小桶
转移
基因
骨肉瘤
医学
基因本体论
计算生物学
机制(生物学)
基因表达
基因组
生物信息学
癌症
癌症研究
生物
遗传学
内科学
哲学
认识论
作者
Honglai Tian,Dong-Hui Guan,Jianmin Li
出处
期刊:Medicine
[Wolters Kluwer]
日期:2018-06-01
卷期号:97 (24): e10781-e10781
被引量:50
标识
DOI:10.1097/md.0000000000010781
摘要
Osteosarcoma (OS), the most common malignant bone tumor, accounts for the heavy healthy threat in the period of children and adolescents. OS occurrence usually correlates with early metastasis and high death rate. This study aimed to better understand the mechanism of OS metastasis.Based on Gene Expression Omnibus (GEO) database, we downloaded 4 expression profile data sets associated with OS metastasis, and selected differential expressed genes. Weighted gene co-expression network analysis (WGCNA) approach allowed us to investigate the most OS metastasis-correlated module. Gene Ontology functional and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were used to give annotation of selected OS metastasis-associated genes.We select 897 differential expressed genes from OS metastasis and OS non-metastasis groups. Based on these selected genes, WGCNA further explored 142 genes included in the most OS metastasis-correlated module. Gene Ontology functional and KEGG pathway enrichment analyses showed that significantly OS metastasis-associated genes were involved in pathway correlated with insulin-like growth factor binding.Our research figured out several potential molecules participating in metastasis process and factors acting as biomarker. With this study, we could better explore the mechanism of OS metastasis and further discover more therapy targets.
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