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. 2024 Jul 17;13(7):3217–3241. doi: 10.21037/tcr-23-2332

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2024 Translational Cancer Research. All rights reserved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0.

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The expression of classical markers and risk model genes across different subsets in scRNA-seq GSE176021 dataset. (A) The expression of some classical markers on dotplot across different cell subsets. (B) The expression of some classical markers on violin plots across different cell subsets. (C) The metabolic status of different clusters of cell types. (D) The expression levels of the genes selected for risk model on dotplot. (E) The expression levels of the genes selected for risk model on violin plot. DC, dendritic cell; Tprolif, proliferating T cell; NK, natural killer; CD8Tex, exhausted CD8⁺ T cell; CD8T, CD8⁺ T cell; Treg, regulatory T cell; CD4Tconv, conventional CD4⁺ T cells; scRNA-seq, single-cell RNA-sequencing.