PeerJ | |
Microenvironment-related gene TNFSF13B predicts poor prognosis in kidney renal clear cell carcinoma | |
article | |
Mingzhe Jiang1  Jiaxing Lin1  Haotian Xing1  Jun An1  Jieping Yang1  Biao Wang2  Meng Yu3  Yuyan Zhu1  | |
[1] Department of Urology, The First Hospital of China Medical University;Department of Biochemistry and Molecular Biology, School of Life Sciences, China Medical University;Key Laboratory of Transgenetic Animal Research, Liaoning Province, Department of Laboratory Animal Science, China Medical University | |
关键词: Kidney renal clear cell carcinoma; Prognosis; Tumor microenvironment; ESTIMATE; | |
DOI : 10.7717/peerj.9453 | |
学科分类:社会科学、人文和艺术(综合) | |
来源: Inra | |
【 摘 要 】
Background Kidney renal clear cell carcinoma (KIRC) affects the genitourinary system. Although treatment of KIRC in early stages can be highly successful, this type of cancer is difficult to detect until later stages of disease that are less easily treatable. Previous studies have focused on tumor cells, but have ignored the contributions of the tumor microenvironment. Methods We analyzed KIRC gene expression data from The Cancer Genome Atlas with the ESTIMATE algorithm to identify differentially expressed genes. Through protein–protein interaction network analysis, we identified clusters and picked genes from the clusters for further analysis. Differential expression, Kaplan–Meier, and univariate Cox analyses were used to select prognostic biomarkers. Gene Set Enrichment Analysis (GSEA) and Tumor Immune Estimation Resource (TIMER) analysis were used to explore the immune characteristics of these genes as biomarkers. Results Through the ESTIMATE algorithm and other system biology tools, TNFSF13B was identified as a prognostic biomarker. TNFSF13B is highly expressed in tumors, and high expression of TNFSF13B leads to poor prognosis. Further GSEA and TIMER analysis revealed that the expression of TNFSF13B was related to the immune signaling pathway and lymphocyte infiltration. Our findings strongly suggest that TNFSF13B may be a potential biomarker or target related to the tumor microenvironment for KIRC.
【 授权许可】
CC BY
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