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Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer

Breast cancer is one of the most malignant diseases in women worldwide. Serum microRNAs (miRNAs), with the characteristics of high sensitivity and specificity, have recently attracted more attentions to serve as potential biomarkers for tumor diseases. In this study, 194 breast cancer patients’ seru...

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Autores principales: Guo, Jian, Liu, Chen, Wang, Wei, Liu, Yan, He, Huiwen, Chen, Chong, Xiang, Rong, Luo, Yunping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062026/
https://www.ncbi.nlm.nih.gov/pubmed/30048472
http://dx.doi.org/10.1371/journal.pone.0200716
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author Guo, Jian
Liu, Chen
Wang, Wei
Liu, Yan
He, Huiwen
Chen, Chong
Xiang, Rong
Luo, Yunping
author_facet Guo, Jian
Liu, Chen
Wang, Wei
Liu, Yan
He, Huiwen
Chen, Chong
Xiang, Rong
Luo, Yunping
author_sort Guo, Jian
collection PubMed
description Breast cancer is one of the most malignant diseases in women worldwide. Serum microRNAs (miRNAs), with the characteristics of high sensitivity and specificity, have recently attracted more attentions to serve as potential biomarkers for tumor diseases. In this study, 194 breast cancer patients’ serum samples were collected before surgery and enrolled into different groups based on their diagnostic information. To search for breast cancer diagnostic biomarkers, serum miRNAs were screened by microarray in pooled samples of healthy volunteers and breast cancer patients in different clinical stages. The miRNAs were further verified in each individual patient’s serum samples in diagnostic and predictive sets. The serum level of miR-1915-3p was upregulated and miR-455-3p was downregulated significantly in breast cancer patients compared with healthy volunteers. Furthermore, the patients with infiltrating carcinoma or lymph node metastasis had a higher serum level of miR-1915-3p and lower serum level of miR-455-3p than patients with the carcinoma in situ or patients without lymph node metastasis. ROC analysis suggested that miR-1915-3p and miR-455-3p had the potential as a promising serum diagnostic and predictive biomarkers of breast cancer. miR-1915-3p was over-expressed in certain human breast cancer cells. Functional experiments in vitro showed that miR-1915-3p enhanced cell proliferative and migrational abilities. Overexpression of miR-1915-3p repressed target gene DUSP3 and activated ERK1/2. Collectively, this study provided a new insight that miR-1915-3p might play a role in the development of breast cancer and that serum miR-1915-3p and miR-455-3p could serve as diagnostic and predictive biomarkers for breast cancer.
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spelling pubmed-60620262018-08-03 Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer Guo, Jian Liu, Chen Wang, Wei Liu, Yan He, Huiwen Chen, Chong Xiang, Rong Luo, Yunping PLoS One Research Article Breast cancer is one of the most malignant diseases in women worldwide. Serum microRNAs (miRNAs), with the characteristics of high sensitivity and specificity, have recently attracted more attentions to serve as potential biomarkers for tumor diseases. In this study, 194 breast cancer patients’ serum samples were collected before surgery and enrolled into different groups based on their diagnostic information. To search for breast cancer diagnostic biomarkers, serum miRNAs were screened by microarray in pooled samples of healthy volunteers and breast cancer patients in different clinical stages. The miRNAs were further verified in each individual patient’s serum samples in diagnostic and predictive sets. The serum level of miR-1915-3p was upregulated and miR-455-3p was downregulated significantly in breast cancer patients compared with healthy volunteers. Furthermore, the patients with infiltrating carcinoma or lymph node metastasis had a higher serum level of miR-1915-3p and lower serum level of miR-455-3p than patients with the carcinoma in situ or patients without lymph node metastasis. ROC analysis suggested that miR-1915-3p and miR-455-3p had the potential as a promising serum diagnostic and predictive biomarkers of breast cancer. miR-1915-3p was over-expressed in certain human breast cancer cells. Functional experiments in vitro showed that miR-1915-3p enhanced cell proliferative and migrational abilities. Overexpression of miR-1915-3p repressed target gene DUSP3 and activated ERK1/2. Collectively, this study provided a new insight that miR-1915-3p might play a role in the development of breast cancer and that serum miR-1915-3p and miR-455-3p could serve as diagnostic and predictive biomarkers for breast cancer. Public Library of Science 2018-07-26 /pmc/articles/PMC6062026/ /pubmed/30048472 http://dx.doi.org/10.1371/journal.pone.0200716 Text en © 2018 Guo 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, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Guo, Jian
Liu, Chen
Wang, Wei
Liu, Yan
He, Huiwen
Chen, Chong
Xiang, Rong
Luo, Yunping
Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer
title Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer
title_full Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer
title_fullStr Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer
title_full_unstemmed Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer
title_short Identification of serum miR-1915-3p and miR-455-3p as biomarkers for breast cancer
title_sort identification of serum mir-1915-3p and mir-455-3p as biomarkers for breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6062026/
https://www.ncbi.nlm.nih.gov/pubmed/30048472
http://dx.doi.org/10.1371/journal.pone.0200716
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