The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma

PurposeTo construct a prognostic signature composed of DNA repair genes to effectively predict the prognosis of patients with head and neck squamous cell carcinoma (HNSCC).MethodsAfter downloading the transcriptome and clinical data of HNSCC from the Cancer Genome Atlas (TCGA), 499 patients with HNS...

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Main Authors: Ruijie Ming, Enhao Wang, Jiahui Wei, Jinxiong Shen, Shimin Zong, Hongjun Xiao
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-07-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2021.710694/full
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author Ruijie Ming
Enhao Wang
Jiahui Wei
Jinxiong Shen
Shimin Zong
Hongjun Xiao
author_facet Ruijie Ming
Enhao Wang
Jiahui Wei
Jinxiong Shen
Shimin Zong
Hongjun Xiao
author_sort Ruijie Ming
collection DOAJ
description PurposeTo construct a prognostic signature composed of DNA repair genes to effectively predict the prognosis of patients with head and neck squamous cell carcinoma (HNSCC).MethodsAfter downloading the transcriptome and clinical data of HNSCC from the Cancer Genome Atlas (TCGA), 499 patients with HNSCC were equally divided into training and testing sets. In the training set, 13 DNA repair genes were screened using univariate proportional hazard (Cox) regression analysis and least absolute shrinkage and selection operator (LASSO) Cox regression analysis to construct a risk model, which was validated in the testing set.ResultsIn the training and testing sets, there were significant differences in the clinical outcomes of patients in the high- and low-risk groups showed by Kaplan-Meier survival curves (P < 0.001). Univariate and multivariate Cox regression analyses showed that the risk score had independent prognostic predictive ability (P < 0.001). At the same time, the immune cell infiltration, immune score, immune-related gene expression, and tumor mutation burden (TMB) of patients with HNSCC were also different between the high- and low-risk groups (P < 0.05). Finally, we screened several chemotherapeutics for HNSCC, which showed significant differences in drug sensitivity between the high- and low-risk groups (P < 0.05).ConclusionThis study constructed a 13-DNA-repair-gene signature for the prognosis of HNSCC, which could accurately and independently predict the clinical outcome of the patient. We then revealed the immune landscape, TMB, and sensitivity to chemotherapy drugs in different risk groups, which might be used to guide clinical treatment decisions.
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spelling doaj.art-aae91584b45d4a65adf8056dcc3b6dd62022-12-21T19:59:29ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2021-07-011110.3389/fonc.2021.710694710694The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell CarcinomaRuijie MingEnhao WangJiahui WeiJinxiong ShenShimin ZongHongjun XiaoPurposeTo construct a prognostic signature composed of DNA repair genes to effectively predict the prognosis of patients with head and neck squamous cell carcinoma (HNSCC).MethodsAfter downloading the transcriptome and clinical data of HNSCC from the Cancer Genome Atlas (TCGA), 499 patients with HNSCC were equally divided into training and testing sets. In the training set, 13 DNA repair genes were screened using univariate proportional hazard (Cox) regression analysis and least absolute shrinkage and selection operator (LASSO) Cox regression analysis to construct a risk model, which was validated in the testing set.ResultsIn the training and testing sets, there were significant differences in the clinical outcomes of patients in the high- and low-risk groups showed by Kaplan-Meier survival curves (P < 0.001). Univariate and multivariate Cox regression analyses showed that the risk score had independent prognostic predictive ability (P < 0.001). At the same time, the immune cell infiltration, immune score, immune-related gene expression, and tumor mutation burden (TMB) of patients with HNSCC were also different between the high- and low-risk groups (P < 0.05). Finally, we screened several chemotherapeutics for HNSCC, which showed significant differences in drug sensitivity between the high- and low-risk groups (P < 0.05).ConclusionThis study constructed a 13-DNA-repair-gene signature for the prognosis of HNSCC, which could accurately and independently predict the clinical outcome of the patient. We then revealed the immune landscape, TMB, and sensitivity to chemotherapy drugs in different risk groups, which might be used to guide clinical treatment decisions.https://www.frontiersin.org/articles/10.3389/fonc.2021.710694/fullhead and neck squamous cell carcinomaDNA repair geneprognostic signatureimmune microenvironmenttumor mutation burdendrug sensitivity
spellingShingle Ruijie Ming
Enhao Wang
Jiahui Wei
Jinxiong Shen
Shimin Zong
Hongjun Xiao
The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma
Frontiers in Oncology
head and neck squamous cell carcinoma
DNA repair gene
prognostic signature
immune microenvironment
tumor mutation burden
drug sensitivity
title The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma
title_full The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma
title_fullStr The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma
title_full_unstemmed The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma
title_short The Prognostic Value of the DNA Repair Gene Signature in Head and Neck Squamous Cell Carcinoma
title_sort prognostic value of the dna repair gene signature in head and neck squamous cell carcinoma
topic head and neck squamous cell carcinoma
DNA repair gene
prognostic signature
immune microenvironment
tumor mutation burden
drug sensitivity
url https://www.frontiersin.org/articles/10.3389/fonc.2021.710694/full
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