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Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer
BACKGROUND: Thyroid cancer (THCA) is one of the most commonly malignant endocrine tumors worldwide. This study aimed to explore new gene signatures to better predict the metastasis and survival rate of patients with THCA. METHODS: mRNA transcriptome date and clinical characteristics of THCA were obt...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248573/ https://www.ncbi.nlm.nih.gov/pubmed/37304543 http://dx.doi.org/10.21037/tcr-22-2548 |
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author | Wang, Bo Zhu, Yongqian Zhang, Xiang Wang, Zijie |
author_facet | Wang, Bo Zhu, Yongqian Zhang, Xiang Wang, Zijie |
author_sort | Wang, Bo |
collection | PubMed |
description | BACKGROUND: Thyroid cancer (THCA) is one of the most commonly malignant endocrine tumors worldwide. This study aimed to explore new gene signatures to better predict the metastasis and survival rate of patients with THCA. METHODS: mRNA transcriptome date and clinical characteristics of THCA were obtained from the Cancer Genome Atlas (TCGA) database to identify the expression and prognostic implications of glycolysis-related genes. Gene Set Enrichment Analysis (GSEA) of differentiated expressed genes was performed, and relationship between genes and glycolysis was observed in the Cox proportional regression model. Using the cBioPortal, mutations were subsequently identified in model genes. RESULTS: A 3-gene (HSPA5, KIF20A and SDC2) signature based on glycolysis related genes was identified and used to predict metastasis and survival rate in patients with THCA. Further expression analysis revealed that KIF20A was a poor prognostic gene, while HSPA5 and SDC2 were good prognostic genes. Evaluating the prognosis of patients with THCA could be more effective with this model. CONCLUSIONS: The study reported a three-gene signature of THCA, including HSPA5, KIF20A and SDC2, which were found to be closely correlated with the glycolysis of THCA, and it showed a high efficacy to the prediction of metastasis and survival rate of THCA. |
format | Online Article Text |
id | pubmed-10248573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-102485732023-06-09 Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer Wang, Bo Zhu, Yongqian Zhang, Xiang Wang, Zijie Transl Cancer Res Original Article BACKGROUND: Thyroid cancer (THCA) is one of the most commonly malignant endocrine tumors worldwide. This study aimed to explore new gene signatures to better predict the metastasis and survival rate of patients with THCA. METHODS: mRNA transcriptome date and clinical characteristics of THCA were obtained from the Cancer Genome Atlas (TCGA) database to identify the expression and prognostic implications of glycolysis-related genes. Gene Set Enrichment Analysis (GSEA) of differentiated expressed genes was performed, and relationship between genes and glycolysis was observed in the Cox proportional regression model. Using the cBioPortal, mutations were subsequently identified in model genes. RESULTS: A 3-gene (HSPA5, KIF20A and SDC2) signature based on glycolysis related genes was identified and used to predict metastasis and survival rate in patients with THCA. Further expression analysis revealed that KIF20A was a poor prognostic gene, while HSPA5 and SDC2 were good prognostic genes. Evaluating the prognosis of patients with THCA could be more effective with this model. CONCLUSIONS: The study reported a three-gene signature of THCA, including HSPA5, KIF20A and SDC2, which were found to be closely correlated with the glycolysis of THCA, and it showed a high efficacy to the prediction of metastasis and survival rate of THCA. AME Publishing Company 2023-05-12 2023-05-31 /pmc/articles/PMC10248573/ /pubmed/37304543 http://dx.doi.org/10.21037/tcr-22-2548 Text en 2023 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Wang, Bo Zhu, Yongqian Zhang, Xiang Wang, Zijie Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
title | Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
title_full | Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
title_fullStr | Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
title_full_unstemmed | Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
title_short | Identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
title_sort | identification and validation of a glycolysis-related gene signature for predicting metastasis and survival rate in patients with thyroid cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10248573/ https://www.ncbi.nlm.nih.gov/pubmed/37304543 http://dx.doi.org/10.21037/tcr-22-2548 |
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