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. 2022 Jul 5;24(3):301. doi: 10.3892/ol.2022.13421

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Copyright: © Wang et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 7. — Single-sample gene set enrichment analysis results of different risk groups in the (A and B) The Cancer Genome Atlas cohort: (A) Scores of the 16 immune cells and (B) 13 immune-related functions. (C and D) Gene Expression Omnibus cohort: (C) Scores of the 16 immune cells and (D) 13 immune-related functions. ns, not significant; *P<0.05; **P<0.01; ***P<0.001. DC, dendritic cells; NK, natural killer; Tfh, follicular helper T cells; Th1, type I T-helper cells; TIL, tumor-infiltrating lymphocytes; Treg, regulatory T cells; HLA, human leukocyte antigen; APC, antigen-presenting cell; MHC, major histocompatibility complex; CCR, chemokine receptors; pDCs, plasmacytoid DCs; aDCs, activated DCs; iDCs, immature DCs.