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An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma

BACKGROUND: Hepatocellular carcinoma (HCC) is a major public health burden worldwide owing to high incidence and poor prognosis. Although numerous apoptotic genes were disclosed in HCC, the prognostic value and clinical utility of the genes remained unclear. METHODS: The differentially expressed gen...

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Autores principales: Chen, Kunlun, Zhu, Pengfei, Liao, Yuan, Yan, Lei, Feng, Ruo, Zhai, Wenlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936856/
https://www.ncbi.nlm.nih.gov/pubmed/33688206
http://dx.doi.org/10.2147/OTT.S293610
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author Chen, Kunlun
Zhu, Pengfei
Liao, Yuan
Yan, Lei
Feng, Ruo
Zhai, Wenlong
author_facet Chen, Kunlun
Zhu, Pengfei
Liao, Yuan
Yan, Lei
Feng, Ruo
Zhai, Wenlong
author_sort Chen, Kunlun
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) is a major public health burden worldwide owing to high incidence and poor prognosis. Although numerous apoptotic genes were disclosed in HCC, the prognostic value and clinical utility of the genes remained unclear. METHODS: The differentially expressed genes (DEGs) were identified in the microarray and RNA sequencing data from public databases. The apoptosis-related differentially expressed genes (AR-DEGs) were selected to construct a Lasso-penalized Cox regression model. The signature including five apoptotic genes was used to calculate risk score. Then, the receiver operating characteristic (ROC) and survival analysis were conducted based on the signature. A nomogram containing the signature and clinical characteristics was plotted to visualized the prognosis prediction. Finally, the enrichment analysis was performed in the Gene Ontology (GO) to investigate the potential mechanism. RESULTS: Patients with high risk scores were related to worse overall survival than those with low risk. The 3-year and 5-year area under curve (AUC) values of the signature were above 0.7 in databases. And the nomogram presented reliable net benefits for the survival prediction. The nomogram was also tested by probability calibration curves and Decision Curve Analysis (DCA). Furthermore, the five differentially expressed genes were verified again in the HCC clinical specimens with real-time PCR and Western Blot. CONCLUSION: Collectively, the present study formed a novel signature based on five apoptotic genes, and this possibly predicted prognosis and strengthened the communication with HCC patients about the likely treatment.
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spelling pubmed-79368562021-03-08 An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma Chen, Kunlun Zhu, Pengfei Liao, Yuan Yan, Lei Feng, Ruo Zhai, Wenlong Onco Targets Ther Original Research BACKGROUND: Hepatocellular carcinoma (HCC) is a major public health burden worldwide owing to high incidence and poor prognosis. Although numerous apoptotic genes were disclosed in HCC, the prognostic value and clinical utility of the genes remained unclear. METHODS: The differentially expressed genes (DEGs) were identified in the microarray and RNA sequencing data from public databases. The apoptosis-related differentially expressed genes (AR-DEGs) were selected to construct a Lasso-penalized Cox regression model. The signature including five apoptotic genes was used to calculate risk score. Then, the receiver operating characteristic (ROC) and survival analysis were conducted based on the signature. A nomogram containing the signature and clinical characteristics was plotted to visualized the prognosis prediction. Finally, the enrichment analysis was performed in the Gene Ontology (GO) to investigate the potential mechanism. RESULTS: Patients with high risk scores were related to worse overall survival than those with low risk. The 3-year and 5-year area under curve (AUC) values of the signature were above 0.7 in databases. And the nomogram presented reliable net benefits for the survival prediction. The nomogram was also tested by probability calibration curves and Decision Curve Analysis (DCA). Furthermore, the five differentially expressed genes were verified again in the HCC clinical specimens with real-time PCR and Western Blot. CONCLUSION: Collectively, the present study formed a novel signature based on five apoptotic genes, and this possibly predicted prognosis and strengthened the communication with HCC patients about the likely treatment. Dove 2021-03-02 /pmc/articles/PMC7936856/ /pubmed/33688206 http://dx.doi.org/10.2147/OTT.S293610 Text en © 2021 Chen et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Chen, Kunlun
Zhu, Pengfei
Liao, Yuan
Yan, Lei
Feng, Ruo
Zhai, Wenlong
An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma
title An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma
title_full An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma
title_fullStr An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma
title_full_unstemmed An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma
title_short An Apoptotic Gene Signature for the Prognosis of Hepatocellular Carcinoma
title_sort apoptotic gene signature for the prognosis of hepatocellular carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936856/
https://www.ncbi.nlm.nih.gov/pubmed/33688206
http://dx.doi.org/10.2147/OTT.S293610
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