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Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection
Serum circulating microRNAs (c‐miRNAs) are serving as useful biomarkers for cancer diagnosis. Here, we describe the development of a one‐step branched rolling circle amplification (BRCA) method to measure serum c‐miRNAs levels for early diagnosis of breast cancer. Four c‐miRNAs, c‐miRNA16 (c‐miR‐16)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125458/ https://www.ncbi.nlm.nih.gov/pubmed/29981251 http://dx.doi.org/10.1111/cas.13725 |
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author | Fan, Tingting Mao, Yu Sun, Qinsheng Liu, Feng Lin, Jin‐Shun Liu, Yajie Cui, Junwei Jiang, Yuyang |
author_facet | Fan, Tingting Mao, Yu Sun, Qinsheng Liu, Feng Lin, Jin‐Shun Liu, Yajie Cui, Junwei Jiang, Yuyang |
author_sort | Fan, Tingting |
collection | PubMed |
description | Serum circulating microRNAs (c‐miRNAs) are serving as useful biomarkers for cancer diagnosis. Here, we describe the development of a one‐step branched rolling circle amplification (BRCA) method to measure serum c‐miRNAs levels for early diagnosis of breast cancer. Four c‐miRNAs, c‐miRNA16 (c‐miR‐16), c‐miRNA21 (c‐miR‐21), c‐miRNA155 (c‐miR‐155), and c‐miRNA195 (c‐miR‐195) were isolated from the serum of 49 breast cancer patients (stages I‐IV) and 19 healthy controls, and analyzed using one‐step BRCA. The serum levels of c‐miR16, c‐miR21, c‐miR155, and c‐miR195 were higher (P < 0.0001) in stage I breast cancer patients than healthy controls. These levels were also higher in several breast cancer molecular subtypes (HER‐2 over‐expression, Luminal A, Luminal B, and triple negative breast cancer) than in healthy control subjects. The diagnostic accuracy of c‐miR16, c‐miR21, c‐miR155, and c‐miR195 for early diagnosis of breast cancer was confirmed by receiver operating characteristic (ROC) curve assay. These results show that the BRCA method can be used to measure serum c‐miRNAs levels, and that this method has high accuracy, sensitivity, and specificity. Moreover, both BRCA approach and quantitative real‐time PCR (qRT‐PCR) method show that the serum levels of c‐miR16, c‐miR21, c‐miR155, and c‐miR195 could be used as biomarkers to improve the early diagnosis of breast cancer, and distinguish different breast cancer molecular subtypes. |
format | Online Article Text |
id | pubmed-6125458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61254582018-09-10 Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection Fan, Tingting Mao, Yu Sun, Qinsheng Liu, Feng Lin, Jin‐Shun Liu, Yajie Cui, Junwei Jiang, Yuyang Cancer Sci Original Articles Serum circulating microRNAs (c‐miRNAs) are serving as useful biomarkers for cancer diagnosis. Here, we describe the development of a one‐step branched rolling circle amplification (BRCA) method to measure serum c‐miRNAs levels for early diagnosis of breast cancer. Four c‐miRNAs, c‐miRNA16 (c‐miR‐16), c‐miRNA21 (c‐miR‐21), c‐miRNA155 (c‐miR‐155), and c‐miRNA195 (c‐miR‐195) were isolated from the serum of 49 breast cancer patients (stages I‐IV) and 19 healthy controls, and analyzed using one‐step BRCA. The serum levels of c‐miR16, c‐miR21, c‐miR155, and c‐miR195 were higher (P < 0.0001) in stage I breast cancer patients than healthy controls. These levels were also higher in several breast cancer molecular subtypes (HER‐2 over‐expression, Luminal A, Luminal B, and triple negative breast cancer) than in healthy control subjects. The diagnostic accuracy of c‐miR16, c‐miR21, c‐miR155, and c‐miR195 for early diagnosis of breast cancer was confirmed by receiver operating characteristic (ROC) curve assay. These results show that the BRCA method can be used to measure serum c‐miRNAs levels, and that this method has high accuracy, sensitivity, and specificity. Moreover, both BRCA approach and quantitative real‐time PCR (qRT‐PCR) method show that the serum levels of c‐miR16, c‐miR21, c‐miR155, and c‐miR195 could be used as biomarkers to improve the early diagnosis of breast cancer, and distinguish different breast cancer molecular subtypes. John Wiley and Sons Inc. 2018-08-20 2018-09 /pmc/articles/PMC6125458/ /pubmed/29981251 http://dx.doi.org/10.1111/cas.13725 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Fan, Tingting Mao, Yu Sun, Qinsheng Liu, Feng Lin, Jin‐Shun Liu, Yajie Cui, Junwei Jiang, Yuyang Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection |
title | Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection |
title_full | Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection |
title_fullStr | Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection |
title_full_unstemmed | Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection |
title_short | Branched rolling circle amplification method for measuring serum circulating microRNA levels for early breast cancer detection |
title_sort | branched rolling circle amplification method for measuring serum circulating microrna levels for early breast cancer detection |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6125458/ https://www.ncbi.nlm.nih.gov/pubmed/29981251 http://dx.doi.org/10.1111/cas.13725 |
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