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Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is one of the most malignant tumors with persistently high morbidity and mortality. However, the expression, prognostic and clinical significance of FAM189 family genes in HCC remain largely unknown. In this study, the expression levels of FAM189 family genes in HCC we...

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Autores principales: Ma, Wanshan, Zhang, Xiaoning, Ma, Chenchen, Liu, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732019/
https://www.ncbi.nlm.nih.gov/pubmed/36507118
http://dx.doi.org/10.3389/pore.2022.1610674
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author Ma, Wanshan
Zhang, Xiaoning
Ma, Chenchen
Liu, Peng
author_facet Ma, Wanshan
Zhang, Xiaoning
Ma, Chenchen
Liu, Peng
author_sort Ma, Wanshan
collection PubMed
description Hepatocellular carcinoma (HCC) is one of the most malignant tumors with persistently high morbidity and mortality. However, the expression, prognostic and clinical significance of FAM189 family genes in HCC remain largely unknown. In this study, the expression levels of FAM189 family genes in HCC were analyzed through TCGA-LIHC and ICGC-LIRI-JP cohorts, and further validated in multiple independent GEO datasets. It was found that the expression of FAM189B was significantly upregulated in HCC tumor tissues, while the expression of FAM189A1 and FAM189A2 was not significantly changed between tumor and adjacent tissues. Further analysis revealed that upregulated copy number variation contributed to increased expression of FAM189B in HCC. Survival analysis showed that highly expressed FAM189B was significantly correlated with unfavorable prognosis, including overall survival, disease-specific survival, and progression-free interval. Univariate and multivariate Cox regression analysis showed that FAM189B was a potential novel prognosis factor for HCC patients. In addition, the association between FAM189B expression and clinical and molecular characteristics was analyzed. High expression of FAM189B was associated with high AFP level, high predicted risk metastasis signature, and TP53 mutation, while there was no significant association between FAM189B expression and cancer stage or tumor grade of HCC. Gene set enrichment analysis revealed that highly expressed FAM189B was closely related with signal pathways and biological processes associated with cell proliferation and cell cycle in HCC. In conclusion, this study suggested that FAM189B was highly expressed in HCC and highly expressed FAM189B may serve as an effective prognostic indicator and a potential therapeutic target for HCC patients.
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spelling pubmed-97320192022-12-10 Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma Ma, Wanshan Zhang, Xiaoning Ma, Chenchen Liu, Peng Pathol Oncol Res Pathology and Oncology Archive Hepatocellular carcinoma (HCC) is one of the most malignant tumors with persistently high morbidity and mortality. However, the expression, prognostic and clinical significance of FAM189 family genes in HCC remain largely unknown. In this study, the expression levels of FAM189 family genes in HCC were analyzed through TCGA-LIHC and ICGC-LIRI-JP cohorts, and further validated in multiple independent GEO datasets. It was found that the expression of FAM189B was significantly upregulated in HCC tumor tissues, while the expression of FAM189A1 and FAM189A2 was not significantly changed between tumor and adjacent tissues. Further analysis revealed that upregulated copy number variation contributed to increased expression of FAM189B in HCC. Survival analysis showed that highly expressed FAM189B was significantly correlated with unfavorable prognosis, including overall survival, disease-specific survival, and progression-free interval. Univariate and multivariate Cox regression analysis showed that FAM189B was a potential novel prognosis factor for HCC patients. In addition, the association between FAM189B expression and clinical and molecular characteristics was analyzed. High expression of FAM189B was associated with high AFP level, high predicted risk metastasis signature, and TP53 mutation, while there was no significant association between FAM189B expression and cancer stage or tumor grade of HCC. Gene set enrichment analysis revealed that highly expressed FAM189B was closely related with signal pathways and biological processes associated with cell proliferation and cell cycle in HCC. In conclusion, this study suggested that FAM189B was highly expressed in HCC and highly expressed FAM189B may serve as an effective prognostic indicator and a potential therapeutic target for HCC patients. Frontiers Media S.A. 2022-11-25 /pmc/articles/PMC9732019/ /pubmed/36507118 http://dx.doi.org/10.3389/pore.2022.1610674 Text en Copyright © 2022 Ma, Zhang, Ma and Liu. 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 Pathology and Oncology Archive
Ma, Wanshan
Zhang, Xiaoning
Ma, Chenchen
Liu, Peng
Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma
title Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma
title_full Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma
title_fullStr Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma
title_full_unstemmed Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma
title_short Highly expressed FAM189B predicts poor prognosis in hepatocellular carcinoma
title_sort highly expressed fam189b predicts poor prognosis in hepatocellular carcinoma
topic Pathology and Oncology Archive
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732019/
https://www.ncbi.nlm.nih.gov/pubmed/36507118
http://dx.doi.org/10.3389/pore.2022.1610674
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