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Single Cell RNA Sequencing in Atherosclerosis Research.单细胞 RNA 测序在动脉粥样硬化研究中的应用。
Circ Res. 2020 Apr 24;126(9):1112-1126. doi: 10.1161/CIRCRESAHA.119.315940. Epub 2020 Apr 23.
2
Macrophage-Enriched lncRNA RAPIA: A Novel Therapeutic Target for Atherosclerosis.富含巨噬细胞的 lncRNA RAPIA:动脉粥样硬化的新治疗靶点。
Arterioscler Thromb Vasc Biol. 2020 Jun;40(6):1464-1478. doi: 10.1161/ATVBAHA.119.313749. Epub 2020 Apr 9.
3
Pervasive functional translation of noncanonical human open reading frames.广泛存在的非规范人类开放阅读框的功能翻译。
Science. 2020 Mar 6;367(6482):1140-1146. doi: 10.1126/science.aay0262.
4
Long noncoding RNA integrates a DNA-PK-mediated DNA damage response and vascular senescence.长非编码 RNA 整合了 DNA-PK 介导的 DNA 损伤反应和血管衰老。
Sci Transl Med. 2020 Feb 19;12(531). doi: 10.1126/scitranslmed.aaw1868.
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LncRNA TUG1 regulates proliferation and apoptosis by regulating miR-148b/IGF2 axis in ox-LDL-stimulated VSMC and HUVEC.长链非编码 RNA TUG1 通过调节 ox-LDL 刺激的血管平滑肌细胞和脐静脉内皮细胞中的 miR-148b/IGF2 轴来调节增殖和凋亡。
Life Sci. 2020 Feb 15;243:117287. doi: 10.1016/j.lfs.2020.117287. Epub 2020 Jan 8.
6
Knockdown of GAS5 Inhibits Atherosclerosis Progression via Reducing EZH2-Mediated ABCA1 Transcription in ApoE Mice.敲低GAS5通过降低EZH2介导的载脂蛋白E基因敲除小鼠中ABCA1转录来抑制动脉粥样硬化进展。
Mol Ther Nucleic Acids. 2020 Mar 6;19:84-96. doi: 10.1016/j.omtn.2019.10.034. Epub 2019 Nov 12.
7
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Effect of 1 or 2 Doses of Inclisiran on Low-Density Lipoprotein Cholesterol Levels: One-Year Follow-up of the ORION-1 Randomized Clinical Trial.依洛尤单抗 1 或 2 剂对低密度脂蛋白胆固醇水平的影响:ORION-1 随机临床试验的 1 年随访结果。
JAMA Cardiol. 2019 Nov 1;4(11):1067-1075. doi: 10.1001/jamacardio.2019.3502.
10
Silencing of GAS5 represses the malignant progression of atherosclerosis through upregulation of miR-135a.沉默 GAS5 通过上调 miR-135a 抑制动脉粥样硬化的恶性进展。
Biomed Pharmacother. 2019 Oct;118:109302. doi: 10.1016/j.biopha.2019.109302. Epub 2019 Aug 21.

长链非编码 RNA 在动脉粥样硬化和血管损伤中的作用:病理生物学、生物标志物和治疗靶点。

Long Noncoding RNAs in Atherosclerosis and Vascular Injury: Pathobiology, Biomarkers, and Targets for Therapy.

机构信息

From the Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA (J.B.P., M.W.F.).

Feinberg School of Medicine, Northwestern University, Chicago, IL (J.B.P.).

出版信息

Arterioscler Thromb Vasc Biol. 2020 Sep;40(9):2002-2017. doi: 10.1161/ATVBAHA.120.314222. Epub 2020 Jul 23.

DOI:10.1161/ATVBAHA.120.314222
PMID:32698685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7484026/
Abstract

Despite major advances in the primary and secondary prevention of atherosclerosis and its risk factors, atherosclerotic cardiovascular disease remains a major clinical and financial burden on individuals and health systems worldwide. In addition, neointima formation and proliferation due to mechanical trauma to the vessel wall during percutaneous coronary interventions can lead to vascular restenosis and limit the longevity and effectiveness of coronary revascularization. Long noncoding RNAs (lncRNAs) have emerged as a novel class of epigenetic regulators with critical roles in the pathogenesis of atherosclerosis and restenosis following vascular injury. Here, we provide an in-depth review of lncRNAs that regulate the development of atherosclerosis or contribute to the pathogenesis of restenosis following mechanical vascular injury. We describe the diverse array of intracellular mechanisms by which lncRNAs exert their regulatory effects. We highlight the utility and challenges of lncRNAs as biomarkers. Finally, we discuss the immense translational potential of lncRNAs and strategies for targeting them therapeutically using oligonucleotide-based therapeutics and novel gene therapy platforms.

摘要

尽管在动脉粥样硬化及其危险因素的一级和二级预防方面取得了重大进展,但动脉粥样硬化性心血管疾病仍然是全球个人和卫生系统的主要临床和经济负担。此外,经皮冠状动脉介入治疗时血管壁的机械性创伤会导致新生内膜形成和增殖,从而导致血管再狭窄,并限制冠状动脉血运重建的长期效果和有效性。长链非编码 RNA(lncRNA)作为一类新型表观遗传调控因子而出现,其在动脉粥样硬化的发病机制以及血管损伤后的再狭窄中具有关键作用。在这里,我们深入综述了调节动脉粥样硬化发展或有助于机械性血管损伤后再狭窄发病机制的 lncRNA。我们描述了 lncRNA 发挥其调节作用的多种细胞内机制。我们强调了 lncRNA 作为生物标志物的实用性和挑战。最后,我们讨论了 lncRNA 的巨大转化潜力,以及使用基于寡核苷酸的治疗方法和新型基因治疗平台靶向治疗它们的策略。