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pmid:35762414
Dissecting the ferroptosis-related prognostic biomarker and immune microenvironment of driver gene-negative lung cancer.
Rui Zhou · Hao-Chuan Ma · Yi-Hong Liu · Xian Chen · Xue-Song Chang · Ya-Dong Chen · Li-Rong Liu · Yong Li · Yan-Juan Zhu · Hai-Bo Zhang
Experimental biology and medicine (Maywood, N.J.) · 2022 doi:10.1177/15353702221102872
Paper
complete
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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Numerous studies have shown that ferroptosis plays an essential role in antitumor activity. To identify the molecular regulation patterns associated with ferroptosis, 351 EGFR/ALKWT NSCLC samples with low-level PD-L1 were extracted from The Cancer Genome Atlas (TCGA) and clustered using the k-means clustering technique. The two clusters associated with ferroptosis showed significantly different prognoses. In total, 169 differential expression genes (DEGs) were identified. Cluster differential analysis revealed that Cluster 1 had a significantly poorer overall survival (OS) and was associated with more negative immune regulation. In addition, TCGA samples were randomly assigned in a 7:3 ratio to a training group or testing group. A signature of eight genes associated with ferroptosis was established in the training cohort using DEGs and validated in the test cohort and three independent cohorts (GSE72049, GSE41271, and GSE50081). 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