Tang Xiaolin, Bai Yinshan, Zhang Zhiming, Lu Jianlin
Department of Medical Science, Shunde Polytechnic, Foshan, Guangdong 528300, P.R. China.
Life Science and Engineering College, Foshan University, Foshan, Guangdong 528231, P.R. China.
Exp Ther Med. 2020 Sep;20(3):2209-2217. doi: 10.3892/etm.2020.8928. Epub 2020 Jun 24.
The aim of the present study was to develop a circulating microRNA expression signature for early prediction of osteoporotic fractures and to validate the results using Gene Expression Omnibus (GEO) datasets. The GSE70318 dataset was downloaded from GEO and used to build an osteoporotic fracture prediction model based on the receiver operating characteristic curve and support vector machine (SVM) classification index. The GSE74209 dataset was used as a validation dataset. Additionally, , alkaline phosphatase (ALP) activity was measured in the presence or absence of microRNA (miRNA/miR) treatments in human osteoblast cells. The expression of two selected genes was detected by western blotting. miR-188-3p, miR-942-3p, miR-576-3p and miR-135a-5p were differentially expressed between controls and osteoporotic patients with fractures. SVM classification using these four miRNAs provided better dichotomization. It was further confirmed that miR-576-3p and 135a-5p in the GSE74209 dataset could also significantly discriminate between the controls and fracture patients, the area under the curve of SVM2 was 0.9722 with 95% CI 0.8885-1.056. Further analysis indicated that the target genes of the two miRNAs participated in the Wingless-related integration site, Hedgehog and transforming growth factor-β signaling pathways and osteoclast differentiation. miR-576-3p and miR-135-5p transfection decreased ALP activity and ALP activity was increased in the presence of blocking antisense oligonucleotides. Western blotting indicated miR-576-3p and miR-135-5p decreased CSNK1A1L and LRP6 levels, respectively. In conclusion, two miRNA signatures were developed and validated for the prediction of osteoporotic fractures.
本研究的目的是开发一种循环微RNA表达特征,用于早期预测骨质疏松性骨折,并使用基因表达综合数据库(GEO)数据集验证结果。从GEO下载GSE70318数据集,并用于基于受试者工作特征曲线和支持向量机(SVM)分类指数构建骨质疏松性骨折预测模型。GSE74209数据集用作验证数据集。此外,在人成骨细胞中存在或不存在微RNA(miRNA/miR)处理的情况下测量碱性磷酸酶(ALP)活性。通过蛋白质印迹法检测两个选定基因的表达。miR-188-3p、miR-942-3p、miR-576-3p和miR-135a-5p在对照组和骨折的骨质疏松症患者之间差异表达。使用这四种miRNA进行SVM分类可提供更好的二分法。进一步证实,GSE74209数据集中的miR-576-3p和135a-5p也可显著区分对照组和骨折患者,SVM2曲线下面积为0.9722,95%置信区间为0.8885-1.056。进一步分析表明,这两种miRNA的靶基因参与无翅相关整合位点、刺猬和转化生长因子-β信号通路以及破骨细胞分化。miR-576-3p和miR-135-5p转染降低了ALP活性,而在存在封闭反义寡核苷酸的情况下ALP活性增加。蛋白质印迹法表明,miR-576-3p和miR-135-5p分别降低了CSNK1A1L和LRP6水平。总之,开发并验证了两种用于预测骨质疏松性骨折的miRNA特征。