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pmid:36033493
Construction of a solid Cox model for AML patients based on multiomics bioinformatic analysis.
Fu Li · Jiao Cai · Jia Liu · Shi-Cang Yu · Xi Zhang · Yi Su · Lei Gao
Frontiers in oncology · 2022 doi:10.3389/fonc.2022.925615
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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In this study, we aimed to identify reliable immune-related biomarkers for AML prognosis by multiomics analysis. We obtained expression profiles from The Cancer Genome Atlas (TCGA) database and constructed a LASSO-Cox regression model to predict the prognosis of AML using multiomics bioinformatic analysis data. This was followed by independent validation of the model in the GSE106291 (n=251) data set and mutated genes in clinical samples for predicting overall survival (OS). Molecular docking was performed to predict the most optimal ligands to the genes in prognostic model. The single-cell RNA sequence dataset GSE116256 was used to clarify the expression of the hub genes in different immune cell types. According to their significant differences in immune gene signatures and survival trends, we concluded that the immune infiltration-lacking subtype (IL type) is associated with better prognosis than the immune infiltration-rich subtype (IR type). 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