KLF5 with normal development and cancer, it has been associated with various types of cardiovascular (CV) complications and regulation of metabolic pathways in the liver, heart, adipose tissue and skeletal muscle. Specifically, increased KLF5 expression has been linked with cardiomyopathy in diabetes, end-stage heart failure, and as well as in vascular atherosclerotic lesions. In this review article, we summarize research findings about transcriptional, post-transcriptional and post-translational regulation of KLF5, as well as the role of KLF5 in the biology of cells and organs that affect cardiovascular health either directly or indirectly. Finally, we propose KLF5 inhibition as an emerging approach for cardiovascular therapeutics.

摘要

Krüppel 样因子 (KLFs) 是 DNA 结合转录因子,可调节与发育、代谢和其他细胞机制相关的各种途径。KLF5 于 1993 年首次被克隆,到 1999 年,它被报道为肠丰富的 KLF。除了发现 KLF5 与正常发育和癌症有关外,它还与各种类型的心血管 (CV) 并发症以及肝脏、心脏、脂肪组织和骨骼肌中的代谢途径调节有关。具体而言,KLF5 表达增加与糖尿病心肌病、终末期心力衰竭以及血管动脉粥样硬化病变有关。在这篇综述文章中,我们总结了关于 KLF5 的转录、转录后和翻译后调节的研究结果,以及 KLF5 在影响心血管健康的细胞和器官生物学中的作用,无论是直接还是间接。最后,我们提出 KLF5 抑制作为心血管治疗的一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eda9/8816822/6ec235d67f22/nihms-1750729-f0002.jpg

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