Circulating microRNA signature of steroid-induced osteonecrosis of the femoral head

被引:35
|
作者
Li, Zheng [1 ,2 ]
Jiang, Chao [1 ,2 ,3 ]
Li, Xingye [1 ,2 ,4 ]
Wu, William K. K. [5 ,6 ]
Chen, Xi [1 ,2 ]
Zhu, Shibai [1 ,2 ]
Ye, Chanhua [1 ,2 ]
Chan, Matthew T. V. [5 ]
Qian, Wenwei [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Dept Orthopaed Surg, Peking Union Med Coll Hosp, Beijing, Peoples R China
[2] Peking Union Med Coll, Beijing, Peoples R China
[3] Zhejiang Univ, Shaoxing Hosp, Dept Orthopaed, Shaoxing Peoples Hosp, Shaoxing, Peoples R China
[4] Tsinghua Univ, Dept Orthoped Surg, Jishuitan Orthopaed Coll, Beijing Jishuitan Hosp,Clin Coll 4,Peking Univ, Beijing, Peoples R China
[5] Chinese Univ Hong Kong, Dept Anaesthesia & Intens Care, Hong Kong, Hong Kong, Peoples R China
[6] Chinese Univ Hong Kong, Li Ka Shing Inst Hlth Sci, State Key Lab Digest Dis, Hong Kong, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
circulating microRNAs; GO; KEGG; ONFH; osteonecrosis of the femoral head; GENE ONTOLOGY TERMS; NONTRAUMATIC OSTEONECROSIS; CELL-PROLIFERATION; KEGG PATHWAYS; RAT MODEL; EXPRESSION; DIFFERENTIATION; IDENTIFICATION; OSTEOSARCOMA; POPULATION;
D O I
10.1111/cpr.12418
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
ObjectivesSteroid-induced osteonecrosis of the femoral head (ONFH) is a common orthopaedic disease of which early detection remains clinically challenging. Accumulating evidences indicated that circulating microRNAs (miRNAs) plays vital roles in the development of several bone diseases. However, the association between circulating miRNAs and steroid-induced ONFH remains elusive. Materials and methodsmiRNA microarray was performed to identify the differentially abundant miRNAs in the serums of systemic lupus erythematosus (SLE) patients with steroid-induced ONFH as compared with SLE control and healthy control group. We predicted the potential functions of these differentially abundant miRNAs using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses and reconstructed the regulatory networks of miRNA-mRNA interactions. ResultsOur data indicated that there were 11 differentially abundant miRNAs (2 upregulated and 9 downregulated) between SLE-ONFH group and healthy control group and 42 differentially abundant miRNAs (14 upregulated and 28 downregulated) between SLE-ONFH group and SLE control group. We also predicted the potential functions of these differentially abundant miRNAs using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses and reconstructed the regulatory networks of miRNA-mRNA interactions. ConclusionsThese findings corroborated the idea that circulating miRNAs play significant roles in the development of ONFH and may serve as diagnostic markers and therapeutic targets.
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页数:13
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