Research Paper Volume 15, Issue 13 pp 6264—6291

Identification of natural killer cell-related characteristics to predict the clinical prognosis and immune microenvironment of patients with low-grade glioma

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Figure 8. Immunological characteristics and drug sensitivities between different RiskScore groups. (A) The difference in “T cell inflamed GEP score” among various molecular subtypes. (B) The difference in “response to IFN-γ” among various molecular subtypes. (C) The difference in “Cytolytic activity” among various molecular subtypes. (D) Expression differences of immune checkpoint-associated genes among various molecular subtypes. (E) A box plot of the estimated IC50 values for temozolomide, bleomycin, cisplatin, cyclopamine, A-443654, AZD6482, and GDC0941 in TCGA-LGG. **P < 0.01; ****P < 0.0001. Abbreviations: ns: no significance; GEP: gene expression profile; IFN: interferon; TPM: transcripts per million; IC50: half-maximal inhibitory concentration; TCGA: The Cancer Genome Atlas; LGG: low-grade glioma.