• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于非编码 RNA 治疗剂的靶向递呈在动脉粥样硬化中的最新进展。

Recent advances in targeted delivery of non-coding RNA-based therapeutics for atherosclerosis.

机构信息

Center for Regenerative Medicine, Institute for Translational Medicine, The Affiliated Hospital of Qingdao University, No. 38 Dengzhou Road, Qingdao 266021, People's Republic of China.

Department of Cardiology, People's Hospital of Rizhao, No. 126 Taian Road, Rizhao 276827, People's Republic of China.

出版信息

Mol Ther. 2022 Oct 5;30(10):3118-3132. doi: 10.1016/j.ymthe.2022.07.018. Epub 2022 Aug 1.

DOI:10.1016/j.ymthe.2022.07.018
PMID:35918894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9552813/
Abstract

Cardiovascular disease (CVD) has overtaken infectious illnesses as the leading cause of mortality and disability worldwide. The pathology that underpins CVD is atherosclerosis, characterized by chronic inflammation caused by the accumulation of plaques in the arteries. As our knowledge about the microenvironment of blood vessel walls deepens, there is an opportunity to fine-tune treatments to target the mechanisms driving atherosclerosis more directly. The application of non-coding RNAs (ncRNAs) as biomarkers or intervention targets is increasing. Although these ncRNAs play an important role in driving atherosclerosis and vascular dysfunction, the cellular and extracellular environments pose a challenge for targeted transmission and therapeutic regulation of ncRNAs. Specificity, delivery, and tolerance have hampered the clinical translation of ncRNA-based therapeutics. Nanomedicine is an emerging field that uses nanotechnology for targeted drug delivery and advanced imaging. Recently, nanoscale carriers have shown promising results and have introduced new possibilities for nucleic acid targeted drug delivery, particularly for atherosclerosis. In this review, we discuss the latest developments in nanoparticles to aid ncRNA-based drug development, particularly miRNA, and we analyze the current challenges in ncRNA targeted delivery. In particular, we highlight the emergence of various kinds of nanotherapeutic approaches based on ncRNAs, which can improve treatment options for atherosclerosis.

摘要

心血管疾病 (CVD) 已超过传染病成为全球死亡和残疾的主要原因。CVD 的病理学基础是动脉粥样硬化,其特征是斑块在动脉中的积累引起的慢性炎症。随着我们对血管壁微环境的了解加深,有机会更直接地针对导致动脉粥样硬化的机制来调整治疗方法。非编码 RNA (ncRNA) 作为生物标志物或干预靶点的应用正在增加。虽然这些 ncRNA 在驱动动脉粥样硬化和血管功能障碍方面发挥着重要作用,但细胞和细胞外环境对 ncRNA 的靶向传递和治疗调节构成了挑战。特异性、传递和耐受性阻碍了基于 ncRNA 的治疗的临床转化。纳米医学是一个新兴领域,利用纳米技术进行靶向药物传递和高级成像。最近,纳米载体显示出有希望的结果,并为核酸靶向药物传递带来了新的可能性,特别是在动脉粥样硬化方面。在这篇综述中,我们讨论了用于辅助基于 ncRNA 的药物开发的纳米颗粒的最新进展,特别是 miRNA,并分析了 ncRNA 靶向传递的当前挑战。特别地,我们强调了基于 ncRNA 的各种新型治疗方法的出现,这可以改善动脉粥样硬化的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/9552813/2e8d5a2b88c3/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/9552813/2e8d5a2b88c3/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/88ca/9552813/2e8d5a2b88c3/fx1.jpg

相似文献

1
Recent advances in targeted delivery of non-coding RNA-based therapeutics for atherosclerosis.基于非编码 RNA 治疗剂的靶向递呈在动脉粥样硬化中的最新进展。
Mol Ther. 2022 Oct 5;30(10):3118-3132. doi: 10.1016/j.ymthe.2022.07.018. Epub 2022 Aug 1.
2
ncRNAs in Therapeutics: Challenges and Limitations in Nucleic Acid-Based Drug Delivery.ncRNAs 在治疗中的应用:基于核酸的药物递送的挑战和局限性。
Int J Mol Sci. 2021 Oct 27;22(21):11596. doi: 10.3390/ijms222111596.
3
Nanomedicine Meets microRNA: Current Advances in RNA-Based Nanotherapies for Atherosclerosis.纳米医学与微小RNA:基于RNA的动脉粥样硬化纳米疗法的当前进展
Arterioscler Thromb Vasc Biol. 2016 Sep;36(9):e73-9. doi: 10.1161/ATVBAHA.116.307481.
4
Non-Coding RNA-Targeted Therapy: A State-of-the-Art Review.非编码 RNA 靶向治疗:最新综述。
Int J Mol Sci. 2024 Mar 24;25(7):3630. doi: 10.3390/ijms25073630.
5
Strategies and challenges for non-viral delivery of non-coding RNAs to the heart.非编码RNA心脏非病毒递送的策略与挑战
Trends Mol Med. 2023 Jan;29(1):70-91. doi: 10.1016/j.molmed.2022.10.002. Epub 2022 Nov 9.
6
Decoding microRNA drivers in atherosclerosis.解析动脉粥样硬化中的 microRNA 调控因子
Biosci Rep. 2022 Jul 29;42(7). doi: 10.1042/BSR20212355.
7
Systematic review regulatory principles of non-coding RNAs in cardiovascular diseases.系统评价非编码 RNA 在心血管疾病中的调控原则。
Brief Bioinform. 2019 Jan 18;20(1):66-76. doi: 10.1093/bib/bbx095.
8
Non-coding RNAs in cardiovascular cell biology and atherosclerosis.非编码 RNA 在心血管细胞生物学和动脉粥样硬化中的作用。
Cardiovasc Res. 2019 Oct 1;115(12):1732-1756. doi: 10.1093/cvr/cvz203.
9
Non-coding RNAs regulating mitochondrial function in cardiovascular diseases.非编码 RNA 调控心血管疾病中线粒体功能。
J Mol Med (Berl). 2023 May;101(5):501-526. doi: 10.1007/s00109-023-02305-8. Epub 2023 Apr 4.
10
Pyroptosis-related non-coding RNAs emerging players in atherosclerosis pathology.焦亡相关非编码RNA:动脉粥样硬化病理中的新兴参与者
Pathol Res Pract. 2024 Mar;255:155219. doi: 10.1016/j.prp.2024.155219. Epub 2024 Feb 16.

引用本文的文献

1
Extracellular Vesicles-in-Hydrogel (EViH) targeting pathophysiology for tissue repair.用于组织修复的靶向病理生理学的水凝胶包裹细胞外囊泡(EViH)
Bioact Mater. 2024 Oct 23;44:283-318. doi: 10.1016/j.bioactmat.2024.10.017. eCollection 2025 Feb.
2
Autophagy-associated non-coding RNAs: Unraveling their impact on Parkinson's disease pathogenesis.自噬相关非编码 RNA:揭示其对帕金森病发病机制的影响。
CNS Neurosci Ther. 2024 May;30(5):e14763. doi: 10.1111/cns.14763.
3
Intracranial aneurysm circulating exosome-derived LncRNA ATP1A1-AS1 promotes smooth muscle cells phenotype switching and apoptosis.

本文引用的文献

1
miR-564: A potential regulator of vascular smooth muscle cells and therapeutic target for aortic dissection.miR-564:血管平滑肌细胞的潜在调节剂和主动脉夹层的治疗靶点。
J Mol Cell Cardiol. 2022 Sep;170:100-114. doi: 10.1016/j.yjmcc.2022.06.003. Epub 2022 Jun 18.
2
The lncRNA Punisher Regulates Apoptosis and Mitochondrial Homeostasis of Vascular Smooth Muscle Cells via Targeting miR-664a-5p and OPA1.长链非编码 RNA Punisher 通过靶向 miR-664a-5p 和 OPA1 调控血管平滑肌细胞凋亡和线粒体稳态。
Oxid Med Cell Longev. 2022 May 25;2022:5477024. doi: 10.1155/2022/5477024. eCollection 2022.
3
Butorphanol Suppresses the Proliferation and Migration of Osteosarcoma by Promoting the Expression of piRNA hsa_piR_006613.
颅内动脉瘤循环外泌体源性长非编码 RNA ATP1A1-AS1 促进平滑肌细胞表型转换和凋亡。
Aging (Albany NY). 2024 May 8;16(9):8320-8335. doi: 10.18632/aging.205821.
4
CircHIPK3 targets DRP1 to mediate hydrogen peroxide-induced necroptosis of vascular smooth muscle cells and atherosclerotic vulnerable plaque formation.环状HIPK3靶向动力相关蛋白1以介导过氧化氢诱导的血管平滑肌细胞坏死性凋亡及动脉粥样硬化易损斑块形成。
J Adv Res. 2025 Mar;69:329-341. doi: 10.1016/j.jare.2024.04.011. Epub 2024 Apr 15.
5
BioDeepfuse: a hybrid deep learning approach with integrated feature extraction techniques for enhanced non-coding RNA classification.BioDeepfuse:一种混合深度学习方法,结合了集成特征提取技术,用于增强非编码 RNA 分类。
RNA Biol. 2024 Jan;21(1):1-12. doi: 10.1080/15476286.2024.2329451. Epub 2024 Mar 25.
6
The role and medical prospects of long non-coding RNAs in cardiovascular disease.长链非编码 RNA 在心血管疾病中的作用和医学前景。
Heart Fail Rev. 2023 Nov;28(6):1437-1453. doi: 10.1007/s10741-023-10342-1. Epub 2023 Oct 5.
7
Functions and mechanisms of protein lysine butyrylation (Kbu): Therapeutic implications in human diseases.蛋白质赖氨酸丁酰化(Kbu)的功能与机制:对人类疾病的治疗意义
Genes Dis. 2022 Nov 29;10(6):2479-2490. doi: 10.1016/j.gendis.2022.10.025. eCollection 2023 Nov.
8
Super-enhancer-driven lncRNA LIMD1-AS1 activated by CDK7 promotes glioma progression.超级增强子驱动的长链非编码 RNA LIMD1-AS1 被 CDK7 激活,促进胶质瘤进展。
Cell Death Dis. 2023 Jun 29;14(6):383. doi: 10.1038/s41419-023-05892-z.
9
Molecular imaging research in atherosclerosis: A 23-year scientometric and visual analysis.动脉粥样硬化的分子成像研究:一项为期23年的科学计量学与可视化分析
Front Bioeng Biotechnol. 2023 Apr 13;11:1152067. doi: 10.3389/fbioe.2023.1152067. eCollection 2023.
10
Protective effect and mechanism of ginsenoside Rg2 on atherosclerosis.人参皂苷Rg2对动脉粥样硬化的保护作用及机制
J Ginseng Res. 2023 Mar;47(2):237-245. doi: 10.1016/j.jgr.2022.08.001. Epub 2022 Aug 6.
布托啡诺通过促进piRNA hsa_piR_006613的表达来抑制骨肉瘤的增殖和迁移。
Front Oncol. 2022 Feb 24;12:775132. doi: 10.3389/fonc.2022.775132. eCollection 2022.
4
Comprehensive profile of circRNAs in formaldehyde induced heart development.甲醛诱导心脏发育过程中环状RNA的综合概况
Food Chem Toxicol. 2022 Apr;162:112899. doi: 10.1016/j.fct.2022.112899. Epub 2022 Feb 26.
5
Heart Disease and Stroke Statistics-2022 Update: A Report From the American Heart Association.《心脏病与卒中统计-2022 更新:美国心脏协会报告》。
Circulation. 2022 Feb 22;145(8):e153-e639. doi: 10.1161/CIR.0000000000001052. Epub 2022 Jan 26.
6
Drug delivery systems for RNA therapeutics.RNA 治疗药物的递药系统。
Nat Rev Genet. 2022 May;23(5):265-280. doi: 10.1038/s41576-021-00439-4. Epub 2022 Jan 4.
7
Multistage-Responsive Nanocomplexes Attenuate Ulcerative Colitis by Improving the Accumulation and Distribution of Oral Nucleic Acid Drugs in the Colon.多阶段响应型纳米复合物通过改善口服核酸药物在结肠中的积累和分布来减轻溃疡性结肠炎。
ACS Appl Mater Interfaces. 2022 Jan 12;14(1):2058-2070. doi: 10.1021/acsami.1c21595. Epub 2022 Jan 3.
8
CircNPHP4 in monocyte-derived small extracellular vesicles controls heterogeneous adhesion in coronary heart atherosclerotic disease.CircNPHP4 在单核细胞衍生的小细胞外囊泡中控制冠心病动脉粥样硬化疾病中的异质性黏附。
Cell Death Dis. 2021 Oct 14;12(10):948. doi: 10.1038/s41419-021-04253-y.
9
Macrophage NFATc3 prevents foam cell formation and atherosclerosis: evidence and mechanisms.巨噬细胞 NFATc3 可防止泡沫细胞形成和动脉粥样硬化:证据和机制。
Eur Heart J. 2021 Dec 14;42(47):4847-4861. doi: 10.1093/eurheartj/ehab660.
10
Computational methods for RNA modification detection from nanopore direct RNA sequencing data.基于纳米孔直接 RNA 测序数据的 RNA 修饰检测的计算方法。
RNA Biol. 2021 Oct 15;18(sup1):31-40. doi: 10.1080/15476286.2021.1978215. Epub 2021 Sep 24.