Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/32288
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18056/20254 (89%)
Visitors : 650620      Online Users : 557
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/32288


    Title: MicroRNA-21 is Associated with the Severity of Right Ventricular Dysfunction in Patients with Hypoxia-Induced Pulmonary Hypertension
    Authors: Chang, Wei-Ting
    Hsu, Chih-Hsin
    Huang, Tzu-Ling
    Tsai, Ying-Ching
    Chiang, Chun-Yen
    Chen, Zhih-Cherng
    Shih, Jhih-Yuan
    Contributors: Chi Mei Med Ctr, Dept Internal Med, Div Cardiol
    Southern Taiwan Univ Sci & Technol, Dept Biotechnol
    Cheng Kung Univ Hosp, Dept Intens Care Med
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Keywords: Hypoxia-induced pulmonary hypertension
    miR-21
    Right ventricular dysfunction
    Date: 2018-11
    Issue Date: 2019-11-15 15:48:14 (UTC+8)
    Publisher: TAIWAN SOC CARDIOLOGY
    Abstract: Background: The outcome of pulmonary hypertension (PH) mainly depends on the development of right ventricular (RV) dysfunction, and survival among patients with different etiologies of PH varies. Chronic hypoxia is a major cause of secondary PH, however the mechanisms of its associated RV dysfunction are largely unknown. Herein, we studied the role of microRNA-21 (miR-21) in hypoxia-induced RV dysfunction. Methods: In this longitudinal, prospective study, we enrolled 41 patients with hypoxia-induced PH. Echocardiography was conducted and circulating miR-21 was measured. The expression of miR-21 was also evaluated in hypoxiatreated human pulmonary microvascular endothelial cells (HPECs) and conditioned media. Through the over expression of miR-21 in H9C2 cells, we further identified crosstalk between the pulmonary circulation and RV. Results: Among the studied patients, 10 developed RV dysfunction. Notably, the expression of circulating miR-21 was correlated with the severity of RV dysfunction. Likewise, miR-21 was up-regulated in the hypoxia-treated HPECs and its conditioned media in a time-dependent manner. I addition, hypertrophic changes were observed in the hypoxia-treated HPECs. The up-regulation of heart failure-associated markers in H9C2 cells over-expressing miR-21 implied the influence of pulmonary circulatory miR-21 on RV function. Conclusions: The expression of systemic and pulmonary miR-21 is associated with the severity of RV dysfunction in patients with hypoxia-induced PH.
    ???metadata.dc.relation.uri???: http://dx.doi.org/10.6515/ACS.201811_34(6).20180613A
    Relation: Journal of Microbiology Immunology and Infection, v.34, n.6, pp.511-517
    Appears in Collections:[Dept. of Pharmacy] Periodical Articles

    Files in This Item:

    File Description SizeFormat
    10.6515-ACS.201811_34(6).20180613A.pdf362KbAdobe PDF416View/Open
    index.html0KbHTML1567View/Open


    All items in CNU IR are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback