Identification of an immune subtype-related prognostic signature of clear cell renal cell carcinoma based on single-cell sequencing analysis

被引:0
|
作者
Fan, Zongyao [1 ,2 ]
Xu, Hewei [1 ,2 ]
Ge, Qingyu [1 ,2 ]
Li, Weilong [1 ,2 ]
Zhang, Junjie [1 ,2 ]
Pu, Yannan [3 ]
Chen, Zhengsen [1 ,2 ]
Zhang, Sicong [1 ,2 ]
Xue, Jun [1 ,2 ]
Shen, Baixin [1 ,2 ]
Ding, Liucheng [1 ,2 ]
Wei, Zhongqing [1 ,2 ]
机构
[1] Nanjing Med Univ, Dept Urol, Affiliated Hosp 2, Nanjing, Peoples R China
[2] Nanjing Med Univ, Dept Urol, Clin Med Coll 2, Nanjing, Peoples R China
[3] Nanjing Med Univ, Dept Rehabil Med, Affiliated Hosp 2, Nanjing, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2023年 / 13卷
关键词
ccRCC; single-cell sequencing analysis; immune; prognostic signature; vmp1; CANCER; EXPRESSION; PROLIFERATION; FKBP11; TUMORS; VMP1; GILT;
D O I
10.3389/fonc.2023.1067987
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundThere is growing evidence that immune cells are strongly associated with the prognosis and treatment of clear cell renal cell carcinoma (ccRCC). Our aim is to construct an immune subtype-related model to predict the prognosis of ccRCC patients and to provide guidance for finding appropriate treatment strategies. MethodsBased on single-cell analysis of the GSE152938 dataset from the GEO database, we defined the immune subtype-related genes in ccRCC. Immediately afterwards, we used Cox regression and Lasso regression to build a prognostic model based on TCGA database. Then, we carried out a series of evaluation analyses around the model. Finally, we proved the role of VMP1 in ccRCC by cellular assays. ResultInitially, based on TCGA ccRCC patient data and GEO ccRCC single-cell data, we successfully constructed a prognostic model consisting of five genes. Survival analysis showed that the higher the risk score, the worse the prognosis. We also found that the model had high predictive accuracy for patient prognosis through ROC analysis. In addition, we found that patients in the high-risk group had stronger immune cell infiltration and higher levels of immune checkpoint gene expression. Finally, cellular experiments demonstrated that when the VMP1 gene was knocked down, 786-O cells showed reduced proliferation, migration, and invasion ability and increased levels of apoptosis. ConclusionOur study can provide a reference for the diagnosis and treatment of patients with ccRCC.
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页数:13
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