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长链非编码 RNA 在糖尿病相关外周动脉疾病中的作用。

Role of long noncoding RNAs in diabetes-associated peripheral arterial disease.

机构信息

Irell and Manella Graduate School of Biological Sciences, City of Hope, Duarte, CA, 91010, USA.

Department of Diabetes Complications and Metabolism, Arthur Riggs Diabetes and Metabolism Research Institute, City of Hope, Duarte, CA, USA.

出版信息

Cardiovasc Diabetol. 2024 Jul 24;23(1):274. doi: 10.1186/s12933-024-02327-7.


DOI:10.1186/s12933-024-02327-7
PMID:39049097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11271017/
Abstract

Diabetes mellitus (DM) is a metabolic disease that heightens the risks of many vascular complications, including peripheral arterial disease (PAD). Various types of cells, including but not limited to endothelial cells (ECs), vascular smooth muscle cells (VSMCs), and macrophages (MΦs), play crucial roles in the pathogenesis of DM-PAD. Long non-coding RNAs (lncRNAs) are epigenetic regulators that play important roles in cellular function, and their dysregulation in DM can contribute to PAD. This review focuses on the developing field of lncRNAs and their emerging roles in linking DM and PAD. We review the studies investigating the role of lncRNAs in crucial cellular processes contributing to DM-PAD, including those in ECs, VSMCs, and MΦ. By examining the intricate molecular landscape governed by lncRNAs in these relevant cell types, we hope to shed light on the roles of lncRNAs in EC dysfunction, inflammatory responses, and vascular remodeling contributing to DM-PAD. Additionally, we provide an overview of the research approach and methodologies, from identifying disease-relevant lncRNAs to characterizing their molecular and cellular functions in the context of DM-PAD. We also discuss the potential of leveraging lncRNAs in the diagnosis and therapeutics for DM-PAD. Collectively, this review provides a summary of lncRNA-regulated cell functions contributing to DM-PAD and highlights the translational potential of leveraging lncRNA biology to tackle this increasingly prevalent and complex disease.

摘要

糖尿病(DM)是一种代谢性疾病,会增加许多血管并发症的风险,包括外周动脉疾病(PAD)。各种类型的细胞,包括但不限于内皮细胞(ECs)、血管平滑肌细胞(VSMCs)和巨噬细胞(MΦs),在 DM-PAD 的发病机制中发挥着关键作用。长链非编码 RNA(lncRNAs)是表观遗传调节剂,在细胞功能中发挥着重要作用,它们在 DM 中的失调可能导致 PAD。本综述重点介绍 lncRNAs 的新兴领域及其在连接 DM 和 PAD 中的作用。我们综述了研究 lncRNAs 在导致 DM-PAD 的关键细胞过程中的作用的研究,包括在 ECs、VSMCs 和 MΦ 中的作用。通过研究这些相关细胞类型中由 lncRNAs 调控的复杂分子景观,我们希望阐明 lncRNAs 在 EC 功能障碍、炎症反应和血管重塑中导致 DM-PAD 的作用。此外,我们还概述了研究方法和方法,从鉴定与疾病相关的 lncRNAs 到描述它们在 DM-PAD 背景下的分子和细胞功能。我们还讨论了利用 lncRNAs 进行 DM-PAD 的诊断和治疗的潜力。总之,本综述总结了 lncRNA 调控的细胞功能在导致 DM-PAD 中的作用,并强调了利用 lncRNA 生物学解决这种日益普遍和复杂疾病的转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcd6/11271017/40068aec7176/12933_2024_2327_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcd6/11271017/ceddf9df6c2a/12933_2024_2327_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcd6/11271017/40068aec7176/12933_2024_2327_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcd6/11271017/ceddf9df6c2a/12933_2024_2327_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcd6/11271017/40068aec7176/12933_2024_2327_Fig2_HTML.jpg

相似文献

[1]
Role of long noncoding RNAs in diabetes-associated peripheral arterial disease.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Non-coding RNAs to treat vascular smooth muscle cell dysfunction.

Br J Pharmacol. 2025-1

[2]
Control of endothelial cell function and arteriogenesis by MEG3:EZH2 epigenetic regulation of integrin expression.

Mol Ther Nucleic Acids. 2024-4-6

[3]
LncRNA CARMN inhibits abdominal aortic aneurysm formation and vascular smooth muscle cell phenotypic transformation by interacting with SRF.

Cell Mol Life Sci. 2024-4-10

[4]
Distinct Plasma Extracellular Vesicle Transcriptomes in Acute Decompensated Heart Failure Subtypes: A Liquid Biopsy Approach.

Circulation. 2024-4-2

[5]
Multifaceted roles of Meg3 in cellular senescence and atherosclerosis.

Atherosclerosis. 2024-5

[6]
Expression and diagnostic value of lncRNA MALAT1 and NLRP3 in lower limb atherosclerosis in diabetes.

BMC Endocr Disord. 2024-3-4

[7]
Deficiency of lncRNA MERRICAL abrogates macrophage chemotaxis and diabetes-associated atherosclerosis.

Cell Rep. 2024-3-26

[8]
Long noncoding RNA H19: functions and mechanisms in regulating programmed cell death in cancer.

Cell Death Discov. 2024-2-14

[9]
Epigenetic Regulation of Angiogenesis in Peripheral Artery Disease.

Methodist Debakey Cardiovasc J. 2023

[10]
lncRNA FAS-AS1 served as a diagnostic biomarker of end-stage renal disease and mediated vascular calcification via regulating oxidative stress and inflammation.

Gene. 2024-2-20

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