文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

从DNA修复到氧化还原信号传导:APEX1(脱嘌呤/脱嘧啶核酸内切酶1)在心血管健康与疾病中的多面角色

From DNA Repair to Redox Signaling: The Multifaceted Role of APEX1 (Apurinic/Apyrimidinic Endonuclease 1) in Cardiovascular Health and Disease.

作者信息

Yuan Huan-Huan, Yin Hao, Marincas Mara, Xie Ling-Li, Bu Lan-Lan, Guo Min-Hua, Zheng Xi-Long

机构信息

Key Laboratory of Hunan Province for Integrated Traditional Chinese and Western Medicine on Prevention and Treatment of Cardio-Cerebral Diseases, College of Integrated Traditional Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha 410208, China.

Department of Biochemistry & Molecular Biology, Libin Cardiovascular Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4Z6, Canada.

出版信息

Int J Mol Sci. 2025 Mar 26;26(7):3034. doi: 10.3390/ijms26073034.


DOI:10.3390/ijms26073034
PMID:40243693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11988304/
Abstract

Apurinic/apyrimidinic endonuclease 1 (APEX1) serves as a potent regulatory factor in innate immunity, exhibiting both redox and endonuclease activities. Its redox function enables the regulation of transcription factors such as NF-κB or STAT3, whereas its endonuclease activity recognizes apurinic/apyrimidinic (AP) sites in damaged DNA lesions during base excision repair (BER) and double-stranded DNA repair, thereby I confirm.anti-inflammatory, antioxidative stress and antiapoptotic effects. APEX1 is expressed in a variety of cell types that constitute the cardiovascular system, including cardiomyocytes, endothelial cells, smooth muscle cells, and immune cells. Emerging genetic and experimental evidence points towards the functional roles of APEX1 in the pathophysiology of cardiovascular diseases, including neointimal formation and atherosclerosis. This review aims to present comprehensive coverage of the up-to-date literature concerning the molecular and cellular functions of APEX1, with a particular focus on how APEX1 contributes to the (dys)functions of different cell types during the pathogenesis of cardiovascular diseases. Furthermore, we underscore the potential of APEX1 as a therapeutic target for the treatment of cardiovascular diseases.

摘要

脱嘌呤/脱嘧啶核酸内切酶1(APEX1)在先天免疫中作为一种强效调节因子,兼具氧化还原和核酸内切酶活性。其氧化还原功能能够调节诸如核因子κB(NF-κB)或信号转导和转录激活因子3(STAT3)等转录因子,而其核酸内切酶活性在碱基切除修复(BER)和双链DNA修复过程中识别受损DNA损伤中的脱嘌呤/脱嘧啶(AP)位点,从而发挥抗炎、抗氧化应激和抗凋亡作用。APEX1在构成心血管系统的多种细胞类型中表达,包括心肌细胞、内皮细胞、平滑肌细胞和免疫细胞。新出现的遗传学和实验证据表明APEX1在心血管疾病的病理生理学中具有功能性作用,包括新生内膜形成和动脉粥样硬化。本综述旨在全面涵盖有关APEX1分子和细胞功能的最新文献,特别关注APEX1在心血管疾病发病机制中如何促成不同细胞类型的(功能失调)功能。此外,我们强调APEX1作为心血管疾病治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/72b32a14d8f8/ijms-26-03034-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/3d6f3b5c2310/ijms-26-03034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/6d285e7ec147/ijms-26-03034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/407133257926/ijms-26-03034-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/72b32a14d8f8/ijms-26-03034-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/3d6f3b5c2310/ijms-26-03034-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/6d285e7ec147/ijms-26-03034-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/407133257926/ijms-26-03034-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b78/11988304/72b32a14d8f8/ijms-26-03034-g004.jpg

相似文献

[1]
From DNA Repair to Redox Signaling: The Multifaceted Role of APEX1 (Apurinic/Apyrimidinic Endonuclease 1) in Cardiovascular Health and Disease.

Int J Mol Sci. 2025-3-26

[2]
Mild phenotype of knockouts of the major apurinic/apyrimidinic endonuclease APEX1 in a non-cancer human cell line.

PLoS One. 2021

[3]
The role of the N-terminal domain of human apurinic/apyrimidinic endonuclease 1, APE1, in DNA glycosylase stimulation.

DNA Repair (Amst). 2018-2-11

[4]
Endonuclease and redox activities of human apurinic/apyrimidinic endonuclease 1 have distinctive and essential functions in IgA class switch recombination.

J Biol Chem. 2019-1-31

[5]
Identification of Novel Pathways Regulated by APE1/Ref-1 in Human Retinal Endothelial Cells.

Int J Mol Sci. 2023-1-6

[6]
AP endonuclease 1 (Apex1) influences brain development linking oxidative stress and DNA repair.

Cell Death Dis. 2019-4-25

[7]
S-adenosylmethionine regulates apurinic/apyrimidinic endonuclease 1 stability: implication in hepatocarcinogenesis.

Gastroenterology. 2009-3

[8]
A Novel Hypomorphic Mouse Model Implicates Apurinic/Apyrimidinic Endonuclease 1 in Oxidative DNA Damage Repair in Gastric Epithelial Cells.

Antioxid Redox Signal. 2023-1

[9]
APEX1 in intestinal epithelium triggers neutrophil infiltration and intestinal barrier damage in ulcerative colitis.

Free Radic Biol Med. 2024-11-20

[10]
Inhibitors of nuclease and redox activity of apurinic/apyrimidinic endonuclease 1/redox effector factor 1 (APE1/Ref-1).

Bioorg Med Chem. 2017-5-1

本文引用的文献

[1]
DNA damage response, a double-edged sword for vascular aging.

Ageing Res Rev. 2023-12

[2]
Single-Nucleotide Polymorphisms in Base-Excision Repair-Related Genes Involved in the Risk of an Occurrence of Non-Alcoholic Fatty Liver Disease.

Int J Mol Sci. 2023-7-11

[3]
Revisiting Two Decades of Research Focused on Targeting APE1 for Cancer Therapy: The Pros and Cons.

Cells. 2023-7-20

[4]
Promoters telomeres: AP-endonuclease 1 interactions with abasic sites in G-quadruplex folds depend on topology.

RSC Chem Biol. 2023-1-18

[5]
Incidence of Atherosclerotic Cardiovascular Disease in Young Adults at Low Short-Term But High Long-Term Risk.

J Am Coll Cardiol. 2023-2-21

[6]
Apurinic/apyrimidinic endonuclease 1 regulates palmitic acid-mediated apoptosis in cardiomyocytes via endoplasmic reticulum stress.

Biochem Biophys Res Commun. 2023-4-2

[7]
NEDD4 attenuates oxidized low‑density lipoprotein‑induced inflammation and dysfunction in vascular endothelial cells via regulating APEX1 expression.

Exp Ther Med. 2023-1-4

[8]
Effectiveness of interventions to increase device-measured physical activity in pregnant women: systematic review and meta-analysis of randomised controlled trials.

Int J Behav Nutr Phys Act. 2022-12-1

[9]
Iron overload, oxidative stress and vascular dysfunction: Evidences from clinical studies and animal models.

Biochim Biophys Acta Gen Subj. 2022-9

[10]
Targeting DNA damage response in cardiovascular diseases: from pathophysiology to therapeutic implications.

Cardiovasc Res. 2023-5-2

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索