Cargando…

Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer

PURPOSE: Novel noninvasive biomarkers with high sensitivity and specificity for the diagnosis of breast cancer (BC) are urgently needed in clinics. The aim of this study was to explore whether miRNAs from the miR-106a–363 cluster can be detected in the circulation of BC patients and whether these mi...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Minghui, Zhou, Yan, Xia, Tiansong, Zhou, Xin, Huang, Zebo, Zhang, Huo, Zhu, Wei, Ding, Qiang, Wang, Shui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999170/
https://www.ncbi.nlm.nih.gov/pubmed/29557526
http://dx.doi.org/10.1007/s10549-018-4757-3
_version_ 1783331377595285504
author Li, Minghui
Zhou, Yan
Xia, Tiansong
Zhou, Xin
Huang, Zebo
Zhang, Huo
Zhu, Wei
Ding, Qiang
Wang, Shui
author_facet Li, Minghui
Zhou, Yan
Xia, Tiansong
Zhou, Xin
Huang, Zebo
Zhang, Huo
Zhu, Wei
Ding, Qiang
Wang, Shui
author_sort Li, Minghui
collection PubMed
description PURPOSE: Novel noninvasive biomarkers with high sensitivity and specificity for the diagnosis of breast cancer (BC) are urgently needed in clinics. The aim of this study was to explore whether miRNAs from the miR-106a–363 cluster can be detected in the circulation of BC patients and whether these miRNAs can serve as potential diagnostic biomarkers. METHODS: The expression of 12 miRNAs from the miR-106a–363 cluster was evaluated using qRT-PCR in 400 plasma samples (from 200 BC patients and 200 healthy controls (HCs)) and 406 serum samples (from 204 BC patients and 202 HCs) via a three-phase study. The identified miRNAs were further examined in tissues (32 paired breast tissues), plasma exosomes (from 32 BC patients and 32 HCs), and serum exosomes (from 32 BC patients and 32 HCs). RESULTS: Upregulated levels of four plasma miRNAs (miR-106a-3p, miR-106a-5p, miR-20b-5p, and miR-92a-2-5p) and four serum miRNAs (miR-106a-5p, miR-19b-3p, miR-20b-5p, and miR-92a-3p) were identified and validated in BC. A plasma 4-miRNA panel and a serum 4-miRNA panel were constructed to discriminate BC patients from HCs. The areas under the receiver-operating characteristic curves of the plasma panel were 0.880, 0.902, and 0.858, and those of the serum panel were 0.910, 0.974, and 0.949 for the training, testing, and external validation phases, respectively. Two overlapping miRNAs (miR-106a-5p and miR-20b-5p) were consistently upregulated in BC tissues. Except for the expression of the plasma-derived exosomal miR-20b-5p, the expression patterns of exosomal miRNAs were concordant between plasma and serum, indicating the potential use of exosomal miRNAs as biomarkers. CONCLUSION: We identified four plasma miRNAs and four serum miRNAs from the miR-106a–363 cluster as promising novel biomarkers for the diagnosis of BC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10549-018-4757-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5999170
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-59991702018-06-28 Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer Li, Minghui Zhou, Yan Xia, Tiansong Zhou, Xin Huang, Zebo Zhang, Huo Zhu, Wei Ding, Qiang Wang, Shui Breast Cancer Res Treat Preclinical Study PURPOSE: Novel noninvasive biomarkers with high sensitivity and specificity for the diagnosis of breast cancer (BC) are urgently needed in clinics. The aim of this study was to explore whether miRNAs from the miR-106a–363 cluster can be detected in the circulation of BC patients and whether these miRNAs can serve as potential diagnostic biomarkers. METHODS: The expression of 12 miRNAs from the miR-106a–363 cluster was evaluated using qRT-PCR in 400 plasma samples (from 200 BC patients and 200 healthy controls (HCs)) and 406 serum samples (from 204 BC patients and 202 HCs) via a three-phase study. The identified miRNAs were further examined in tissues (32 paired breast tissues), plasma exosomes (from 32 BC patients and 32 HCs), and serum exosomes (from 32 BC patients and 32 HCs). RESULTS: Upregulated levels of four plasma miRNAs (miR-106a-3p, miR-106a-5p, miR-20b-5p, and miR-92a-2-5p) and four serum miRNAs (miR-106a-5p, miR-19b-3p, miR-20b-5p, and miR-92a-3p) were identified and validated in BC. A plasma 4-miRNA panel and a serum 4-miRNA panel were constructed to discriminate BC patients from HCs. The areas under the receiver-operating characteristic curves of the plasma panel were 0.880, 0.902, and 0.858, and those of the serum panel were 0.910, 0.974, and 0.949 for the training, testing, and external validation phases, respectively. Two overlapping miRNAs (miR-106a-5p and miR-20b-5p) were consistently upregulated in BC tissues. Except for the expression of the plasma-derived exosomal miR-20b-5p, the expression patterns of exosomal miRNAs were concordant between plasma and serum, indicating the potential use of exosomal miRNAs as biomarkers. CONCLUSION: We identified four plasma miRNAs and four serum miRNAs from the miR-106a–363 cluster as promising novel biomarkers for the diagnosis of BC. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10549-018-4757-3) contains supplementary material, which is available to authorized users. Springer US 2018-03-20 2018 /pmc/articles/PMC5999170/ /pubmed/29557526 http://dx.doi.org/10.1007/s10549-018-4757-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Preclinical Study
Li, Minghui
Zhou, Yan
Xia, Tiansong
Zhou, Xin
Huang, Zebo
Zhang, Huo
Zhu, Wei
Ding, Qiang
Wang, Shui
Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer
title Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer
title_full Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer
title_fullStr Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer
title_full_unstemmed Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer
title_short Circulating microRNAs from the miR-106a–363 cluster on chromosome X as novel diagnostic biomarkers for breast cancer
title_sort circulating micrornas from the mir-106a–363 cluster on chromosome x as novel diagnostic biomarkers for breast cancer
topic Preclinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999170/
https://www.ncbi.nlm.nih.gov/pubmed/29557526
http://dx.doi.org/10.1007/s10549-018-4757-3
work_keys_str_mv AT liminghui circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT zhouyan circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT xiatiansong circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT zhouxin circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT huangzebo circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT zhanghuo circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT zhuwei circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT dingqiang circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer
AT wangshui circulatingmicrornasfromthemir106a363clusteronchromosomexasnoveldiagnosticbiomarkersforbreastcancer