miR-28-5p Involved in LXR-ABCA1 Pathway is Increased in the Plasma of Unstable Angina Patients

Background Previous studies confirmed that the intronic miRNAs participated in regulating host gene-primed biological processes. The coordinated roles of miR-28 with its host gene, LIM domain lipoma-preferred partner (LPP), remain unknown in atherosclerosis. Methods In this study, we determined to a...

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Veröffentlicht in:Heart, lung & circulation lung & circulation, 2015-07, Vol.24 (7), p.724-730
Hauptverfasser: Liu, Jia, Liu, Ying, Sun, Ya-Nan, Li, Si, Liu, Xue-Qing, Li, Jie, Li, Chun-Mei, Tian, Wei, PhD, Zhou, Yun-Tao, PhD, Shang, Xiao-Ming, MD
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Sprache:eng
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Zusammenfassung:Background Previous studies confirmed that the intronic miRNAs participated in regulating host gene-primed biological processes. The coordinated roles of miR-28 with its host gene, LIM domain lipoma-preferred partner (LPP), remain unknown in atherosclerosis. Methods In this study, we determined to assess circulating levels of miR-28-5p in unstable angina patients, compared with age- and sex- matched control subjects by quantitative PCR. Furthermore, we attempted to explore whether miR-28-5p could influence the expression of ATP-binding cassette transporter A1 (ABCA1) and liver X receptor (LXR), major mediators of high density lipoprotein (HDL) synthesis and transportation in hepatic cells and macrophages. Results It was found that plasma levels of miR-28-5p were significantly increased in unstable angina patients with or without type 2 diabetes mellitus. Notably, miR-28-5p upregulated ABCA1 expression at transcription and translation levels, strongly correlated with translational activation of LXRα in HepG2 and THP-1-derived macrophages. Conclusions Our findings suggest that circulating miR-28-5p, involved in LXRα-ABCA1 pathway, may be a potential biomarker for diagnosis and prognosis of unstable angina.
ISSN:1443-9506
1444-2892
DOI:10.1016/j.hlc.2014.12.160