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Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma
Liver kinase B1 (LKB1) is a tumor suppressor, and there is a very high proportion of LKB1 mutation in lung adenocarcinoma. The function of LKB1 is closely related to that of ubiquitin related genes. Our objective is to analyze the changes in ubiquitin-related genes in LKB1 mutant lung adenocarcinoma...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125361/ https://www.ncbi.nlm.nih.gov/pubmed/30185829 http://dx.doi.org/10.1038/s41598-018-31592-2 |
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author | Wang, Guanghui Bie, Fenglong Qu, Xiao Yang, Xudong Liu, Shaorui Wang, Yu Huang, Cuicui Wang, Kai Du, Jiajun |
author_facet | Wang, Guanghui Bie, Fenglong Qu, Xiao Yang, Xudong Liu, Shaorui Wang, Yu Huang, Cuicui Wang, Kai Du, Jiajun |
author_sort | Wang, Guanghui |
collection | PubMed |
description | Liver kinase B1 (LKB1) is a tumor suppressor, and there is a very high proportion of LKB1 mutation in lung adenocarcinoma. The function of LKB1 is closely related to that of ubiquitin related genes. Our objective is to analyze the changes in ubiquitin-related genes in LKB1 mutant lung adenocarcinoma. We searched The Cancer Genome Atlas (TCGA) and obtained gene expression profiles from 230 lung adenocarcinoma patients, which were then analyzed using R software. Kaplan–Meier curves and Cox proportional hazards regression were applied to estimate survival. Real-time reverse transcription PCR was used to verify gene expression. Gene function was explored by gene set enrichment analysis. There were significantly expressed differences in the ubiquitin-related gene SH3RF1 between the LKB1 mutant and wild-type lung adenocarcinoma patients (p = 9.78013E-05). Patients with LKB1 mutation and high expression of SH3RF1 had a better prognosis than the low expression group (HR 0.356, 95% CI 0.136–0.929, p = 0.035). SH3RF1 can influence cell cycle, apoptosis, DNA replication and the p53 signaling pathway. SH3RF1 might have great clinical value act as a diagnostic biomarker and indicator to evaluate the prognosis of LKB1 mutant lung adenocarcinoma patients. This gene also can become a new treatment target for LKB1 mutant lung adenocarcinoma patients. |
format | Online Article Text |
id | pubmed-6125361 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61253612018-09-10 Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma Wang, Guanghui Bie, Fenglong Qu, Xiao Yang, Xudong Liu, Shaorui Wang, Yu Huang, Cuicui Wang, Kai Du, Jiajun Sci Rep Article Liver kinase B1 (LKB1) is a tumor suppressor, and there is a very high proportion of LKB1 mutation in lung adenocarcinoma. The function of LKB1 is closely related to that of ubiquitin related genes. Our objective is to analyze the changes in ubiquitin-related genes in LKB1 mutant lung adenocarcinoma. We searched The Cancer Genome Atlas (TCGA) and obtained gene expression profiles from 230 lung adenocarcinoma patients, which were then analyzed using R software. Kaplan–Meier curves and Cox proportional hazards regression were applied to estimate survival. Real-time reverse transcription PCR was used to verify gene expression. Gene function was explored by gene set enrichment analysis. There were significantly expressed differences in the ubiquitin-related gene SH3RF1 between the LKB1 mutant and wild-type lung adenocarcinoma patients (p = 9.78013E-05). Patients with LKB1 mutation and high expression of SH3RF1 had a better prognosis than the low expression group (HR 0.356, 95% CI 0.136–0.929, p = 0.035). SH3RF1 can influence cell cycle, apoptosis, DNA replication and the p53 signaling pathway. SH3RF1 might have great clinical value act as a diagnostic biomarker and indicator to evaluate the prognosis of LKB1 mutant lung adenocarcinoma patients. This gene also can become a new treatment target for LKB1 mutant lung adenocarcinoma patients. Nature Publishing Group UK 2018-09-05 /pmc/articles/PMC6125361/ /pubmed/30185829 http://dx.doi.org/10.1038/s41598-018-31592-2 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Guanghui Bie, Fenglong Qu, Xiao Yang, Xudong Liu, Shaorui Wang, Yu Huang, Cuicui Wang, Kai Du, Jiajun Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma |
title | Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma |
title_full | Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma |
title_fullStr | Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma |
title_full_unstemmed | Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma |
title_short | Expression profiling of ubiquitin-related genes in LKB1 mutant lung adenocarcinoma |
title_sort | expression profiling of ubiquitin-related genes in lkb1 mutant lung adenocarcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125361/ https://www.ncbi.nlm.nih.gov/pubmed/30185829 http://dx.doi.org/10.1038/s41598-018-31592-2 |
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