LINC00528 regulates myocardial infarction by targeting the miR-143-3p/COX-2 axis

被引:48
|
作者
Liu, Ketong [1 ]
Zhao, Di [2 ]
Wang, Di [3 ]
机构
[1] Qiqihar Med Univ, Affiliated Hosp 3, Dept Cardiol 3, Qiqihar, Heilongjiang, Peoples R China
[2] Qiqihar Med Univ, Affiliated Hosp 3, Dept Cardiol 1, Qiqihar, Heilongjiang, Peoples R China
[3] Qiqihar Med Univ, Affiliated Hosp 3, Dept Gastroenterol 1, Qiqihar 161000, Heilongjiang, Peoples R China
关键词
Myocardial infarction; LINC00528; miR-143-3p; COX-2; CIRCULATING MICRORNAS; LNCRNA; RNA; EXPRESSION; COX-2;
D O I
10.1080/21655979.2019.1704535
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This study is aimed to explore the roles of LINC00528 in myocardial infarction (MI) progression. Quantitative real-time PCR showed that the expression of LINC00528 and COX-2 was upregulated while miR-143-3p expression was down-regulated in post-MI cells. In function assays, LINC00528 suppression promoted post-MI cells proliferation and reduced cell apoptosis in vitro. In mechanism, LINC00528 interacted with miR-143-3p in post-MI cells. COX-2 served as a target of miR-143-3p in post-MI cells. Besides, LINC00528 inhibition on COX-2 expression and post-MI cells progression could be partially abolished by miR-143-3p inhibitors. Therefore, our findings suggested that LINC00528 exerted its regulatory roles in MI via the miR-143-3p/COX-2 axis, which provided a potential therapeutic target for MI patients treatment.
引用
收藏
页码:11 / 18
页数:8
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