Pan-cancer analysis of the oncogenic role of HNRNPR in human tumors

被引:3
|
作者
Yang, Yi [1 ]
Sun, Jun-Die [1 ]
Xiang, Zuo-Lin [1 ,2 ,3 ]
机构
[1] Tongji Univ, Shanghai East Hosp, Sch Med, Dept Radiat Oncol, Shanghai, Peoples R China
[2] Shanghai East Hosp Jian Hosp, Dept Radiat Oncol, Jian, Jiangxi, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai East Hosp, Dept Radiat Oncol, 150 Jimo Rd, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
biomarker; HCC; HNRNPR; pan-cancer; prognosis; GENE-EXPRESSION SIGNATURE; MUTATIONAL BURDEN; RNA; BINDING; PROTEIN; BIOMARKERS;
D O I
10.1002/cbin.12027
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Heterogeneous nuclear ribonucleoproteins (hnRNPs) are potential cancer biomarkers. Little is known about the role of HNRNPR, an essential member of the hnRNP family, in human tumours. This study aims to explore the potential value of HNRNPR across cancers, based on The Cancer Genome Atlas (TCGA). The expression level, mutation, DNA methylation, phosphorylation status, survival status, pathological stage, tumor mutation burden (TMB), microsatellite instability (MSI), immune cell infiltration, and immune signature related to HNRNPR were analyzed. HNRNPR expression level was increased in several types of cancer and was associated with poor prognosis, especially in liver hepatocellular carcinoma (LIHC). HNRNPR was also correlated with antitumour immunity, and associated with TMB, MSI, and immune cell activation status across cancers. Furthermore, nomograms were established to predict the prognosis of LIHC, based on HNRNPR and other clinical characteristics. Functional enrichment analysis showed the mechanisms of HNRNPR-mediated LIHC progression. Loss-of-function experiments demonstrated that inhibition of HNRNPR could remarkably suppress hepatocellular carcinoma (HCC) cell proliferation, migration, invasion, and Epithelial-Mesenchymal Transition abilities. Our study offers a comprehensive understanding of the oncogenic roles of HNRNPR across different tumours, and demonstrates that HNRNPR might foster the proliferation, migration, and invasion abilities of HCC cells.
引用
收藏
页码:1406 / 1426
页数:21
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