Screening for Key Pathways Associated with the Development of Osteoporosis by Bioinformatics Analysis.

Objectives. We aimed to find the key pathways associated with the development of osteoporosis. Methods. We downloaded expression profile data of GSE35959 and analyzed the differentially expressed genes (DEGs) in 3 comparison groups (old_op versus middle, old_op versus old, and old_op versus senescen...

Descripción completa

Detalles Bibliográficos
Publicado en:BioMed Research International Vol. 2017; pp. 1 - 9
Autores principales: Liu, Yanqing, Wang, Yueqiu, Zhang, Yanxia, Liu, Zhiyong, Xiang, Hongfei, Peng, Xianbo, Chen, Bohua, Jia, Guyou
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell 3/30/2017
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Objectives. We aimed to find the key pathways associated with the development of osteoporosis. Methods. We downloaded expression profile data of GSE35959 and analyzed the differentially expressed genes (DEGs) in 3 comparison groups (old_op versus middle, old_op versus old, and old_op versus senescent). KEGG (Kyoto Encyclopedia of Genes and Genomes) pathway enrichment analyses were carried out. Besides, Venn diagram analysis and gene functional interaction (FI) network analysis were performed. Results. Totally 520 DEGs, 966 DEGs, and 709 DEGs were obtained in old_op versus middle, old_op versus old, and old_op versus senescent groups, respectively. Lysosome pathway was the significantly enriched pathways enriched by intersection genes. The pathways enriched by subnetwork modules suggested that mitotic metaphase and anaphase and signaling by Rho GTPases in module 1 had more proteins from module. Conclusions. Lysosome pathway, mitotic metaphase and anaphase, and signaling by Rho GTPases may be involved in the development of osteoporosis. Furthermore, Rho GTPases may regulate the balance of bone resorption and bone formation via controlling osteoclast and osteoblast. These 3 pathways may be regarded as the treatment targets for osteoporosis.