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A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden

BACKGROUND: Oral squamous cell carcinoma (OSCC) is a rising problem in global public health. The traditional physical and imageological examinations are invasive and radioactive. There is a need for less harmful new biomarkers. Tumor mutational burden (TMB) is a novel prognostic biomarker for variou...

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Autores principales: Wu, Fei, Du, Yuanyuan, Hou, Xiujuan, Cheng, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052477/
https://www.ncbi.nlm.nih.gov/pubmed/35488327
http://dx.doi.org/10.1186/s12903-022-02193-3
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author Wu, Fei
Du, Yuanyuan
Hou, Xiujuan
Cheng, Wei
author_facet Wu, Fei
Du, Yuanyuan
Hou, Xiujuan
Cheng, Wei
author_sort Wu, Fei
collection PubMed
description BACKGROUND: Oral squamous cell carcinoma (OSCC) is a rising problem in global public health. The traditional physical and imageological examinations are invasive and radioactive. There is a need for less harmful new biomarkers. Tumor mutational burden (TMB) is a novel prognostic biomarker for various cancers. We intended to explore the relationship between TMB-related genes and the prognosis of OSCC and to construct a prognostic model. METHODS: TMB-related differential expressed genes (DEGs) were screened by differential analysis and optimized via the univariate Cox and LASSO Cox analyses. Risk Score model was constructed by expression values of screened genes multiplying coefficient of LASSO Cox. RESULTS: Seven TMB-related DEGs (CTSG, COL6A5, GRIA3, CCL21, ZNF662, TDRD5 and GSDMB) were screened. Patients in high-risk group (Risk Score >  − 0.684511507) had worse prognosis compared to the low-risk group (Risk Score <  − 0.684511507). Survival rates of patients in the high-risk group were lower in the gender, age and degrees of differentiation subgroups compared to the low-risk group. CONCLUSIONS: The Risk Score model constructed by 7 TMB-related genes may be a reliable biomarker for predicting the prognosis of OSCC patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-022-02193-3.
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spelling pubmed-90524772022-04-30 A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden Wu, Fei Du, Yuanyuan Hou, Xiujuan Cheng, Wei BMC Oral Health Research BACKGROUND: Oral squamous cell carcinoma (OSCC) is a rising problem in global public health. The traditional physical and imageological examinations are invasive and radioactive. There is a need for less harmful new biomarkers. Tumor mutational burden (TMB) is a novel prognostic biomarker for various cancers. We intended to explore the relationship between TMB-related genes and the prognosis of OSCC and to construct a prognostic model. METHODS: TMB-related differential expressed genes (DEGs) were screened by differential analysis and optimized via the univariate Cox and LASSO Cox analyses. Risk Score model was constructed by expression values of screened genes multiplying coefficient of LASSO Cox. RESULTS: Seven TMB-related DEGs (CTSG, COL6A5, GRIA3, CCL21, ZNF662, TDRD5 and GSDMB) were screened. Patients in high-risk group (Risk Score >  − 0.684511507) had worse prognosis compared to the low-risk group (Risk Score <  − 0.684511507). Survival rates of patients in the high-risk group were lower in the gender, age and degrees of differentiation subgroups compared to the low-risk group. CONCLUSIONS: The Risk Score model constructed by 7 TMB-related genes may be a reliable biomarker for predicting the prognosis of OSCC patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12903-022-02193-3. BioMed Central 2022-04-29 /pmc/articles/PMC9052477/ /pubmed/35488327 http://dx.doi.org/10.1186/s12903-022-02193-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wu, Fei
Du, Yuanyuan
Hou, Xiujuan
Cheng, Wei
A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
title A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
title_full A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
title_fullStr A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
title_full_unstemmed A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
title_short A prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
title_sort prognostic model for oral squamous cell carcinoma using 7 genes related to tumor mutational burden
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052477/
https://www.ncbi.nlm.nih.gov/pubmed/35488327
http://dx.doi.org/10.1186/s12903-022-02193-3
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