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靶向治疗主动脉瘤和夹层中的自噬作用。

Targeting autophagy in aortic aneurysm and dissection.

机构信息

Division of Cardiothoracic and Vascular Surgery, Sino-Swiss Heart-Lung Transplantation Institute, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Division of Cardiothoracic and Vascular Surgery, Sino-Swiss Heart-Lung Transplantation Institute, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China; Key Laboratory of Organ Transplantation, Ministry of Education; NHC Key Laboratory of Organ Transplantation; Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Wuhan, Hubei, China.

出版信息

Biomed Pharmacother. 2022 Sep;153:113547. doi: 10.1016/j.biopha.2022.113547. Epub 2022 Aug 15.

DOI:10.1016/j.biopha.2022.113547
PMID:36076620
Abstract

Autophagy is a well-conserved biological process that maintains homeostasis. Accumulating evidence has revealed that autophagy plays an important role in various cardiovascular diseases, such as aneurysm, aortic dissection, atherosclerosis, and myocardial ischemia-reperfusion injury. Here, we summarize the current experimental evidence on the function of autophagy and autophagy proteins in aortic aneurysm and dissection (AAD). AAD is a very serious aortic disease, and there are currently no effective drug treatment options. Studies have shown that autophagy is activated during AAD. However, the role of autophagy in AAD is still controversial. For example, knocking out autophagy related 5 (ATG5) or ATG7 to inhibit autophagy and excessive autophagy activation can promote the occurrence of AAD. Recently, multiple studies have demonstrated that rapamycin and metformin, which are autophagy activators, can delay the progression of AAD. Thus, targeting autophagy has the potential to become a new therapeutic strategy for AAD. In addition, we discuss the recent research progress on AAD from the perspective of single-cell RNA sequencing. Moreover, we offer our perspective on current challenges and barriers in this research field.

摘要

自噬是一种广泛存在的生物过程,可维持体内平衡。越来越多的证据表明,自噬在各种心血管疾病中发挥着重要作用,如动脉瘤、主动脉夹层、动脉粥样硬化和心肌缺血再灌注损伤。在这里,我们总结了自噬及其相关蛋白在腹主动脉瘤和夹层(AAD)中的作用的最新实验证据。AAD 是一种非常严重的主动脉疾病,目前尚无有效的药物治疗选择。研究表明,AAD 期间自噬被激活。然而,自噬在 AAD 中的作用仍存在争议。例如,敲除自噬相关 5(ATG5)或 ATG7 以抑制自噬和过度自噬激活可以促进 AAD 的发生。最近,多项研究表明,自噬激活剂雷帕霉素和二甲双胍可延缓 AAD 的进展。因此,靶向自噬有可能成为 AAD 的一种新的治疗策略。此外,我们还从单细胞 RNA 测序的角度讨论了 AAD 的最新研究进展。此外,我们还提供了对该研究领域当前挑战和障碍的看法。

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Targeting autophagy in aortic aneurysm and dissection.靶向治疗主动脉瘤和夹层中的自噬作用。
Biomed Pharmacother. 2022 Sep;153:113547. doi: 10.1016/j.biopha.2022.113547. Epub 2022 Aug 15.
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Long non‑coding RNA SNHG1 promotes autophagy in vascular smooth muscle cells induced by facilitating CLEC7A.长链非编码 RNA SNHG1 通过促进 CLEC7A 促进血管平滑肌细胞自噬。
Mol Med Rep. 2025 Jan;31(1). doi: 10.3892/mmr.2024.13385. Epub 2024 Nov 8.
2
The roles of METTL3 on autophagy and proliferation of vascular smooth muscle cells are mediated by mTOR rather than by CDK1.METTL3对血管平滑肌细胞自噬和增殖的作用是由mTOR而非CDK1介导的。
Cell Div. 2023 Aug 9;18(1):13. doi: 10.1186/s13008-023-00096-5.
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The epigenetic regulatory mechanisms of ferroptosis and its implications for biological processes and diseases.
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MedComm (2020). 2023 May 22;4(3):e267. doi: 10.1002/mco2.267. eCollection 2023 Jun.
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Tandem mass tag-based quantitative proteomic analysis identification of succinylation related proteins in pathogenesis of thoracic aortic aneurysm and aortic dissection.基于串联质量标签的定量蛋白质组学分析鉴定胸主动脉瘤和主动脉夹层发病机制中的琥珀酰化相关蛋白。
PeerJ. 2023 May 11;11:e15258. doi: 10.7717/peerj.15258. eCollection 2023.