In conclusion, the highly significant differences between the tumor immune microenvironment and the type of immune cell infiltration in patients in the high/low risk group, which correlated with RS and could have a significant impact on patient prognosis, demonstrated that the oxidative stress-related risk subgroups are probably with different tumor immune response patterns and may have a higher benefit when adopting different immunotherapy strategies during clinical treatment.
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Comprehensive analysis of oxidative stress-related lncRNA signatures in glioma reveals the discrepancy of prognostic and immune infiltration.
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S8 B,F, S9 A,D), this difference may be indicative of variations of gene expression patterns in glioma patients from different countries and regions, almost all the above analyses showed a trend consistent with the results of the TCGA dataset analysis.