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The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD

BACKGROUND: Increasing evidence shows that the ubiquitin–proteasome system has a crucial impact on lung adenocarcinoma. However, reliable prognostic signatures based on ubiquitination and immune traits have not yet been established. METHODS: Bioinformatics was performed to analyze the characteristic...

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Autores principales: Che, Yinggang, Jiang, Dongbo, Xu, Leidi, Sun, Yuanjie, Wu, Yingtong, Liu, Yang, Chang, Ning, Fan, Jiangjiang, Xi, Hangtian, Qiu, Dan, Ju, Qing, Pan, Jingyu, Zhang, Yong, Yang, Kun, Zhang, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913715/
https://www.ncbi.nlm.nih.gov/pubmed/35281055
http://dx.doi.org/10.3389/fimmu.2022.846402
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author Che, Yinggang
Jiang, Dongbo
Xu, Leidi
Sun, Yuanjie
Wu, Yingtong
Liu, Yang
Chang, Ning
Fan, Jiangjiang
Xi, Hangtian
Qiu, Dan
Ju, Qing
Pan, Jingyu
Zhang, Yong
Yang, Kun
Zhang, Jian
author_facet Che, Yinggang
Jiang, Dongbo
Xu, Leidi
Sun, Yuanjie
Wu, Yingtong
Liu, Yang
Chang, Ning
Fan, Jiangjiang
Xi, Hangtian
Qiu, Dan
Ju, Qing
Pan, Jingyu
Zhang, Yong
Yang, Kun
Zhang, Jian
author_sort Che, Yinggang
collection PubMed
description BACKGROUND: Increasing evidence shows that the ubiquitin–proteasome system has a crucial impact on lung adenocarcinoma. However, reliable prognostic signatures based on ubiquitination and immune traits have not yet been established. METHODS: Bioinformatics was performed to analyze the characteristic of ubiquitination in lung adenocarcinoma. Principal component analysis was employed to identify the difference between lung adenocarcinoma and adjacent tissue. The ubiquitin prognostic risk model was constructed by multivariate Cox regression and least absolute shrinkage and selection operator regression based on the public database The Cancer Genome Atlas, with evaluation of the time-dependent receiver operating characteristic curve. A variety of algorithms was used to analyze the immune traits of model stratification. Meanwhile, the drug response sensitivity for subgroups was predicted by the “pRRophetic” package based on the database of the Cancer Genome Project. RESULTS: The expression of ubiquitin genes was different in the tumor and in the adjacent tissue. The ubiquitin model was superior to the clinical indexes, and four validation datasets verified the prognostic effect. Additionally, the stratification of the model reflected distinct immune landscapes and mutation traits. The low-risk group was infiltrating plenty of immune cells and highly expressed major histocompatibility complex and immune genes, which illustrated that these patients could benefit from immune treatment. The high-risk group showed higher mutation and tumor mutation burden. Integrating the tumor mutation burden and the immune score revealed the patient’s discrepancy between survival and drug response. Finally, we discovered that the drug targeting ubiquitin and proteasome would be a beneficial prospective treatment for lung adenocarcinoma. CONCLUSION: The ubiquitin trait could reflect the prognosis of lung adenocarcinoma, and it might shed light on the development of novel ubiquitin biomarkers and targeted therapy for lung adenocarcinoma.
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spelling pubmed-89137152022-03-12 The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD Che, Yinggang Jiang, Dongbo Xu, Leidi Sun, Yuanjie Wu, Yingtong Liu, Yang Chang, Ning Fan, Jiangjiang Xi, Hangtian Qiu, Dan Ju, Qing Pan, Jingyu Zhang, Yong Yang, Kun Zhang, Jian Front Immunol Immunology BACKGROUND: Increasing evidence shows that the ubiquitin–proteasome system has a crucial impact on lung adenocarcinoma. However, reliable prognostic signatures based on ubiquitination and immune traits have not yet been established. METHODS: Bioinformatics was performed to analyze the characteristic of ubiquitination in lung adenocarcinoma. Principal component analysis was employed to identify the difference between lung adenocarcinoma and adjacent tissue. The ubiquitin prognostic risk model was constructed by multivariate Cox regression and least absolute shrinkage and selection operator regression based on the public database The Cancer Genome Atlas, with evaluation of the time-dependent receiver operating characteristic curve. A variety of algorithms was used to analyze the immune traits of model stratification. Meanwhile, the drug response sensitivity for subgroups was predicted by the “pRRophetic” package based on the database of the Cancer Genome Project. RESULTS: The expression of ubiquitin genes was different in the tumor and in the adjacent tissue. The ubiquitin model was superior to the clinical indexes, and four validation datasets verified the prognostic effect. Additionally, the stratification of the model reflected distinct immune landscapes and mutation traits. The low-risk group was infiltrating plenty of immune cells and highly expressed major histocompatibility complex and immune genes, which illustrated that these patients could benefit from immune treatment. The high-risk group showed higher mutation and tumor mutation burden. Integrating the tumor mutation burden and the immune score revealed the patient’s discrepancy between survival and drug response. Finally, we discovered that the drug targeting ubiquitin and proteasome would be a beneficial prospective treatment for lung adenocarcinoma. CONCLUSION: The ubiquitin trait could reflect the prognosis of lung adenocarcinoma, and it might shed light on the development of novel ubiquitin biomarkers and targeted therapy for lung adenocarcinoma. Frontiers Media S.A. 2022-02-25 /pmc/articles/PMC8913715/ /pubmed/35281055 http://dx.doi.org/10.3389/fimmu.2022.846402 Text en Copyright © 2022 Che, Jiang, Xu, Sun, Wu, Liu, Chang, Fan, Xi, Qiu, Ju, Pan, Zhang, Yang and Zhang 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 Immunology
Che, Yinggang
Jiang, Dongbo
Xu, Leidi
Sun, Yuanjie
Wu, Yingtong
Liu, Yang
Chang, Ning
Fan, Jiangjiang
Xi, Hangtian
Qiu, Dan
Ju, Qing
Pan, Jingyu
Zhang, Yong
Yang, Kun
Zhang, Jian
The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD
title The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD
title_full The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD
title_fullStr The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD
title_full_unstemmed The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD
title_short The Clinical Prediction Value of the Ubiquitination Model Reflecting the Immune Traits in LUAD
title_sort clinical prediction value of the ubiquitination model reflecting the immune traits in luad
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913715/
https://www.ncbi.nlm.nih.gov/pubmed/35281055
http://dx.doi.org/10.3389/fimmu.2022.846402
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