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ECRG4异常表达与心房颤动之间的潜在联系。

A potential link between aberrant expression of ECRG4 and atrial fibrillation.

作者信息

Zhang Zuojing, Wang Wei, Zhang Yuxin, You Xingji, Wu Jingxiang

机构信息

Department of Anesthesiology, Shanghai Chest Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.

School of Medicine, Shanghai University, Shanghai, China.

出版信息

Front Oncol. 2023 Feb 22;13:1031128. doi: 10.3389/fonc.2023.1031128. eCollection 2023.

DOI:10.3389/fonc.2023.1031128
PMID:36910669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9992723/
Abstract

Esophageal cancer-related gene-4 (ECRG4), a 148-amino acid propertied and new tumor suppressor, is initially cloned from the normal esophageal epithelium. ECRG4 was found to be expressed not only in esophageal tissues but also in cardiomyocytes. Previous studies demonstrated that ECRG4 is constitutively expressed in esophageal epithelial cells, and its degree of downregulation is directly proportional to prognosis in patients with esophageal cancer. In the heart, ECRG4 shows greater expression in the atria than in the ventricles, which accounts for its heterogeneity. Downregulation of ECRG4 expression level correlates with esophageal cancer, as well as myocardial injuries and arrhythmias. As a result, this review summarizes the possible susceptibility gene, ECRG4 and its associated molecular mechanisms in cancer patients with atrial fibrillation and myocardial injury. The review begins by describing ECRG4's biological background, discusses its expression in the cardiovascular system, lists the clinical and animal research related to the downregulation of ECRG4 in atrial fibrillation, and focuses on its potential role in atrial fibrillation. Downregulation of ECRG4 may increase the risk of atrial fibrillation by affecting ion channels, MMPs expression and inflammatory response. We will then discuss how ECRG4 can be used in the treatment of tumors and arrhythmias, and provide a novel possible strategy to reduce the occurrence of perioperative cardiovascular adverse events in patients with tumors such as esophageal cancer and gastric cancer.

摘要

食管癌相关基因4(ECRG4)是一种含148个氨基酸的特性新肿瘤抑制因子,最初从正常食管上皮中克隆得到。研究发现ECRG4不仅在食管组织中表达,在心肌细胞中也有表达。既往研究表明,ECRG4在食管上皮细胞中呈组成性表达,其下调程度与食管癌患者的预后直接相关。在心脏中,ECRG4在心房中的表达高于心室,这解释了其异质性。ECRG4表达水平的下调与食管癌以及心肌损伤和心律失常相关。因此,本综述总结了可能的易感基因ECRG4及其在房颤和心肌损伤癌症患者中的相关分子机制。综述首先描述了ECRG4的生物学背景,讨论了其在心血管系统中的表达,列出了与房颤中ECRG4下调相关的临床和动物研究,并重点关注其在房颤中的潜在作用。ECRG4的下调可能通过影响离子通道、基质金属蛋白酶表达和炎症反应增加房颤风险。然后我们将讨论ECRG4如何用于肿瘤和心律失常的治疗,并提供一种新的可能策略,以减少食管癌和胃癌等肿瘤患者围手术期心血管不良事件的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/9f8dab885bfb/fonc-13-1031128-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/de1477c6b3c3/fonc-13-1031128-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/3f79de83991f/fonc-13-1031128-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/9f8dab885bfb/fonc-13-1031128-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/de1477c6b3c3/fonc-13-1031128-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/3f79de83991f/fonc-13-1031128-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1a/9992723/9f8dab885bfb/fonc-13-1031128-g003.jpg

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[The importance of matrix metalloproteinases in the development of atrial fibrillation in obesity].[基质金属蛋白酶在肥胖患者心房颤动发生发展中的重要性]
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C2orf40 inhibits metastasis and regulates chemo-resistance and radio-resistance of nasopharyngeal carcinoma cells by influencing cell cycle and activating the PI3K/AKT/mTOR signaling pathway.C2orf40 通过影响细胞周期和激活 PI3K/AKT/mTOR 信号通路抑制鼻咽癌细胞的转移并调节其化疗耐药性和放射抵抗性。
J Transl Med. 2022 Jun 8;20(1):264. doi: 10.1186/s12967-022-03446-z.
3
acts as a tumor suppressor in nasopharyngeal carcinoma by suppressing the AKT/GSK3β/β-catenin signaling pathway.
通过抑制AKT/GSK3β/β-连环蛋白信号通路,在鼻咽癌中发挥肿瘤抑制作用。
Cytotechnology. 2022 Apr;74(2):231-243. doi: 10.1007/s10616-022-00520-8. Epub 2022 Jan 27.
4
The effects of paravertebral blockade usage on pulmonary complications, atrial fibrillation and length of hospital stay following thoracoscopic lung cancer surgery.椎旁阻滞在胸腔镜肺癌手术后对肺部并发症、心房颤动及住院时间的影响。
J Clin Anesth. 2022 Aug;79:110770. doi: 10.1016/j.jclinane.2022.110770. Epub 2022 Mar 22.
5
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Clin Res Hepatol Gastroenterol. 2022 May;46(5):101891. doi: 10.1016/j.clinre.2022.101891. Epub 2022 Feb 19.
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