Affiliation:
1. Department of Toxicology, College of Public Health, Zhengzhou University, 100 Kexue Avenue, Zhengzhou, Henan Province 450001, China
2. Department of Bone and Soft Tissue Cancer, The Affiliated Cancer Hospital of Zhengzhou University (Henan Cancer Hospital), Zhengzhou, Henan Province 450008, China
Abstract
Background:
Osteosarcoma is one of the most serious primary malignant bone tumors
that threaten the lives of children and adolescents. However, the mechanism underlying and how to
prevent or treat the disease have not been well understood.
Aims & Objective:
This aim of the present study was to identify the key genes and explore novel
insights into the molecular mechanism of miR-542-3p over-expressed Osteosarcoma.
Materials & Methods:
Gene expression profile data GDS5367 was downloaded from the Gene
Expression Omnibus (GEO) database. The differentially expressed genes (DEGs) were screened
using GEO2R, and Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG)
analyses were performed using the DAVID database. And protein-protein interaction (PPI)
network was constructed by the STRING database. In addition, the most highly connected module
was screened by plugin MCODE and hub genes by plugin CytoHubba. Furthermore, UALCAN
and The Cancer Genome Atlas were performed for survival analysis.
Result:
In total, 1421 DEGs were identified, including 598 genes were up-regulated and 823 genes
were down-regulated. GO analysis showed that DEGs were classified into three groups and DEGs
mainly enriched in Steroid biosynthesis, Ubiquitin mediated proteolysis and p53 signaling
pathway. Six hub genes (UBA52, RNF114, UBE2H, TRIP12, HNRNPC, and PTBP1) may be key
genes with the progression of osteosarcoma.
Conclusion:
The results could better understand the mechanism of osteosarcoma, which may
facilitate a novel insight into treatment targets.
Funder
National Natural Science Foundation of China
Publisher
Bentham Science Publishers Ltd.
Subject
Organic Chemistry,Computer Science Applications,Drug Discovery,General Medicine
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献