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pmid:37035172

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

Zongyao Fan · Hewei Xu · Qingyu Ge · Weilong Li · Junjie Zhang · Yannan Pu · Zhengsen Chen · Sicong Zhang · Jun Xue · Baixin Shen · Liucheng Ding · Zhongqing Wei

Frontiers in oncology · 2023 doi:10.3389/fonc.2023.1067987

Paper

complete

Experiment

complete

Data

partial

Analysis

complete

Execution

absent

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Identification of an immune subtype-related prognostic signature of clear cell renal cell carcinoma based on single-cell sequencing analysis.
doi
10.3389/fonc.2023.1067987
pmid
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Zongyao Fan
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Hewei Xu
[2]
Qingyu Ge
[3]
Weilong Li
[4]
Junjie Zhang
[5]
Yannan Pu
[6]
Zhengsen Chen
[7]
Sicong Zhang
[8]
Jun Xue
[9]
Baixin Shen
[10]
Liucheng Ding
[11]
Zhongqing Wei
journal
Frontiers in oncology
year
2023
abstract
Background: There 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. Methods: Based 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. Result: Initially, 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. Conclusion: Our study can provide a reference for the diagnosis and treatment of patients with ccRCC.
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Initially, based on TCGA ccRCC patient data and GEO ccRCC single-cell data, we successfully constructed a prognostic model consisting of five genes.
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Single-Cell RNA Sequencing in Multiple Pathologic Types of Renal Cell Carcinoma Revealed Novel Potential Tumor-Specific Markers
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and invasion ability and increased levels of apoptosis. Conclusion: Our study can provide a referen
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RCC patients in two groups. Cell culture and transfection CcRCC cell-lines 786-O was purchased from th
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