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Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes
BACKGROUND: The prevalence of thyroid cancer (ThyC), a frequent malignant tumor of the endocrine system, has been rapidly increasing over time. The mitophagy pathway is reported to play a critical role in ThyC onset and progression in many studies. This research aims to create a mitophagy-related su...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501032/ https://www.ncbi.nlm.nih.gov/pubmed/37707688 http://dx.doi.org/10.1007/s12672-023-00772-6 |
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author | Sun, Wencong Wang, Xinhui Li, Guoqing Ding, Chao Wang, Yichen Su, Zijie Xue, Meifang |
author_facet | Sun, Wencong Wang, Xinhui Li, Guoqing Ding, Chao Wang, Yichen Su, Zijie Xue, Meifang |
author_sort | Sun, Wencong |
collection | PubMed |
description | BACKGROUND: The prevalence of thyroid cancer (ThyC), a frequent malignant tumor of the endocrine system, has been rapidly increasing over time. The mitophagy pathway is reported to play a critical role in ThyC onset and progression in many studies. This research aims to create a mitophagy-related survival prediction model for ThyC patients. METHODS: Genes connected to mitophagy were found in the GeneCards database. The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases provided information on the expression patterns of ThyC-related genes. To identify differentially expressed genes (DEGs), R software was employed. The prognostic significance of each DEG was assessed using the prognostic K-M curve. The prognostic model was built using LASSO, ROC, univariate, and multivariate Cox regression analyses. Finally, a nomogram model was developed to predict the survival outcome of ThyC patients in the clinical setting. RESULTS: Through differential analysis, functional enrichment analysis, and protein–protein interaction (PPI) network analysis, we screened 10 key genes related to mitophagy in ThyC. The risk model was eventually developed using LASSO and Cox regression analyses based on the six DEGs related to mitophagy. An altered expression level of a mitophagy-related prognostic gene, GGCT, was found to be the most significant one, according to the KM survival curve analysis. An immunohistochemical (IHC) investigation revealed that ThyC tissues expressed higher levels of GGCT than normal thyroid tissues. The ROC curve verified the satisfactory performance of the model in survival prediction. Multivariate Cox regression analysis showed that the pathological grade, residual tumor volume, and initial tumor lesion type were significantly linked to the prognosis. Finally, we created a nomogram to predict the overall survival rate of ThyC patients at 3-, 5-, and 7- year time points. CONCLUSION: The nomogram risk prediction model was developed to precisely predict the survival rate of ThyC patients. The model was validated based on the most significant DEG GGCT gene expression in ThyC. This model may serve as a guide for the creation of precise treatment plans for ThyC patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12672-023-00772-6. |
format | Online Article Text |
id | pubmed-10501032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-105010322023-09-15 Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes Sun, Wencong Wang, Xinhui Li, Guoqing Ding, Chao Wang, Yichen Su, Zijie Xue, Meifang Discov Oncol Research BACKGROUND: The prevalence of thyroid cancer (ThyC), a frequent malignant tumor of the endocrine system, has been rapidly increasing over time. The mitophagy pathway is reported to play a critical role in ThyC onset and progression in many studies. This research aims to create a mitophagy-related survival prediction model for ThyC patients. METHODS: Genes connected to mitophagy were found in the GeneCards database. The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases provided information on the expression patterns of ThyC-related genes. To identify differentially expressed genes (DEGs), R software was employed. The prognostic significance of each DEG was assessed using the prognostic K-M curve. The prognostic model was built using LASSO, ROC, univariate, and multivariate Cox regression analyses. Finally, a nomogram model was developed to predict the survival outcome of ThyC patients in the clinical setting. RESULTS: Through differential analysis, functional enrichment analysis, and protein–protein interaction (PPI) network analysis, we screened 10 key genes related to mitophagy in ThyC. The risk model was eventually developed using LASSO and Cox regression analyses based on the six DEGs related to mitophagy. An altered expression level of a mitophagy-related prognostic gene, GGCT, was found to be the most significant one, according to the KM survival curve analysis. An immunohistochemical (IHC) investigation revealed that ThyC tissues expressed higher levels of GGCT than normal thyroid tissues. The ROC curve verified the satisfactory performance of the model in survival prediction. Multivariate Cox regression analysis showed that the pathological grade, residual tumor volume, and initial tumor lesion type were significantly linked to the prognosis. Finally, we created a nomogram to predict the overall survival rate of ThyC patients at 3-, 5-, and 7- year time points. CONCLUSION: The nomogram risk prediction model was developed to precisely predict the survival rate of ThyC patients. The model was validated based on the most significant DEG GGCT gene expression in ThyC. This model may serve as a guide for the creation of precise treatment plans for ThyC patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12672-023-00772-6. Springer US 2023-09-14 /pmc/articles/PMC10501032/ /pubmed/37707688 http://dx.doi.org/10.1007/s12672-023-00772-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/) . |
spellingShingle | Research Sun, Wencong Wang, Xinhui Li, Guoqing Ding, Chao Wang, Yichen Su, Zijie Xue, Meifang Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
title | Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
title_full | Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
title_fullStr | Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
title_full_unstemmed | Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
title_short | Development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
title_sort | development of a thyroid cancer prognostic model based on the mitophagy-associated differentially expressed genes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501032/ https://www.ncbi.nlm.nih.gov/pubmed/37707688 http://dx.doi.org/10.1007/s12672-023-00772-6 |
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