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Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer

BACKGROUND: Breast cancer (BC) has a high incidence and mortality rate in females. Its conventional clinical characteristics are far from accurate for the prediction of individual outcomes. Therefore, we aimed to develop a novel signature to predict the survival of patients with BC. METHODS: We anal...

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Autores principales: He, Menglin, Hu, Cheng, Deng, Jian, Ji, Hui, Tian, Weiqian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487479/
https://www.ncbi.nlm.nih.gov/pubmed/34600547
http://dx.doi.org/10.1186/s12957-021-02409-w
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author He, Menglin
Hu, Cheng
Deng, Jian
Ji, Hui
Tian, Weiqian
author_facet He, Menglin
Hu, Cheng
Deng, Jian
Ji, Hui
Tian, Weiqian
author_sort He, Menglin
collection PubMed
description BACKGROUND: Breast cancer (BC) has a high incidence and mortality rate in females. Its conventional clinical characteristics are far from accurate for the prediction of individual outcomes. Therefore, we aimed to develop a novel signature to predict the survival of patients with BC. METHODS: We analyzed the data of a training cohort from the Cancer Genome Atlas (TCGA) database and a validation cohort from the Gene Expression Omnibus (GEO) database. After the applications of Gene Set Enrichment Analysis (GSEA) and Cox regression analyses, a glycolysis-related signature for predicting the survival of patients with BC was developed; the signature contained AK3, CACNA1H, IL13RA1, NUP43, PGK1, and SDC1. Furthermore, on the basis of expression levels of the six-gene signature, we constructed a risk score formula to classify the patients into high- and low-risk groups. The receiver operating characteristic (ROC) curve and the Kaplan-Meier curve were used to assess the predicted capacity of the model. Later, a nomogram was developed to predict the outcomes of patients with risk score and clinical features over a period of 1, 3, and 5 years. We further used Human Protein Atlas (HPA) database to validate the expressions of the six biomarkers in tumor and sample tissues, which were taken as control. RESULTS: We constructed a six-gene signature to predict the outcomes of patients with BC. The patients in the high-risk group showed poor prognosis than those in the low-risk group. The area under the curve (AUC) values were 0.719 and 0.702, showing that the prediction performance of the signature is acceptable. Additionally, Cox regression analysis revealed that these biomarkers could independently predict the prognosis of BC patients with BC without being affected by clinical factors. The expression levels of all six biomarkers in BC tissues were higher than that in normal tissues; however, AK3 was an exception. CONCLUSION: We developed a six-gene signature to predict the prognosis of patients with BC. Our signature has been proved to have the ability to make an accurate prediction and might be useful in expanding the hypothesis in clinical research.
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spelling pubmed-84874792021-10-04 Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer He, Menglin Hu, Cheng Deng, Jian Ji, Hui Tian, Weiqian World J Surg Oncol Research BACKGROUND: Breast cancer (BC) has a high incidence and mortality rate in females. Its conventional clinical characteristics are far from accurate for the prediction of individual outcomes. Therefore, we aimed to develop a novel signature to predict the survival of patients with BC. METHODS: We analyzed the data of a training cohort from the Cancer Genome Atlas (TCGA) database and a validation cohort from the Gene Expression Omnibus (GEO) database. After the applications of Gene Set Enrichment Analysis (GSEA) and Cox regression analyses, a glycolysis-related signature for predicting the survival of patients with BC was developed; the signature contained AK3, CACNA1H, IL13RA1, NUP43, PGK1, and SDC1. Furthermore, on the basis of expression levels of the six-gene signature, we constructed a risk score formula to classify the patients into high- and low-risk groups. The receiver operating characteristic (ROC) curve and the Kaplan-Meier curve were used to assess the predicted capacity of the model. Later, a nomogram was developed to predict the outcomes of patients with risk score and clinical features over a period of 1, 3, and 5 years. We further used Human Protein Atlas (HPA) database to validate the expressions of the six biomarkers in tumor and sample tissues, which were taken as control. RESULTS: We constructed a six-gene signature to predict the outcomes of patients with BC. The patients in the high-risk group showed poor prognosis than those in the low-risk group. The area under the curve (AUC) values were 0.719 and 0.702, showing that the prediction performance of the signature is acceptable. Additionally, Cox regression analysis revealed that these biomarkers could independently predict the prognosis of BC patients with BC without being affected by clinical factors. The expression levels of all six biomarkers in BC tissues were higher than that in normal tissues; however, AK3 was an exception. CONCLUSION: We developed a six-gene signature to predict the prognosis of patients with BC. Our signature has been proved to have the ability to make an accurate prediction and might be useful in expanding the hypothesis in clinical research. BioMed Central 2021-10-02 /pmc/articles/PMC8487479/ /pubmed/34600547 http://dx.doi.org/10.1186/s12957-021-02409-w Text en © The Author(s) 2021 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
He, Menglin
Hu, Cheng
Deng, Jian
Ji, Hui
Tian, Weiqian
Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
title Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
title_full Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
title_fullStr Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
title_full_unstemmed Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
title_short Identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
title_sort identification of a novel glycolysis-related signature to predict the prognosis of patients with breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487479/
https://www.ncbi.nlm.nih.gov/pubmed/34600547
http://dx.doi.org/10.1186/s12957-021-02409-w
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