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A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients

DNA methylation has been reported as one of the most critical epigenetic aberrations during the tumorigenesis and development of breast cancer (BC). This study explored a novel promoter CpG-based signature for long-term survival prediction of BC patients. We used The Cancer Genome Atlas (TCGA) data...

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Autores principales: Guo, Yang, Mao, Xiaoyun, Qiao, Zhen, Chen, Bo, Jin, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606941/
https://www.ncbi.nlm.nih.gov/pubmed/33194705
http://dx.doi.org/10.3389/fonc.2020.579692
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author Guo, Yang
Mao, Xiaoyun
Qiao, Zhen
Chen, Bo
Jin, Feng
author_facet Guo, Yang
Mao, Xiaoyun
Qiao, Zhen
Chen, Bo
Jin, Feng
author_sort Guo, Yang
collection PubMed
description DNA methylation has been reported as one of the most critical epigenetic aberrations during the tumorigenesis and development of breast cancer (BC). This study explored a novel promoter CpG-based signature for long-term survival prediction of BC patients. We used The Cancer Genome Atlas (TCGA) data as training set, and results were validated in an independent dataset from Gene Expression Omnibus (GEO). First, the differential methylation CpG sites were screened in TCGA dataset, of which the candidate promoter CpG sites were preliminarily identified with the univariate Cox regression analysis and the least absolute shrinkage and selection operator regression analysis. Second, the signature was constructed with stepwise regression analysis and multivariate Cox proportional hazards model, which was validated with the survival analysis of two cohorts each from TCGA and GEO databases. The 10-year receiver operating characteristic curves of risk score presented an area under the curve of over 0.7 for both cohorts. A nomogram was also constructed and released. Moreover, Gene Set Enrichment Analysis was performed to identify the more active pathways in high-risk patients. The CpG sites–target gene correlations and differential methylation regions were further explored. In conclusion, the promoter CpG-based signature exhibited good prognostic prediction efficacy in the long-term overall survival of BC patients.
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spelling pubmed-76069412020-11-13 A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients Guo, Yang Mao, Xiaoyun Qiao, Zhen Chen, Bo Jin, Feng Front Oncol Oncology DNA methylation has been reported as one of the most critical epigenetic aberrations during the tumorigenesis and development of breast cancer (BC). This study explored a novel promoter CpG-based signature for long-term survival prediction of BC patients. We used The Cancer Genome Atlas (TCGA) data as training set, and results were validated in an independent dataset from Gene Expression Omnibus (GEO). First, the differential methylation CpG sites were screened in TCGA dataset, of which the candidate promoter CpG sites were preliminarily identified with the univariate Cox regression analysis and the least absolute shrinkage and selection operator regression analysis. Second, the signature was constructed with stepwise regression analysis and multivariate Cox proportional hazards model, which was validated with the survival analysis of two cohorts each from TCGA and GEO databases. The 10-year receiver operating characteristic curves of risk score presented an area under the curve of over 0.7 for both cohorts. A nomogram was also constructed and released. Moreover, Gene Set Enrichment Analysis was performed to identify the more active pathways in high-risk patients. The CpG sites–target gene correlations and differential methylation regions were further explored. In conclusion, the promoter CpG-based signature exhibited good prognostic prediction efficacy in the long-term overall survival of BC patients. Frontiers Media S.A. 2020-10-20 /pmc/articles/PMC7606941/ /pubmed/33194705 http://dx.doi.org/10.3389/fonc.2020.579692 Text en Copyright © 2020 Guo, Mao, Qiao, Chen and Jin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Guo, Yang
Mao, Xiaoyun
Qiao, Zhen
Chen, Bo
Jin, Feng
A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients
title A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients
title_full A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients
title_fullStr A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients
title_full_unstemmed A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients
title_short A Novel Promoter CpG-Based Signature for Long-Term Survival Prediction of Breast Cancer Patients
title_sort novel promoter cpg-based signature for long-term survival prediction of breast cancer patients
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7606941/
https://www.ncbi.nlm.nih.gov/pubmed/33194705
http://dx.doi.org/10.3389/fonc.2020.579692
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