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Breast cancer identification via modeling of peripherally circulating miRNAs

Prolonged life expectancy in humans has been accompanied by an increase in the prevalence of cancers. Breast cancer (BC) is the leading cause of cancer-related deaths. It accounts for one-fourth of all diagnosed cancers and affects one in eight females worldwide. Given the high BC prevalence, there...

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Autores principales: Cui, Xiaomeng, Li, Zhangming, Zhao, Yilei, Song, Anqi, Shi, Yunbo, Hai, Xin, Zhu, Wenliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875392/
https://www.ncbi.nlm.nih.gov/pubmed/29607263
http://dx.doi.org/10.7717/peerj.4551
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author Cui, Xiaomeng
Li, Zhangming
Zhao, Yilei
Song, Anqi
Shi, Yunbo
Hai, Xin
Zhu, Wenliang
author_facet Cui, Xiaomeng
Li, Zhangming
Zhao, Yilei
Song, Anqi
Shi, Yunbo
Hai, Xin
Zhu, Wenliang
author_sort Cui, Xiaomeng
collection PubMed
description Prolonged life expectancy in humans has been accompanied by an increase in the prevalence of cancers. Breast cancer (BC) is the leading cause of cancer-related deaths. It accounts for one-fourth of all diagnosed cancers and affects one in eight females worldwide. Given the high BC prevalence, there is a practical need for demographic screening of the disease. In the present study, we re-analyzed a large microRNA (miRNA) expression dataset (GSE73002), with the goal of optimizing miRNA biomarker selection using neural network cascade (NNC) modeling. Our results identified numerous candidate miRNA biomarkers that are technically suitable for BC detection. We combined three miRNAs (miR-1246, miR-6756-5p, and miR-8073) into a single panel to generate an NNC model, which successfully detected BC with 97.1% accuracy in an independent validation cohort comprising 429 BC patients and 895 healthy controls. In contrast, at least seven miRNAs were merged in a multiple linear regression model to obtain equivalent diagnostic performance (96.4% accuracy in the independent validation set). Our findings suggested that suitable modeling can effectively reduce the number of miRNAs required in a biomarker panel without compromising prediction accuracy, thereby increasing the technical possibility of early detection of BC.
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spelling pubmed-58753922018-03-30 Breast cancer identification via modeling of peripherally circulating miRNAs Cui, Xiaomeng Li, Zhangming Zhao, Yilei Song, Anqi Shi, Yunbo Hai, Xin Zhu, Wenliang PeerJ Oncology Prolonged life expectancy in humans has been accompanied by an increase in the prevalence of cancers. Breast cancer (BC) is the leading cause of cancer-related deaths. It accounts for one-fourth of all diagnosed cancers and affects one in eight females worldwide. Given the high BC prevalence, there is a practical need for demographic screening of the disease. In the present study, we re-analyzed a large microRNA (miRNA) expression dataset (GSE73002), with the goal of optimizing miRNA biomarker selection using neural network cascade (NNC) modeling. Our results identified numerous candidate miRNA biomarkers that are technically suitable for BC detection. We combined three miRNAs (miR-1246, miR-6756-5p, and miR-8073) into a single panel to generate an NNC model, which successfully detected BC with 97.1% accuracy in an independent validation cohort comprising 429 BC patients and 895 healthy controls. In contrast, at least seven miRNAs were merged in a multiple linear regression model to obtain equivalent diagnostic performance (96.4% accuracy in the independent validation set). Our findings suggested that suitable modeling can effectively reduce the number of miRNAs required in a biomarker panel without compromising prediction accuracy, thereby increasing the technical possibility of early detection of BC. PeerJ Inc. 2018-03-26 /pmc/articles/PMC5875392/ /pubmed/29607263 http://dx.doi.org/10.7717/peerj.4551 Text en ©2018 Cui et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Oncology
Cui, Xiaomeng
Li, Zhangming
Zhao, Yilei
Song, Anqi
Shi, Yunbo
Hai, Xin
Zhu, Wenliang
Breast cancer identification via modeling of peripherally circulating miRNAs
title Breast cancer identification via modeling of peripherally circulating miRNAs
title_full Breast cancer identification via modeling of peripherally circulating miRNAs
title_fullStr Breast cancer identification via modeling of peripherally circulating miRNAs
title_full_unstemmed Breast cancer identification via modeling of peripherally circulating miRNAs
title_short Breast cancer identification via modeling of peripherally circulating miRNAs
title_sort breast cancer identification via modeling of peripherally circulating mirnas
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875392/
https://www.ncbi.nlm.nih.gov/pubmed/29607263
http://dx.doi.org/10.7717/peerj.4551
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