Identification and validation of a pyroptosis-related prognostic model for colorectal cancer based on bulk and single-cell RNA sequencing data

被引:2
|
作者
Zhu, Li-Hua [1 ]
Yang, Jun [1 ]
Zhang, Yun-Fei [1 ]
Yan, Li [2 ]
Lin, Wan-Rong [3 ]
Liu, Wei-Qing [2 ,4 ]
机构
[1] Kunming Med Univ, Affiliated Hosp 1, Dept Surg Oncol, Kunming 650032, Yunnan, Peoples R China
[2] Kunming Med Univ, Affiliated Hosp 1, Dept Internal Med Oncol, Kunming 650032, Yunnan, Peoples R China
[3] Kunming Med Univ, Affiliated Hosp 1, Dept Oncol, Kunming 650032, Yunnan, Peoples R China
[4] Kunming Med Univ, Affiliated Hosp 1, Dept Internal Med Oncol, 295 Xichang Rd, Kunming 650032, Yunnan, Peoples R China
来源
WORLD JOURNAL OF CLINICAL ONCOLOGY | 2024年 / 15卷 / 02期
基金
中国国家自然科学基金;
关键词
Colorectal cancer; Pyroptosis; Single-cell RNA sequencing; Immune infiltration; Prognostic model; IMMUNE CELLS; PREDICTION; PROTEINS; INFLAMMATION; METASTASIS; EXPRESSION; SIGNATURE;
D O I
10.5306/wjco.v15.i2.329
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND Pyroptosis impacts the development of malignant tumors, yet its role in colorectal cancer (CRC) prognosis remains uncertain. AIM To assess the prognostic significance of pyroptosis-related genes and their association with CRC immune infiltration. METHODS Gene expression data were obtained from The Cancer Genome Atlas (TCGA) and single-cell RNA sequencing dataset GSE178341 from the Gene Expression Omnibus (GEO). Pyroptosis-related gene expression in cell clusters was analyzed, and enrichment analysis was conducted. A pyroptosis-related risk model was developed using the LASSO regression algorithm, with prediction accuracy assessed through K-M and receiver operating characteristic analyses. A nomogram predicting survival was created, and the correlation between the risk model and immune infiltration was analyzed using CIBERSORTx calculations. Finally, the differential expression of the 8 prognostic genes between CRC and normal samples was verified by analyzing TCGA-COADREAD data from the UCSC database. RESULTS An effective pyroptosis-related risk model was constructed using 8 genes-CHMP2B, SDHB, BST2, UBE2D2, GJA1, AIM2, PDCD6IP, and SEZ6L2 (P < 0.05). Seven of these genes exhibited differential expression between CRC and normal samples based on TCGA database analysis (P < 0.05). Patients with higher risk scores demonstrated increased death risk and reduced overall survival (P < 0.05). Significant differences in immune infiltration were observed between low- and high-risk groups, correlating with pyroptosis-related gene expression. CONCLUSION We developed a pyroptosis-related prognostic model for CRC, affirming its correlation with immune infiltration. This model may prove useful for CRC prognostic evaluation.
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页数:28
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