The significance of high expression of circulating miR-222-3p in patients with unilateral primary aldosteronism.

原发性醛固酮增多症 表达式(计算机科学) 小学(天文学) 医学 内科学 醛固酮 内分泌学 计算机科学 物理 天文 程序设计语言
作者
Kentaro Okamoto,Masakatsu Sone,Daisuke Taura,Youichi Ohno,Ichiro Yamauchi,Yohei Ueda,Takuro Hakata,Mika Tsuiki,Masanori Murakami,Daisuke Yabe,Nobuya Inagaki,Mitsuhide Naruse
出处
期刊:PubMed [National Institutes of Health]
标识
DOI:10.1210/clinem/dgaf408
摘要

The significance of circulating miRNAs in primary aldosteronism (PA) is still largely unknown. We compared the profiles of circulating miRNAs between unilateral primary aldosteronism (UPA) and bilateral hyperaldosteronism (BHA) and investigated the potential role of a newly identified UPA-related miRNA in the pathogenesis of PA. We initially conducted a comprehensive expression analysis of circulating miRNAs using a qPCR panel in a small number of cases matched for background factors, followed by validation analysis with a larger sample size for the candidate miRNAs. The expression level of one single miRNA, miR-222-3p, was significantly higher in UPA than in BHA, both in the adrenal veins and the inferior vena cava. Moreover, it was significantly higher in the adrenal vein on the tumor side compared to the non-tumor side within the same UPA patients. In primary cultured adrenal cells, miR-222-3p mimics appeared to increase CYP11B2 expression, although the effect was not statistically significant. However, transfection with miR-222-3p mimics significantly increased cell proliferation, while transfection with miR-222-3p inhibitors decreased it. CDKN1B was identified as a predicted target gene of miR-222-3p. Additionally, the expression level of miR-222-3p exhibited a significant positive correlation with tumor diameter and plasma aldosterone concentration after saline infusion test. The present results demonstrated higher expression of circulating miR-222-3p in UPA than in BHA, providing a biochemical marker for subtype diagnosis of PA. Moreover, the correlation of miR-222-3p with adrenal cell proliferation and aldosterone secretion indicated its significant involvement in the pathogenesis of PA.
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