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PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration

BACKGROUND: Lung adenocarcinoma (LUAD) is one of the tumor‐related diseases with high morbidity worldwide. Epigenetic modifications such as DNA methylation changes may involve in tumorigenesis. This study aimed to explore new biomarkers that have prognostic significance of LUAD. METHODS: First, we d...

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Autores principales: Wang, Jinjie, Shi, Muqi, Zhang, Haijian, Zhou, Hao, Huang, Zhanghao, Zhou, Youlang, Shi, Jiahai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200888/
https://www.ncbi.nlm.nih.gov/pubmed/35567329
http://dx.doi.org/10.1111/1759-7714.14466
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author Wang, Jinjie
Shi, Muqi
Zhang, Haijian
Zhou, Hao
Huang, Zhanghao
Zhou, Youlang
Shi, Jiahai
author_facet Wang, Jinjie
Shi, Muqi
Zhang, Haijian
Zhou, Hao
Huang, Zhanghao
Zhou, Youlang
Shi, Jiahai
author_sort Wang, Jinjie
collection PubMed
description BACKGROUND: Lung adenocarcinoma (LUAD) is one of the tumor‐related diseases with high morbidity worldwide. Epigenetic modifications such as DNA methylation changes may involve in tumorigenesis. This study aimed to explore new biomarkers that have prognostic significance of LUAD. METHODS: First, we downloaded the gene expression and methylation data set from Gene Expression Omnibus. R software was then used to identify abnormally methylated differentially expressed genes (MDEGs). Next, R package Cluster Profiler was used to analyze the enrichment and pathway of the MDEGs. Analysis using STRING revealed the protein–protein interaction network. The result was then visualized by Cytoscape and obtained 10 hub genes. Afterward, they were further verified by The Cancer Genome Atlas to select candidate genes. Moreover, quantitative real‐time polymerase chain reaction (qRT‐PCR) and immunohistochemistry were used to verify the expression and prognostic value of candidate genes in LUAD patients. RESULTS: The results showed that the expressions of ADCY5 and PRKCB are indeed related to LUAD. The clinical relevance to PRKCB was confirmed by its clinical correlation analysis. Gene set enrichment analysis (GSEA) and tumor immune estimation resource (TIMER) tumor immune correlations showed that PRKCB is involved in the cancer‐related Kyoto Encyclopedia of Genes and Genomes pathway and is involved in immune infiltration. It was also verified by qRT‐PCR and immunohistochemistry that PRKCB was lowly expressed in LUAD patients and correlated with prognosis. CONCLUSIONS: PRKCB is relevant to prognosis of LUAD through methylation and immune infiltration.
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spelling pubmed-92008882022-06-23 PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration Wang, Jinjie Shi, Muqi Zhang, Haijian Zhou, Hao Huang, Zhanghao Zhou, Youlang Shi, Jiahai Thorac Cancer Original Articles BACKGROUND: Lung adenocarcinoma (LUAD) is one of the tumor‐related diseases with high morbidity worldwide. Epigenetic modifications such as DNA methylation changes may involve in tumorigenesis. This study aimed to explore new biomarkers that have prognostic significance of LUAD. METHODS: First, we downloaded the gene expression and methylation data set from Gene Expression Omnibus. R software was then used to identify abnormally methylated differentially expressed genes (MDEGs). Next, R package Cluster Profiler was used to analyze the enrichment and pathway of the MDEGs. Analysis using STRING revealed the protein–protein interaction network. The result was then visualized by Cytoscape and obtained 10 hub genes. Afterward, they were further verified by The Cancer Genome Atlas to select candidate genes. Moreover, quantitative real‐time polymerase chain reaction (qRT‐PCR) and immunohistochemistry were used to verify the expression and prognostic value of candidate genes in LUAD patients. RESULTS: The results showed that the expressions of ADCY5 and PRKCB are indeed related to LUAD. The clinical relevance to PRKCB was confirmed by its clinical correlation analysis. Gene set enrichment analysis (GSEA) and tumor immune estimation resource (TIMER) tumor immune correlations showed that PRKCB is involved in the cancer‐related Kyoto Encyclopedia of Genes and Genomes pathway and is involved in immune infiltration. It was also verified by qRT‐PCR and immunohistochemistry that PRKCB was lowly expressed in LUAD patients and correlated with prognosis. CONCLUSIONS: PRKCB is relevant to prognosis of LUAD through methylation and immune infiltration. John Wiley & Sons Australia, Ltd 2022-05-13 2022-06 /pmc/articles/PMC9200888/ /pubmed/35567329 http://dx.doi.org/10.1111/1759-7714.14466 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Jinjie
Shi, Muqi
Zhang, Haijian
Zhou, Hao
Huang, Zhanghao
Zhou, Youlang
Shi, Jiahai
PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
title PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
title_full PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
title_fullStr PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
title_full_unstemmed PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
title_short PRKCB is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
title_sort prkcb is relevant to prognosis of lung adenocarcinoma through methylation and immune infiltration
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9200888/
https://www.ncbi.nlm.nih.gov/pubmed/35567329
http://dx.doi.org/10.1111/1759-7714.14466
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