CCDC137 Is a Prognostic Biomarker and Correlates With Immunosuppressive Tumor Microenvironment Based on Pan-Cancer Analysis

肿瘤微环境 黑色素瘤 癌基因 癌症研究 生物 生物标志物 癌症 胶质瘤 肿瘤科 免疫系统 医学 免疫学 细胞周期 遗传学
作者
Lihao Guo,Boxin Li,Zhaohong Lu,Hairong Liang,Hui Yang,Yuting Chen,Shiheng Zhu,Minjuan Zeng,Yixian Wei,Tonggong Liu,Tikeng Jiang,Mei Ying Xuan,Huanwen Tang
出处
期刊:Frontiers in Molecular Biosciences [Frontiers Media SA]
卷期号:8 被引量:21
标识
DOI:10.3389/fmolb.2021.674863
摘要

Background The coiled-coil domain containing (CCDC) family proteins have important biological functions in various diseases. However, the coiled-coil domain containing 137 (CCDC137) was rarely studied. We aim to investigate the role of CCDC137 in pan-cancer. Methods CCDC137 expression was evaluated in RNA sequence expression profilers of pan-cancer and normal tissues from The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) database. The influence of CCDC137 on the prognosis of tumor patients was analyzed using clinical survival data from TCGA. Function and pathway enrichment analysis was performed to explore the role of CCDC137 using the R package “clusterProfiler.” We further analyzed the correlation of immune cell infiltration score of TCGA samples and CCDC137 expression using TIMER2 online database. Results CCDC137 was over-expressed and associated with worse survival status in various tumor types. CCDC137 expression was positively correlated with tumor associated macrophages (TAMs) and cancer associated fibroblasts (CAFs) in Lower Grade Glioma (LGG) and Uveal Melanoma (UVM). In addition, high CCDC137 expression was positively correlated with most immunosuppressive genes, including TGFB1, PD-L1, and IL10RB in LGG and UVM. Conclusions Our study identified CCDC137 as an oncogene and predictor of worse survival in most tumor types. High CCDC137 may contribute to elevated infiltration of TAMs and CAFs and be associated with tumor immunosuppressive status.
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