A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation

Abstract Epidemiological studies have shown a strong correlation between tumor and AF. However, the molecular link between tumor and AF remains unknown. ECRG4, a tumor suppressor gene that is expressed in the A-V node and in sporadic ventricular myocytes, inhibits tumorigenesis and monitors tissue h...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Li Huang, Hua Yu, Xinrong Fan, Xue Li, Liang Mao, Jun Cheng, Xiaorong Zeng, Xitong Dang
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2017
Materias:
R
Q
Acceso en línea:https://doaj.org/article/2b8e3b7feb23479db72e32101f22a330
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:2b8e3b7feb23479db72e32101f22a330
record_format dspace
spelling oai:doaj.org-article:2b8e3b7feb23479db72e32101f22a3302021-12-02T15:05:03ZA Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation10.1038/s41598-017-02902-x2045-2322https://doaj.org/article/2b8e3b7feb23479db72e32101f22a3302017-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-02902-xhttps://doaj.org/toc/2045-2322Abstract Epidemiological studies have shown a strong correlation between tumor and AF. However, the molecular link between tumor and AF remains unknown. ECRG4, a tumor suppressor gene that is expressed in the A-V node and in sporadic ventricular myocytes, inhibits tumorigenesis and monitors tissue homeostasis by functioning as a ‘sentinel’ molecule gauging inflammatory and cell proliferative responses. To explore the potential physiological function of Ecrg4 in heart, we evaluated its distribution in heart, analyzed its expression in patients with persistent AF and in a canine AF model, and dissected the molecular events downstream of Ecrg4. The results showed that the level of Ecrg4 expression is homogenously high in atria and the conduction systems and in sporadic ventricular myocytes. Importantly, the expression of Ecrg4 was significantly decreased in atrial appendages of AF patients than patients with SR. Moreover, in rapid pacing canine AF models, the expression of ECRG4 in atria was significantly decreased compared to that of the controls. Mechanistically, knockdown ECRG4 in atrial myocytes significantly shortened the APDs, inhibited the expression of Gja1, and activated pro-inflammatory cascades and genes involved in cardiac remodeling. These results suggest that Ecrg4 may play a critical role in the pathogenesis of AF.Li HuangHua YuXinrong FanXue LiLiang MaoJun ChengXiaorong ZengXitong DangNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Li Huang
Hua Yu
Xinrong Fan
Xue Li
Liang Mao
Jun Cheng
Xiaorong Zeng
Xitong Dang
A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation
description Abstract Epidemiological studies have shown a strong correlation between tumor and AF. However, the molecular link between tumor and AF remains unknown. ECRG4, a tumor suppressor gene that is expressed in the A-V node and in sporadic ventricular myocytes, inhibits tumorigenesis and monitors tissue homeostasis by functioning as a ‘sentinel’ molecule gauging inflammatory and cell proliferative responses. To explore the potential physiological function of Ecrg4 in heart, we evaluated its distribution in heart, analyzed its expression in patients with persistent AF and in a canine AF model, and dissected the molecular events downstream of Ecrg4. The results showed that the level of Ecrg4 expression is homogenously high in atria and the conduction systems and in sporadic ventricular myocytes. Importantly, the expression of Ecrg4 was significantly decreased in atrial appendages of AF patients than patients with SR. Moreover, in rapid pacing canine AF models, the expression of ECRG4 in atria was significantly decreased compared to that of the controls. Mechanistically, knockdown ECRG4 in atrial myocytes significantly shortened the APDs, inhibited the expression of Gja1, and activated pro-inflammatory cascades and genes involved in cardiac remodeling. These results suggest that Ecrg4 may play a critical role in the pathogenesis of AF.
format article
author Li Huang
Hua Yu
Xinrong Fan
Xue Li
Liang Mao
Jun Cheng
Xiaorong Zeng
Xitong Dang
author_facet Li Huang
Hua Yu
Xinrong Fan
Xue Li
Liang Mao
Jun Cheng
Xiaorong Zeng
Xitong Dang
author_sort Li Huang
title A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation
title_short A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation
title_full A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation
title_fullStr A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation
title_full_unstemmed A Potential Role of Esophageal Cancer Related Gene-4 for Atrial Fibrillation
title_sort potential role of esophageal cancer related gene-4 for atrial fibrillation
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/2b8e3b7feb23479db72e32101f22a330
work_keys_str_mv AT lihuang apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT huayu apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xinrongfan apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xueli apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT liangmao apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT juncheng apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xiaorongzeng apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xitongdang apotentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT lihuang potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT huayu potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xinrongfan potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xueli potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT liangmao potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT juncheng potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xiaorongzeng potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
AT xitongdang potentialroleofesophagealcancerrelatedgene4foratrialfibrillation
_version_ 1718388944235659264