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©The Author(s) 2024.
World J Gastrointest Oncol. May 15, 2024; 16(5): 1908-1924
Published online May 15, 2024. doi: 10.4251/wjgo.v16.i5.1908
Published online May 15, 2024. doi: 10.4251/wjgo.v16.i5.1908
Figure 5 Analysis of tumor microenvironments and response to immunotherapy among patients with high- and low-risk centrosome-related signature.
A: The fraction of 22 CIBERSORT immune cell types in high- and low-risk subgroups; B: The correlation between each signature gene and 16 immune cell types using CIBERSORT; C-E: The correlation between the risk score of centrosome-related signature (CRS) and immune cell types using CIBERSORT; F: Comparison of the tumor microenvironment scores between high- and low-risk CRS using ESTIMATE. Stromal score and estimate score were significantly higher in the high-risk CRS group than in the low-risk CRS group (P < 0.01 and P < 0.05, respectively). No significant difference was found between these two groups for the immune score; G and H: Tumor immune dysfunction and exclusion algorithm showed patients with a high-risk signature were insensitive to immunotherapy. aP < 0.05. bP < 0.01. cP < 0.001 vs high-risk and low-risk groups.
- Citation: Wang HY, Diao Y, Tan PZ, Liang H. Four centrosome-related genes to predict the prognosis and drug sensitivity of patients with colon cancer. World J Gastrointest Oncol 2024; 16(5): 1908-1924
- URL: https://www.wjgnet.com/1948-5204/full/v16/i5/1908.htm
- DOI: https://dx.doi.org/10.4251/wjgo.v16.i5.1908