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Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients

BACKGROUND: Hepatocellular carcinoma (HCC) is a common malignant primary cancer with high mortality. Previous studies have demonstrated that RNA binding proteins (RBPs) are involved in the biological processes of cancers, including hepatocellular cancer. METHODS: In this study, we aimed to identify...

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Autores principales: Wang, Li, Zhou, Na, Qu, Jialin, Jiang, Man, Zhang, Xiaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727152/
https://www.ncbi.nlm.nih.gov/pubmed/33297932
http://dx.doi.org/10.1186/s10020-020-00252-5
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author Wang, Li
Zhou, Na
Qu, Jialin
Jiang, Man
Zhang, Xiaochun
author_facet Wang, Li
Zhou, Na
Qu, Jialin
Jiang, Man
Zhang, Xiaochun
author_sort Wang, Li
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) is a common malignant primary cancer with high mortality. Previous studies have demonstrated that RNA binding proteins (RBPs) are involved in the biological processes of cancers, including hepatocellular cancer. METHODS: In this study, we aimed to identify the clinical value of RNA-binding proteins for hepatocellular carcinoma. We obtained gene expression and clinical data of hepatocellular carcinoma patients from the TCGA and ICGC databases. The prognostic value of RBP-related genes in patients with hepatocellular carcinoma and their function were studied by comprehensive bioinformatics analyses. The gene signature of SMG5, EZH2, FBLL1, ZNF239, and IGF2BP3 was generated by univariate and multivariate Cox regression and LASSO regression analyses. We built and verified a prognostic nomogram based on RBP-related genes. The gene signature was validated by the ICGC database. The expression of RBP-related genes was validated by the Oncomine database, the Human Protein Atlas and Kaplan–Meier plotter. RESULT: Most RBP-related genes were significantly different in cancer and normal tissues. The survival of patients in the different groups was significantly different. The gene signature showed good performance for predicting the survival of HCC patients by having a better area under the receiver operating characteristic curve than other clinicopathological parameters. CONCLUSION: Gene signatures based on RNA-binding proteins can be independent risk factors for hepatocellular carcinoma patients.
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spelling pubmed-77271522020-12-11 Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients Wang, Li Zhou, Na Qu, Jialin Jiang, Man Zhang, Xiaochun Mol Med Research Article BACKGROUND: Hepatocellular carcinoma (HCC) is a common malignant primary cancer with high mortality. Previous studies have demonstrated that RNA binding proteins (RBPs) are involved in the biological processes of cancers, including hepatocellular cancer. METHODS: In this study, we aimed to identify the clinical value of RNA-binding proteins for hepatocellular carcinoma. We obtained gene expression and clinical data of hepatocellular carcinoma patients from the TCGA and ICGC databases. The prognostic value of RBP-related genes in patients with hepatocellular carcinoma and their function were studied by comprehensive bioinformatics analyses. The gene signature of SMG5, EZH2, FBLL1, ZNF239, and IGF2BP3 was generated by univariate and multivariate Cox regression and LASSO regression analyses. We built and verified a prognostic nomogram based on RBP-related genes. The gene signature was validated by the ICGC database. The expression of RBP-related genes was validated by the Oncomine database, the Human Protein Atlas and Kaplan–Meier plotter. RESULT: Most RBP-related genes were significantly different in cancer and normal tissues. The survival of patients in the different groups was significantly different. The gene signature showed good performance for predicting the survival of HCC patients by having a better area under the receiver operating characteristic curve than other clinicopathological parameters. CONCLUSION: Gene signatures based on RNA-binding proteins can be independent risk factors for hepatocellular carcinoma patients. BioMed Central 2020-12-09 /pmc/articles/PMC7727152/ /pubmed/33297932 http://dx.doi.org/10.1186/s10020-020-00252-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Wang, Li
Zhou, Na
Qu, Jialin
Jiang, Man
Zhang, Xiaochun
Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients
title Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients
title_full Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients
title_fullStr Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients
title_full_unstemmed Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients
title_short Identification of an RNA binding protein-related gene signature in hepatocellular carcinoma patients
title_sort identification of an rna binding protein-related gene signature in hepatocellular carcinoma patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727152/
https://www.ncbi.nlm.nih.gov/pubmed/33297932
http://dx.doi.org/10.1186/s10020-020-00252-5
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