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Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma

Liver cancer is the fifth most prevalent malignant tumor, while hepatocellular carcinoma represents the most prevalent subtype worldwide. Previous studies have associated the chromobox family, critical components of epigenetic regulatory complexes, with development of many malignancies owing to thei...

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Autores principales: Pan, Chenxi, Luo, Nan, Guo, Kun, Wang, Wenbo, Li, Lei, Fan, Ning, Tian, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168656/
https://www.ncbi.nlm.nih.gov/pubmed/35677563
http://dx.doi.org/10.3389/fgene.2022.887925
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author Pan, Chenxi
Luo, Nan
Guo, Kun
Wang, Wenbo
Li, Lei
Fan, Ning
Tian, Yu
author_facet Pan, Chenxi
Luo, Nan
Guo, Kun
Wang, Wenbo
Li, Lei
Fan, Ning
Tian, Yu
author_sort Pan, Chenxi
collection PubMed
description Liver cancer is the fifth most prevalent malignant tumor, while hepatocellular carcinoma represents the most prevalent subtype worldwide. Previous studies have associated the chromobox family, critical components of epigenetic regulatory complexes, with development of many malignancies owing to their role in inhibiting differentiation and promoting proliferation of cancer cells. However, little is known regarding their function in development and progression of hepatocellular carcinoma. In the present study, we analyzed differential expression, prognostic value, immune cell infiltration, and gene pathway enrichment of chromobox family in hepatocellular carcinoma patients. Next, we performed Pearson’s correlation analysis to determine the relationships between chromobox family proteins with tumor-immune infiltration. Results revealed that high expression of CBX1, CBX2, CBX3, CBX6, and CBX8 was associated with poor survival rates of hepatocellular carcinoma patients. These five factors were used to build prognostic gene models using LASSO Cox regression analysis. Results indicated that high expression of CBX2 and CBX3 proteins was significantly associated with poor prognosis for hepatocellular carcinoma patients. The resulting nomogram revealed that CBX3 and T stages were significantly correlated with prognosis of hepatocellular carcinoma patients. Notably, predictive CBX3 was strongly correlated with immune cell infiltration. Furthermore, results from functional enrichment analysis revealed that CBX3 was mainly involved in regulation of methylation of Histone H3-K27. Collectively, these findings suggest that CBX3 could be a biomarker for predicting prognosis of hepatocellular carcinoma patients.
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spelling pubmed-91686562022-06-07 Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma Pan, Chenxi Luo, Nan Guo, Kun Wang, Wenbo Li, Lei Fan, Ning Tian, Yu Front Genet Genetics Liver cancer is the fifth most prevalent malignant tumor, while hepatocellular carcinoma represents the most prevalent subtype worldwide. Previous studies have associated the chromobox family, critical components of epigenetic regulatory complexes, with development of many malignancies owing to their role in inhibiting differentiation and promoting proliferation of cancer cells. However, little is known regarding their function in development and progression of hepatocellular carcinoma. In the present study, we analyzed differential expression, prognostic value, immune cell infiltration, and gene pathway enrichment of chromobox family in hepatocellular carcinoma patients. Next, we performed Pearson’s correlation analysis to determine the relationships between chromobox family proteins with tumor-immune infiltration. Results revealed that high expression of CBX1, CBX2, CBX3, CBX6, and CBX8 was associated with poor survival rates of hepatocellular carcinoma patients. These five factors were used to build prognostic gene models using LASSO Cox regression analysis. Results indicated that high expression of CBX2 and CBX3 proteins was significantly associated with poor prognosis for hepatocellular carcinoma patients. The resulting nomogram revealed that CBX3 and T stages were significantly correlated with prognosis of hepatocellular carcinoma patients. Notably, predictive CBX3 was strongly correlated with immune cell infiltration. Furthermore, results from functional enrichment analysis revealed that CBX3 was mainly involved in regulation of methylation of Histone H3-K27. Collectively, these findings suggest that CBX3 could be a biomarker for predicting prognosis of hepatocellular carcinoma patients. Frontiers Media S.A. 2022-05-23 /pmc/articles/PMC9168656/ /pubmed/35677563 http://dx.doi.org/10.3389/fgene.2022.887925 Text en Copyright © 2022 Pan, Luo, Guo, Wang, Li, Fan and Tian. 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
Pan, Chenxi
Luo, Nan
Guo, Kun
Wang, Wenbo
Li, Lei
Fan, Ning
Tian, Yu
Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma
title Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma
title_full Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma
title_fullStr Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma
title_full_unstemmed Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma
title_short Members of the Chromobox Family Have Prognostic Value in Hepatocellular Carcinoma
title_sort members of the chromobox family have prognostic value in hepatocellular carcinoma
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168656/
https://www.ncbi.nlm.nih.gov/pubmed/35677563
http://dx.doi.org/10.3389/fgene.2022.887925
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