Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma

BackgroundLung adenocarcinoma (LUAD) is the major non-small-cell lung cancer pathological subtype with poor prognosis worldwide. Herein, we aimed to build an energy metabolism-associated prognostic gene signature to predict patient survival.MethodsThe gene expression profiles of patients with LUAD w...

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Main Authors: Teng Mu, Haoran Li, Xiangnan Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-04-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.867470/full
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author Teng Mu
Haoran Li
Xiangnan Li
author_facet Teng Mu
Haoran Li
Xiangnan Li
author_sort Teng Mu
collection DOAJ
description BackgroundLung adenocarcinoma (LUAD) is the major non-small-cell lung cancer pathological subtype with poor prognosis worldwide. Herein, we aimed to build an energy metabolism-associated prognostic gene signature to predict patient survival.MethodsThe gene expression profiles of patients with LUAD were downloaded from the TCGA and GEO databases, and energy metabolism (EM)-related genes were downloaded from the GeneCards database. Univariate Cox and LASSO analyses were performed to identify the prognostic EM-associated gene signatures. Kaplan–Meier and receiver operating characteristic (ROC) curves were plotted to validate the predictive effect of the prognostic signatures. A CIBERSORT analysis was used to evaluate the correlation between the risk model and immune cells. A nomogram was used to predict the survival probability of LUAD based on a risk model.ResultsWe constructed a prognostic signature comprising 13 EM-related genes (AGER, AHSG, ALDH2, CIDEC, CYP17A1, FBP1, GNB3, GZMB, IGFBP1, SORD, SOX2, TRH and TYMS). The Kaplan–Meier curves validated the good predictive ability of the prognostic signature in TCGA AND two GEO datasets (p<0.0001, p=0.00021, and p=0.0034, respectively). The area under the curve (AUC) of the ROC curves also validated the predictive accuracy of the risk model. We built a nomogram to predict the survival probability of LUAD, and the calibration curves showed good predictive ability. Finally, a functional analysis also unveiled the different immune statuses between the two different risk groups.ConclusionOur study constructed and verified a novel EM-related prognostic gene signature that could improve the individualized prediction of survival probability in LUAD.
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spelling doaj.art-1c349f4562c44844ad3acff0d691c63e2022-12-22T01:07:19ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-04-011210.3389/fonc.2022.867470867470Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung AdenocarcinomaTeng Mu0Haoran Li1Xiangnan Li2Department of Thoracic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, ChinaDepartment of Thoracic Surgery, Peking University People’s Hospital, Beijing, ChinaDepartment of Thoracic Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, ChinaBackgroundLung adenocarcinoma (LUAD) is the major non-small-cell lung cancer pathological subtype with poor prognosis worldwide. Herein, we aimed to build an energy metabolism-associated prognostic gene signature to predict patient survival.MethodsThe gene expression profiles of patients with LUAD were downloaded from the TCGA and GEO databases, and energy metabolism (EM)-related genes were downloaded from the GeneCards database. Univariate Cox and LASSO analyses were performed to identify the prognostic EM-associated gene signatures. Kaplan–Meier and receiver operating characteristic (ROC) curves were plotted to validate the predictive effect of the prognostic signatures. A CIBERSORT analysis was used to evaluate the correlation between the risk model and immune cells. A nomogram was used to predict the survival probability of LUAD based on a risk model.ResultsWe constructed a prognostic signature comprising 13 EM-related genes (AGER, AHSG, ALDH2, CIDEC, CYP17A1, FBP1, GNB3, GZMB, IGFBP1, SORD, SOX2, TRH and TYMS). The Kaplan–Meier curves validated the good predictive ability of the prognostic signature in TCGA AND two GEO datasets (p<0.0001, p=0.00021, and p=0.0034, respectively). The area under the curve (AUC) of the ROC curves also validated the predictive accuracy of the risk model. We built a nomogram to predict the survival probability of LUAD, and the calibration curves showed good predictive ability. Finally, a functional analysis also unveiled the different immune statuses between the two different risk groups.ConclusionOur study constructed and verified a novel EM-related prognostic gene signature that could improve the individualized prediction of survival probability in LUAD.https://www.frontiersin.org/articles/10.3389/fonc.2022.867470/fulllung adenocarcinomaenergy metabolismrisk modelprognosisnomogram
spellingShingle Teng Mu
Haoran Li
Xiangnan Li
Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma
Frontiers in Oncology
lung adenocarcinoma
energy metabolism
risk model
prognosis
nomogram
title Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma
title_full Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma
title_fullStr Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma
title_full_unstemmed Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma
title_short Prognostic Implication of Energy Metabolism-Related Gene Signatures in Lung Adenocarcinoma
title_sort prognostic implication of energy metabolism related gene signatures in lung adenocarcinoma
topic lung adenocarcinoma
energy metabolism
risk model
prognosis
nomogram
url https://www.frontiersin.org/articles/10.3389/fonc.2022.867470/full
work_keys_str_mv AT tengmu prognosticimplicationofenergymetabolismrelatedgenesignaturesinlungadenocarcinoma
AT haoranli prognosticimplicationofenergymetabolismrelatedgenesignaturesinlungadenocarcinoma
AT xiangnanli prognosticimplicationofenergymetabolismrelatedgenesignaturesinlungadenocarcinoma