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Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration

Background: The members of the Chromobox (CBX) family are important epigenetic regulatory molecules with critical biological roles in many tumors. However, no study has analyzed or verified their role in lung adenocarcinoma (LUAD). Methods: UALCAN and Oncomine databases were used to analyze CBX expr...

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Autores principales: Zhang, Chun, Chang, Lisha, Yao, Yizhen, Chao, Ce, Ge, Zhongchun, Fan, Chengfeng, Yu, Hualin, Wang, Bin, Yang, Jingsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710700/
https://www.ncbi.nlm.nih.gov/pubmed/34966411
http://dx.doi.org/10.3389/fgene.2021.771062
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author Zhang, Chun
Chang, Lisha
Yao, Yizhen
Chao, Ce
Ge, Zhongchun
Fan, Chengfeng
Yu, Hualin
Wang, Bin
Yang, Jingsong
author_facet Zhang, Chun
Chang, Lisha
Yao, Yizhen
Chao, Ce
Ge, Zhongchun
Fan, Chengfeng
Yu, Hualin
Wang, Bin
Yang, Jingsong
author_sort Zhang, Chun
collection PubMed
description Background: The members of the Chromobox (CBX) family are important epigenetic regulatory molecules with critical biological roles in many tumors. However, no study has analyzed or verified their role in lung adenocarcinoma (LUAD). Methods: UALCAN and Oncomine databases were used to analyze CBX expression in LUAD, and the cBioPortal database was used to analyze CBX genetic variations. The Kaplan-Meier plotter and UALCAN databases were used to identify molecules with prognostic value. Gene Ontology pathway, receiver operating characteristic curves, and tumor-infiltrating immune cell analyses were used to clarify the biological function of the CBX hub molecules. Paired tumor samples and lung adenocarcinoma cell lines were collected for molecular functional assays to validate the results of the bioinformatics analysis. Results: CBX3/5 may have a cancer-promoting effect and its expression is associated with a poor patient prognosis, while CBX7 shows an opposite trend. CBX3/5/7 can regulate signaling pathways, regulate tumor immune cell infiltration, and has diagnostic value. Molecular biology experiments show that CBX3/5 is highly expressed in LUAD patients; in vitro it promotes the proliferation and migration of the LUAD cell line and can regulate the expression of the corresponding cytokines. CBX7 has opposite effects. Conclusion: Our bioinformatics analysis and subsequent experimental verification confirmed the CBX family members acted as hub signaling molecules in LUAD. The results provide new potential targets for the diagnosis and treatment of this cancer.
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spelling pubmed-87107002021-12-28 Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration Zhang, Chun Chang, Lisha Yao, Yizhen Chao, Ce Ge, Zhongchun Fan, Chengfeng Yu, Hualin Wang, Bin Yang, Jingsong Front Genet Genetics Background: The members of the Chromobox (CBX) family are important epigenetic regulatory molecules with critical biological roles in many tumors. However, no study has analyzed or verified their role in lung adenocarcinoma (LUAD). Methods: UALCAN and Oncomine databases were used to analyze CBX expression in LUAD, and the cBioPortal database was used to analyze CBX genetic variations. The Kaplan-Meier plotter and UALCAN databases were used to identify molecules with prognostic value. Gene Ontology pathway, receiver operating characteristic curves, and tumor-infiltrating immune cell analyses were used to clarify the biological function of the CBX hub molecules. Paired tumor samples and lung adenocarcinoma cell lines were collected for molecular functional assays to validate the results of the bioinformatics analysis. Results: CBX3/5 may have a cancer-promoting effect and its expression is associated with a poor patient prognosis, while CBX7 shows an opposite trend. CBX3/5/7 can regulate signaling pathways, regulate tumor immune cell infiltration, and has diagnostic value. Molecular biology experiments show that CBX3/5 is highly expressed in LUAD patients; in vitro it promotes the proliferation and migration of the LUAD cell line and can regulate the expression of the corresponding cytokines. CBX7 has opposite effects. Conclusion: Our bioinformatics analysis and subsequent experimental verification confirmed the CBX family members acted as hub signaling molecules in LUAD. The results provide new potential targets for the diagnosis and treatment of this cancer. Frontiers Media S.A. 2021-12-13 /pmc/articles/PMC8710700/ /pubmed/34966411 http://dx.doi.org/10.3389/fgene.2021.771062 Text en Copyright © 2021 Zhang, Chang, Yao, Chao, Ge, Fan, Yu, Wang and Yang. 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
Zhang, Chun
Chang, Lisha
Yao, Yizhen
Chao, Ce
Ge, Zhongchun
Fan, Chengfeng
Yu, Hualin
Wang, Bin
Yang, Jingsong
Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration
title Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration
title_full Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration
title_fullStr Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration
title_full_unstemmed Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration
title_short Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration
title_sort role of the cbx molecular family in lung adenocarcinoma tumorigenesis and immune infiltration
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710700/
https://www.ncbi.nlm.nih.gov/pubmed/34966411
http://dx.doi.org/10.3389/fgene.2021.771062
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