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A novel risk score model based on eight genes and a nomogram for predicting overall survival of patients with osteosarcoma.


ABSTRACT: BACKGROUND:This study aims to identify a predictive model to predict survival outcomes of osteosarcoma (OS) patients. METHODS:A RNA sequencing dataset (the training set) and a microarray dataset (the validation set) were obtained from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) database, respectively. Differentially expressed genes (DEGs) between metastatic and non-metastatic OS samples were identified in training set. Prognosis-related DEGs were screened and optimized by support vector machine (SVM) recursive feature elimination. A SVM classifier was built to classify metastatic and non-metastatic OS samples. Independent prognosic genes were extracted by multivariate regression analysis to build a risk score model followed by performance evaluation in two datasets by Kaplan-Meier (KM) analysis. Independent clinical prognostic indicators were identified followed by nomogram analysis. Finally, functional analyses of survival-related genes were conducted. RESULT:Totally, 345 DEGs and 45 prognosis-related genes were screened. A SVM classifier could distinguish metastatic and non-metastatic OS samples. An eight-gene signature was an independent prognostic marker and used for constructing a risk score model. The risk score model could separate OS samples into high and low risk groups in two datasets (training set: log-rank p?

SUBMITTER: Wu G 

PROVIDER: S-EPMC7245838 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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A novel risk score model based on eight genes and a nomogram for predicting overall survival of patients with osteosarcoma.

Wu Guangzhi G   Zhang Minglei M  

BMC cancer 20200524 1


<h4>Background</h4>This study aims to identify a predictive model to predict survival outcomes of osteosarcoma (OS) patients.<h4>Methods</h4>A RNA sequencing dataset (the training set) and a microarray dataset (the validation set) were obtained from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) database, respectively. Differentially expressed genes (DEGs) between metastatic and non-metastatic OS samples were identified in training set. Prognosis-related DEGs were screened and  ...[more]

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