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pmid:31333788

Co-Expression Network Analysis Identified Gene Signatures in Osteosarcoma as a Predictive Tool for Lung Metastasis and Survival.

Honghua Zhang · Linwei Guo · Zheng Zhang · Yunlong Sun · Honglei Kang · Chao Song · Huiyong Liu · Zhuowei Lei · Jia Wang · Baoguo Mi · Qian Xu · Hanfeng Guan · Feng Li

Journal of Cancer · 2019 doi:10.7150/jca.32092

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:31333788
kind
science-record
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2026-11-01T15:40:47Z
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2026-11-01T22:00:43Z
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paper object · 10 fields
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title
Co-Expression Network Analysis Identified Gene Signatures in Osteosarcoma as a Predictive Tool for Lung Metastasis and Survival.
doi
10.7150/jca.32092
pmid
31333788
authors array · 13 items
[0]
Honghua Zhang
[1]
Linwei Guo
[2]
Zheng Zhang
[3]
Yunlong Sun
[4]
Honglei Kang
[5]
Chao Song
[6]
Huiyong Liu
[7]
Zhuowei Lei
[8]
Jia Wang
[9]
Baoguo Mi
[10]
Qian Xu
[11]
Hanfeng Guan
[12]
Feng Li
journal
Journal of Cancer
year
2019
abstract
Osteosarcoma (OS) is the most common primary bone tumor, whose poor prognosis is mainly due to lung metastasis. The aim of this study is to build a practical and valid diagnostic test that can predict the risk of OS metastasis and progression. We performed weighted gene co-expression network analysis (WGCNA) on GSE21257 from the Gene Expression Omnibus (GEO) database, which contains microarray data of biopsies from OS patients. In these modules, the highest association was found between the blue module and metastasis stage (r = -0.52) by Pearson's correlation analysis. Based on Least Absolute Shrinkage and Selection Operator (LASSO) Cox regression, we derived eight clinically significant genes and constructed an eight-gene signature for metastasis status. It showed great efficacy to distinguish metastasis from non-metastasis (AUC = 0.886) and the results were validated in The Cancer Genome Atlas (TCGA) database. Functional enrichment analysis of hub genes showed that their biological processes focused on immune-related pathways, suggesting the important roles of immune cells, immune pathways and the tumor microenvironment in metastasis development. In conclusion, we discovered an efficient gene signature with great efficacy to distinguish metastasis status, which may help improve early diagnosis and treatment, enhancing the clinical outcomes of OS patients. Besides we created an effective protocol to seek for several hub genes in high-throughput data by combining WGCNA and LASSO Cox regression.
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In the current study, WGCNA was performed on DEG-matched GSE21257, and modules were identified with a dynamic tree-cutting algorithm with a minimum module size of 10 genes, a scale-free topology threshold of 0.9 and merged with a MEDissThres parameter of 0.25.
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sections[5] "Constructing Dynamic Weighted Gene Co-Expression Network" paragraph 3
quote
In the current study, WGCNA was performed on DEG-matched GSE21257, and modules were identified with a dynamic tree-cutting algorithm with a minimum module size of 10 genes, a scale-free topology threshold of 0.9 and merged with a MEDissThres parameter of 0.25.
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sections[3] "Data Sources and Data Preprocessing" paragraph 2
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Genome-wide gene expression profiling on pre-chemotherapy biopsies of osteosarcoma patients who developed metastases within 5yrs (n=34) and patients who did not develop metastases within 5yrs (n=19)
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Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma [gene expression]
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Genome-wide gene expression profiling of mesenchymal stem cells, osteosarcoma cells, and osteosarcoma cell lines.
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Complete file
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