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Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is a common malignant tumor with a poor prognosis. Epigenetic dysregulation is now considered to be related to hepatocarcinogenesis. However, it is unclear how epigenetic-related genes (ERGs) contribute to the prognosis of HCC. In this study, we used the TCGA database...

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Autores principales: Wang, Chenchen, Yao, Chengye, Sun, Yan, Chen, Jiayi, Ge, Yangyang, Wang, Yu, Wang, Fuquan, Wang, Li, Lin, Yun, Yao, Shanglong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748485/
https://www.ncbi.nlm.nih.gov/pubmed/36531219
http://dx.doi.org/10.3389/fgene.2022.897123
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author Wang, Chenchen
Yao, Chengye
Sun, Yan
Chen, Jiayi
Ge, Yangyang
Wang, Yu
Wang, Fuquan
Wang, Li
Lin, Yun
Yao, Shanglong
author_facet Wang, Chenchen
Yao, Chengye
Sun, Yan
Chen, Jiayi
Ge, Yangyang
Wang, Yu
Wang, Fuquan
Wang, Li
Lin, Yun
Yao, Shanglong
author_sort Wang, Chenchen
collection PubMed
description Hepatocellular carcinoma (HCC) is a common malignant tumor with a poor prognosis. Epigenetic dysregulation is now considered to be related to hepatocarcinogenesis. However, it is unclear how epigenetic-related genes (ERGs) contribute to the prognosis of HCC. In this study, we used the TCGA database to identify prognostic ERGs that were differentially expressed in HCC patients. Then, using least absolute shrinkage and selection operator (LASSO) regression analysis, a six-gene signature was constructed, and patients were divided into high- and low-risk groups. Validation was performed on HCC patients from the ICGC database. Patients in the high-risk group had a significantly lower chance of survival than those in the low-risk group (p < 0.001 in both databases). The predictive ability of the signature was determined by the receiver operating characteristic (ROC) curve. The risk score was then shown to be an independent prognostic factor for the overall survival (OS) of HCC patients based on the results of univariate and multivariate analyses. We also created a practical nomogram combining the prognostic model with other clinical features. Moreover, functional enrichment analysis revealed that these genes are linked to tumor immunity. In conclusion, our findings showed that a novel six-gene signature related to epigenetics can accurately predict the occurrence and prognosis of HCC.
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spelling pubmed-97484852022-12-15 Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma Wang, Chenchen Yao, Chengye Sun, Yan Chen, Jiayi Ge, Yangyang Wang, Yu Wang, Fuquan Wang, Li Lin, Yun Yao, Shanglong Front Genet Genetics Hepatocellular carcinoma (HCC) is a common malignant tumor with a poor prognosis. Epigenetic dysregulation is now considered to be related to hepatocarcinogenesis. However, it is unclear how epigenetic-related genes (ERGs) contribute to the prognosis of HCC. In this study, we used the TCGA database to identify prognostic ERGs that were differentially expressed in HCC patients. Then, using least absolute shrinkage and selection operator (LASSO) regression analysis, a six-gene signature was constructed, and patients were divided into high- and low-risk groups. Validation was performed on HCC patients from the ICGC database. Patients in the high-risk group had a significantly lower chance of survival than those in the low-risk group (p < 0.001 in both databases). The predictive ability of the signature was determined by the receiver operating characteristic (ROC) curve. The risk score was then shown to be an independent prognostic factor for the overall survival (OS) of HCC patients based on the results of univariate and multivariate analyses. We also created a practical nomogram combining the prognostic model with other clinical features. Moreover, functional enrichment analysis revealed that these genes are linked to tumor immunity. In conclusion, our findings showed that a novel six-gene signature related to epigenetics can accurately predict the occurrence and prognosis of HCC. Frontiers Media S.A. 2022-11-30 /pmc/articles/PMC9748485/ /pubmed/36531219 http://dx.doi.org/10.3389/fgene.2022.897123 Text en Copyright © 2022 Wang, Yao, Sun, Chen, Ge, Wang, Wang, Wang, Lin and Yao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Wang, Chenchen
Yao, Chengye
Sun, Yan
Chen, Jiayi
Ge, Yangyang
Wang, Yu
Wang, Fuquan
Wang, Li
Lin, Yun
Yao, Shanglong
Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
title Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
title_full Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
title_fullStr Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
title_full_unstemmed Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
title_short Identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
title_sort identification and verification of a novel epigenetic-related gene signature for predicting the prognosis of hepatocellular carcinoma
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748485/
https://www.ncbi.nlm.nih.gov/pubmed/36531219
http://dx.doi.org/10.3389/fgene.2022.897123
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