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ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma
The gene encoding beta2-adrenergic receptor (β2-AR), adrenoceptor beta 2 (ADRB2), has been reported to closely associated with various cancers. However, its role in lung adenocarcinoma (LUAD) remains controversial. This research shed light on the prognostic value of ADRB2 in LUAD and further explore...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512930/ https://www.ncbi.nlm.nih.gov/pubmed/36163241 http://dx.doi.org/10.1038/s41598-022-19991-y |
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author | Ji, Lingyun Xu, Fei Zhang, Jingtao Song, Ting Chen, Weida Yin, Xi Wang, Qingqing Chen, Xiubao Li, Xin Guo, Minghao Chen, Zetao |
author_facet | Ji, Lingyun Xu, Fei Zhang, Jingtao Song, Ting Chen, Weida Yin, Xi Wang, Qingqing Chen, Xiubao Li, Xin Guo, Minghao Chen, Zetao |
author_sort | Ji, Lingyun |
collection | PubMed |
description | The gene encoding beta2-adrenergic receptor (β2-AR), adrenoceptor beta 2 (ADRB2), has been reported to closely associated with various cancers. However, its role in lung adenocarcinoma (LUAD) remains controversial. This research shed light on the prognostic value of ADRB2 in LUAD and further explored its association with immune cell infiltration. ADRB2 was significantly decreased in LUAD. ADRB2 expression in LUAD was significantly correlated with gender, smoking status, T classification, and pathologic stage. Patients in the low ADRB2 expression group presented with significantly poorer overall survival (OS) and disease-specific survival (DSS). Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Set Enrichment Analysis (GSEA) results showed that ADRB2 participates in immune response. The expression of ADRB2 was positively correlated with the infiltration level of most immune cells. Notably, ADRB2 is involved in LUAD progression partly by regulating the immune microenvironment, which may potentially serve as a significant prognostic biomarker as well as a potential drug target. |
format | Online Article Text |
id | pubmed-9512930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95129302022-09-28 ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma Ji, Lingyun Xu, Fei Zhang, Jingtao Song, Ting Chen, Weida Yin, Xi Wang, Qingqing Chen, Xiubao Li, Xin Guo, Minghao Chen, Zetao Sci Rep Article The gene encoding beta2-adrenergic receptor (β2-AR), adrenoceptor beta 2 (ADRB2), has been reported to closely associated with various cancers. However, its role in lung adenocarcinoma (LUAD) remains controversial. This research shed light on the prognostic value of ADRB2 in LUAD and further explored its association with immune cell infiltration. ADRB2 was significantly decreased in LUAD. ADRB2 expression in LUAD was significantly correlated with gender, smoking status, T classification, and pathologic stage. Patients in the low ADRB2 expression group presented with significantly poorer overall survival (OS) and disease-specific survival (DSS). Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Set Enrichment Analysis (GSEA) results showed that ADRB2 participates in immune response. The expression of ADRB2 was positively correlated with the infiltration level of most immune cells. Notably, ADRB2 is involved in LUAD progression partly by regulating the immune microenvironment, which may potentially serve as a significant prognostic biomarker as well as a potential drug target. Nature Publishing Group UK 2022-09-26 /pmc/articles/PMC9512930/ /pubmed/36163241 http://dx.doi.org/10.1038/s41598-022-19991-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ji, Lingyun Xu, Fei Zhang, Jingtao Song, Ting Chen, Weida Yin, Xi Wang, Qingqing Chen, Xiubao Li, Xin Guo, Minghao Chen, Zetao ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
title | ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
title_full | ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
title_fullStr | ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
title_full_unstemmed | ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
title_short | ADRB2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
title_sort | adrb2 expression predicts the clinical outcomes and is associated with immune cells infiltration in lung adenocarcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9512930/ https://www.ncbi.nlm.nih.gov/pubmed/36163241 http://dx.doi.org/10.1038/s41598-022-19991-y |
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