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细胞外囊泡促进血管损伤的基本发病机制和表观遗传调控因子。

Basic Pathogenic Mechanisms and Epigenetic Players Promoted by Extracellular Vesicles in Vascular Damage.

机构信息

Department of Advanced Medical and Surgical Sciences (DAMSS), University of Campania Luigi Vanvitelli, 80138 Naples, Italy.

Laboratory of Cellular and Molecular Cardiology, Cardiocentro Ticino Institute, 6807 Taverne-Torricella, Switzerland.

出版信息

Int J Mol Sci. 2023 Apr 19;24(8):7509. doi: 10.3390/ijms24087509.


DOI:10.3390/ijms24087509
PMID:37108672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10138986/
Abstract

Both progression from the early pathogenic events to clinically manifest cardiovascular diseases (CVD) and cancer impact the integrity of the vascular system. Pathological vascular modifications are affected by interplay between endothelial cells and their microenvironment. Soluble factors, extracellular matrix molecules and extracellular vesicles (EVs) are emerging determinants of this network that trigger specific signals in target cells. EVs have gained attention as package of molecules with epigenetic reversible activity causing functional vascular changes, but their mechanisms are not well understood. Valuable insights have been provided by recent clinical studies, including the investigation of EVs as potential biomarkers of these diseases. In this paper, we review the role and the mechanism of exosomal epigenetic molecules during the vascular remodeling in coronary heart disease as well as in cancer-associated neoangiogenesis.

摘要

从早期致病事件进展到临床表现的心血管疾病(CVD)和癌症都会影响血管系统的完整性。病理性血管改变受内皮细胞及其微环境之间的相互作用影响。可溶性因子、细胞外基质分子和细胞外囊泡(EVs)是该网络的新兴决定因素,它们在靶细胞中引发特定信号。EVs 作为具有表观遗传可逆活性的分子包引起功能性血管变化,因此备受关注,但它们的机制尚不清楚。最近的临床研究提供了有价值的见解,包括将 EVs 作为这些疾病潜在生物标志物的研究。本文综述了外泌体表观遗传分子在冠心病血管重构以及癌症相关新生血管形成中的作用和机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e11/10138986/fe09210ce36b/ijms-24-07509-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e11/10138986/49c6dff90d10/ijms-24-07509-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e11/10138986/fe09210ce36b/ijms-24-07509-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e11/10138986/49c6dff90d10/ijms-24-07509-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e11/10138986/fe09210ce36b/ijms-24-07509-g002.jpg

相似文献

[1]
Basic Pathogenic Mechanisms and Epigenetic Players Promoted by Extracellular Vesicles in Vascular Damage.

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[3]
Evolving Strategies for Extracellular Vesicles as Future Cardiac Therapeutics: From Macro- to Nano-Applications.

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[4]
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J Transl Med. 2024-5-17

[5]
Extracellular Vesicles in Atherosclerosis: State of the Art.

Int J Mol Sci. 2023-12-27

[6]
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本文引用的文献

[1]
Role of MSC-derived small extracellular vesicles in tissue repair and regeneration.

Front Cell Dev Biol. 2023-3-1

[2]
ADSC-derived exosomes attenuate myocardial infarction injury by promoting miR-205-mediated cardiac angiogenesis.

Biol Direct. 2023-2-27

[3]
Extracellular Non-Coding RNAs in Cardiovascular Diseases.

Pharmaceutics. 2023-1-3

[4]
Small extracellular vesicles in metabolic remodeling of tumor cells: Cargos and translational application.

Front Pharmacol. 2022-12-16

[5]
LncRNA CCAT2, involving miR-34a/TGF-β1/Smad4 signaling, regulate hepatic stellate cells proliferation.

Sci Rep. 2022-12-8

[6]
CD44 promotes angiogenesis in myocardial infarction through regulating plasma exosome uptake and further enhancing FGFR2 signaling transduction.

Mol Med. 2022-12-3

[7]
Role of extracellular vesicles in cancer-specific interactions between tumour cells and the vasculature.

Semin Cancer Biol. 2022-12

[8]
Exosome biogenesis: machinery, regulation, and therapeutic implications in cancer.

Mol Cancer. 2022-11-1

[9]
Extracellular vesicles as central regulators of blood vessel function in cancer.

Sci Signal. 2022-9-27

[10]
Tumor vessel co-option: The past & the future.

Front Oncol. 2022-8-31

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