Zhou Sijing, Li Min, Zeng Daxiong, Xu Xuan, Fei Liming, Zhu Qingqing, Zhang Yan, Wang Ran
Hefei Prevention and Treatment Center for Occupational Diseases, Hefei, China.
Cell Physiol Biochem. 2015;36(1):166-78. doi: 10.1159/000374061. Epub 2015 Apr 30.
Polymorphisms located at microRNA (miRNA) binding sites may interfere with the miRNA/mRNA interaction. The objective of this study was to identify the association between a single nucleotide polymorphism (774 T>C) in 3'-untranslated region (3'-UTR) of Epithelial Growth Factor Receptor (EGFR) and development of pulmonary hypertension (PH) in chronic obstructive pulmonary disease (COPD) as well as to explore the molecular mechanism.
In this study, we validated EGFR as a target of miR-214 in pulmonary artery smooth muscle cell (PASMC), which was further confirmed by the observation that exogenous overexpression of miR-214 significantly downregulated the expression of EGFR in the PASMCs genotyped as TT or TC, but not in CC group. Meanwhile, we found COPD patients with CC genotype had significantly higher risk for PH (OR = 1.965, p = 0.0095), compared with TT and TC genotypes,. Additionally, the PASMCs were isolated from 72 COPD patients, with which miR-214 and EGFR expression levels were determined, and we found that miR-214 level was comparable between each genotype group, the concentration of EGFR in CC genotype group was significantly higher than in TT or TC genotype group.
Our study confirmed that EGFR 3'UTR 774 T>C polymorphism interfered with miRNA/mRNA interaction, and showed that the minor allele was associated with an elevated risk for development of PH in COPD.
位于微小RNA(miRNA)结合位点的多态性可能会干扰miRNA/信使核糖核酸(mRNA)的相互作用。本研究的目的是确定上皮生长因子受体(EGFR)3'-非翻译区(3'-UTR)的单核苷酸多态性(774 T>C)与慢性阻塞性肺疾病(COPD)患者肺动脉高压(PH)发生之间的关联,并探讨其分子机制。
在本研究中,我们验证了EGFR是肺动脉平滑肌细胞(PASMC)中miR-214的靶点,这一结果通过以下观察进一步得到证实:miR-214的外源性过表达显著下调了基因型为TT或TC的PASMC中EGFR的表达,但在CC组中未下调。同时,我们发现与TT和TC基因型相比,CC基因型的COPD患者发生PH的风险显著更高(比值比[OR]=1.965,p=0.0095)。此外,从72例COPD患者中分离出PASMC,测定了miR-214和EGFR的表达水平,我们发现各基因型组之间miR-214水平相当,CC基因型组中EGFR的浓度显著高于TT或TC基因型组。
我们的研究证实EGFR 3'UTR 774 T>C多态性干扰了miRNA/mRNA的相互作用,并表明次要等位基因与COPD患者发生PH的风险升高有关。