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pmid:33133154

Development and Validation of Nine-RNA Binding Protein Signature Predicting Overall Survival for Kidney Renal Clear Cell Carcinoma.

Weimin Zhong · Chaoqun Huang · Jianqiong Lin · Maoshu Zhu · Hongbin Zhong · Ming-Hsien Chiang · Huei-Shien Chiang · Mei-Sau Hui · Yao Lin · Jiyi Huang

Frontiers in genetics · 2020 doi:10.3389/fgene.2020.568192

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
Development and Validation of Nine-RNA Binding Protein Signature Predicting Overall Survival for Kidney Renal Clear Cell Carcinoma.
doi
10.3389/fgene.2020.568192
pmid
33133154
authors array · 10 items
[0]
Weimin Zhong
[1]
Chaoqun Huang
[2]
Jianqiong Lin
[3]
Maoshu Zhu
[4]
Hongbin Zhong
[5]
Ming-Hsien Chiang
[6]
Huei-Shien Chiang
[7]
Mei-Sau Hui
[8]
Yao Lin
[9]
Jiyi Huang
journal
Frontiers in genetics
year
2020
abstract
Cumulative studies have shown that RNA binding proteins (RBPs) play an important role in numerous malignant tumors and are related to the occurrence and progression of tumors. However, the role of RBPs in kidney renal clear cell carcinoma (KIRC) is not fully understood. In this study, we first downloaded gene expression data and corresponding clinical information of KIRC from the Cancer Genome Atlas (TCGA) database, International Cancer Genome Consortium (ICGC), and Gene Expression Omnibus (GEO) database, respectively. A total of 137 differentially expressed RBPs (DERBPs) were then identified between normal and tumor tissue, including 38 downregulated and 99 upregulated RBPs. Nine RBPs (EIF4A1, RPL36A, EXOSC5, RPL28, RPL13, RPS19, RPS2, EEF1A2, and OASL) were served as prognostic genes and exploited to construct a prognostic model through survival analysis. Kaplan-Meier curves analysis showed that the low-risk group had a better survival outcome when compared with the high-risk group. The area under the curve (AUC) value of the prognostic model was 0.713 in the TCGA data set (training data set), 0.706 in the ICGC data set, and 0.687 in the GSE29609 data set, respectively, confirming a good prognostic model. The prognostic model was also identified as an independent prognostic factor for KIRC survival by performing cox regression analysis. In addition, we also built a nomogram relying on age and the prognostic model and internal validation in the TCGA data set. The clinical benefit of the prognostic model was revealed by decision curve analysis (DCA). Gene set enrichment analysis revealed several crucial pathways (ERBB signaling pathway, pathways in cancer, MTOR signaling pathway, WNT signaling pathway, and TGF BETA signaling pathway) that may explain the underlying mechanisms of KIRC. Furthermore, potential drugs for KIRC treatment were predicted by the Connectivity Map (Cmap) database based on DERBPs, including several important drugs, such as depudecin and vorinostat, that could reverse KIRC gene expression, which may provide reference for the treatment of KIRC. In summary, we developed and validated a robust nine-RBP signature for KIRC prognosis prediction. A nomogram with risk score and age can be applied to promote the individualized prediction of overall survival in patients with KIRC. Moreover, the two drugs depudecin and vorinostat may contribute to KIRC treatment.
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Then, in order to increase the feasibility and reliability of the clinical prognosis based on RBPs, we conducted a robust likelihood-based survival analysis to further selected target RBPs by using the Rbsurv R package (Renaud et al., 2015). We downloaded the read count of KIRC, including 72 normal and 539 tumor tissues with its corresponding clinical information from TCGA1 (Table 1).
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Then, in order to increase the feasibility and reliability of the clinical prognosis based on RBPs, we conducted a robust likelihood-based survival analysis to further selected target RBPs by using the Rbsurv R package (Renaud et al., 2015).
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We downloaded the read count of KIRC, including 72 normal and 539 tumor tissues with its corresponding clinical information from TCGA1 (Table 1).
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Publicly available datasets were analyzed in this study. This data can be found here: https://portal.gdc.cancer.gov, https://www.ncbi.nlm.nih.gov/geo/, and https://dcc.icgc.org/.
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Identification and Selection of Prognostic Related RBPs
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Then, in order to increase the feasibility and reliability of the clinical prognosis based on RBPs, we conducted a robust likelihood-based survival analysis to further selected target RBPs by using the Rbsurv R package (Renaud et al., 2015). We downloaded the read count of KIRC, including 72 normal and 539 tumor tissues with its corresponding clinical information from TCGA1 (Table 1).
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:33133154", "kind": "science-record", "revision": 7, "content_hash": "sha256:93c00944676d234cfb77885b3d770a764fb2a7d4f10bf507d0159867451c4e8b", "created_at": "2026-11-01T15:41:14Z", "updated_at": "2026-11-01T22:02:26Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Development and Validation of Nine-RNA Binding Protein Signature Predicting Overall Survival for Kidney Renal Clear Cell Carcinoma.", "doi": "10.3389/fgene.2020.568192", "pmid": "33133154", "authors": ["Weimin Zhong", "Chaoqun Huang", "Jianqiong Lin", "Maoshu Zhu", "Hongbin Zhong", "Ming-Hsien Chiang", "Huei-Shien Chiang", "Mei-Sau Hui", "Yao Lin", "Jiyi Huang"], "journal": "Frontiers in genetics", "year": 2020, "abstract": "Cumulative studies have shown that RNA binding proteins (RBPs) play an important role in numerous malignant tumors and are related to the occurrence and progression of tumors. However, the role of RBPs in kidney renal clear cell carcinoma (KIRC) is not fully understood. In this study, we first downloaded gene expression data and corresponding clinical information of KIRC from the Cancer Genome Atlas (TCGA) database, International Cancer Genome Consortium (ICGC), and Gene Expression Omnibus (GEO) database, respectively. A total of 137 differentially expressed RBPs (DERBPs) were then identified between normal and tumor tissue, including 38 downregulated and 99 upregulated RBPs. Nine RBPs (EIF4A1, RPL36A, EXOSC5, RPL28, RPL13, RPS19, RPS2, EEF1A2, and OASL) were served as prognostic genes and exploited to construct a prognostic model through survival analysis. Kaplan-Meier curves analysis showed that the low-risk group had a better survival outcome when compared with the high-risk group. The area under the curve (AUC) value of the prognostic model was 0.713 in the TCGA data set (training data set), 0.706 in the ICGC data set, and 0.687 in the GSE29609 data set, respectively, confirming a good prognostic model. The prognostic model was also identified as an independent prognostic factor for KIRC survival by performing cox regression analysis. In addition, we also built a nomogram relying on age and the prognostic model and internal validation in the TCGA data set. The clinical benefit of the prognostic model was revealed by decision curve analysis (DCA). Gene set enrichment analysis revealed several crucial pathways (ERBB signaling pathway, pathways in cancer, MTOR signaling pathway, WNT signaling pathway, and TGF BETA signaling pathway) that may explain the underlying mechanisms of KIRC. Furthermore, potential drugs for KIRC treatment were predicted by the Connectivity Map (Cmap) database based on DERBPs, including several important drugs, such as depudecin and vorinostat, that could reverse KIRC gene expression, which may provide reference for the treatment of KIRC. In summary, we developed and validated a robust nine-RBP signature for KIRC prognosis prediction. A nomogram with risk score and age can be applied to promote the individualized prediction of overall survival in patients with KIRC. Moreover, the two drugs depudecin and vorinostat may contribute to KIRC treatment.", "claims": [{"id": "claim-method", "statement": "Then, in order to increase the feasibility and reliability of the clinical prognosis based on RBPs, we conducted a robust likelihood-based survival analysis to further selected target RBPs by using the Rbsurv R package (Renaud et al., 2015). 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