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MiR-16-5p regulates postmenopausal osteoporosis by directly targeting VEGFA

Tao Yu, Xiaomeng You, Haichao Zhou, Wenbao He, Zihua Li, Bing Li, Jiang Xia, Hui Zhu, Youguang Zhao, Guangrong Yu, Yuan Xiong, Yunfeng Yang

2020Aging61 citationsDOIOpen Access PDF

Abstract

were the top three hub genes with the highest degree of betweenness and closeness centrality. TargetScanHuman and DIANA software analyses and dual luciferase reporter assays confirmed that miR-16a-5p directly targets the 3'UTR of VEGFA. Postmenopausal patients with osteoporosis showed higher miR-16-5p and lower VEGFA levels than those without osteoporosis (n=10 each). VEGFA levels were higher in miR-16-5p knockdown hMSCs and were reduced in miR-16-5p-overexpressing hMSCs. mRNA expression of osteogenic markers, ALP, OCN, and RUNX2, as well as calcium deposition based on Alizarin red staining, correlated inversely with miR-16-5p levels and correlated positively with VEGFA levels. These findings suggest that miR-16-5p suppresses osteogenesis by inhibiting VEGFA expression and is a promising target for postmenopausal osteoporosis therapy.

Topics & Concepts

Vascular endothelial growth factor ARUNX2OsteoporosisGene knockdownmicroRNAMesenchymal stem cellDownregulation and upregulationCancer researchOsteopontinBiologyMedicineEndocrinologyVascular endothelial growth factorCell biologyVEGF receptorsGene expressionGeneGeneticsBone Metabolism and DiseasesMicroRNA in disease regulationCircular RNAs in diseases
MiR-16-5p regulates postmenopausal osteoporosis by directly targeting VEGFA | Litcius