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Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients

BACKGROUND: microRNAs (miRNAs) are considered promising cancer biomarkers, showing high reliability, sensitivity and stability. Our study aimed to identify associations between whole blood miRNA profiles, presence of circulating tumor cells (CTCs) and clinical outcome in post-operative early breast...

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Autores principales: Alunni-Fabbroni, Marianna, Majunke, Leonie, Trapp, Elisabeth K., Tzschaschel, Marie, Mahner, Sven, Fasching, Peter A., Fehm, Tanja, Schneeweiss, Andreas, Beck, Thomas, Lorenz, Ralf, Friedl, Thomas W. P., Janni, Wolfgang, Rack, Brigitte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802058/
https://www.ncbi.nlm.nih.gov/pubmed/29409452
http://dx.doi.org/10.1186/s12885-018-4020-7
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author Alunni-Fabbroni, Marianna
Majunke, Leonie
Trapp, Elisabeth K.
Tzschaschel, Marie
Mahner, Sven
Fasching, Peter A.
Fehm, Tanja
Schneeweiss, Andreas
Beck, Thomas
Lorenz, Ralf
Friedl, Thomas W. P.
Janni, Wolfgang
Rack, Brigitte
author_facet Alunni-Fabbroni, Marianna
Majunke, Leonie
Trapp, Elisabeth K.
Tzschaschel, Marie
Mahner, Sven
Fasching, Peter A.
Fehm, Tanja
Schneeweiss, Andreas
Beck, Thomas
Lorenz, Ralf
Friedl, Thomas W. P.
Janni, Wolfgang
Rack, Brigitte
author_sort Alunni-Fabbroni, Marianna
collection PubMed
description BACKGROUND: microRNAs (miRNAs) are considered promising cancer biomarkers, showing high reliability, sensitivity and stability. Our study aimed to identify associations between whole blood miRNA profiles, presence of circulating tumor cells (CTCs) and clinical outcome in post-operative early breast cancer patients (EBC) to assess the utility of miRNAs as prognostic markers in this setting. METHOD: A total of 48 post-operative patients, recruited in frame of the SUCCESS A trial, were included in this retrospective study and tested with a panel of 8 miRNAs (miR-10b, −19a, − 21, − 22, −20a, − 127, − 155, −200b). Additional 17 female healthy donors with no previous history of cancer were included in the study as negative controls. Blood samples were collected at different time points (pre-adjuvant therapy, post-adjuvant therapy, 2 years follow up), total RNA was extracted and the relative concentration of each miRNA was measured by quantitative PCR and compared in patients stratified on blood collection time or CTC detection. Furthermore, we compared miRNA profiles of patients, for each time point separately, and healthy donors. CTCs were visualized and quantified with immunocytochemistry analysis. Data were analyzed using non-parametric statistical tests. RESULTS: In our experimental system, miR-19a, miR-22 and miR-127 showed the most promising results, differentiating patients at different time points and from healthy controls, while miR-20a, miR-21 and miR-200b did not show any difference among the different groups. miR-10b and miR-155 were never detectable in our experimental system. With respect to patients’ clinical characteristics, we found a significant correlation between miR-200b and lymph node status and between miR-20a and tumor type. Furthermore, miR-127 correlated with the presence of CTCs. Finally, we found a borderline significance between Progression Free Survival and miR-19a levels. CONCLUSIONS: This pilot study suggests that profiling whole blood miRNAs could help to better stratify post-operative EBC patients without any sign of metastasis to prevent later relapse or metastatic events. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4020-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-58020582018-02-14 Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients Alunni-Fabbroni, Marianna Majunke, Leonie Trapp, Elisabeth K. Tzschaschel, Marie Mahner, Sven Fasching, Peter A. Fehm, Tanja Schneeweiss, Andreas Beck, Thomas Lorenz, Ralf Friedl, Thomas W. P. Janni, Wolfgang Rack, Brigitte BMC Cancer Research Article BACKGROUND: microRNAs (miRNAs) are considered promising cancer biomarkers, showing high reliability, sensitivity and stability. Our study aimed to identify associations between whole blood miRNA profiles, presence of circulating tumor cells (CTCs) and clinical outcome in post-operative early breast cancer patients (EBC) to assess the utility of miRNAs as prognostic markers in this setting. METHOD: A total of 48 post-operative patients, recruited in frame of the SUCCESS A trial, were included in this retrospective study and tested with a panel of 8 miRNAs (miR-10b, −19a, − 21, − 22, −20a, − 127, − 155, −200b). Additional 17 female healthy donors with no previous history of cancer were included in the study as negative controls. Blood samples were collected at different time points (pre-adjuvant therapy, post-adjuvant therapy, 2 years follow up), total RNA was extracted and the relative concentration of each miRNA was measured by quantitative PCR and compared in patients stratified on blood collection time or CTC detection. Furthermore, we compared miRNA profiles of patients, for each time point separately, and healthy donors. CTCs were visualized and quantified with immunocytochemistry analysis. Data were analyzed using non-parametric statistical tests. RESULTS: In our experimental system, miR-19a, miR-22 and miR-127 showed the most promising results, differentiating patients at different time points and from healthy controls, while miR-20a, miR-21 and miR-200b did not show any difference among the different groups. miR-10b and miR-155 were never detectable in our experimental system. With respect to patients’ clinical characteristics, we found a significant correlation between miR-200b and lymph node status and between miR-20a and tumor type. Furthermore, miR-127 correlated with the presence of CTCs. Finally, we found a borderline significance between Progression Free Survival and miR-19a levels. CONCLUSIONS: This pilot study suggests that profiling whole blood miRNAs could help to better stratify post-operative EBC patients without any sign of metastasis to prevent later relapse or metastatic events. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4020-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-06 /pmc/articles/PMC5802058/ /pubmed/29409452 http://dx.doi.org/10.1186/s12885-018-4020-7 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Alunni-Fabbroni, Marianna
Majunke, Leonie
Trapp, Elisabeth K.
Tzschaschel, Marie
Mahner, Sven
Fasching, Peter A.
Fehm, Tanja
Schneeweiss, Andreas
Beck, Thomas
Lorenz, Ralf
Friedl, Thomas W. P.
Janni, Wolfgang
Rack, Brigitte
Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients
title Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients
title_full Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients
title_fullStr Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients
title_full_unstemmed Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients
title_short Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients
title_sort whole blood micrornas as potential biomarkers in post-operative early breast cancer patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5802058/
https://www.ncbi.nlm.nih.gov/pubmed/29409452
http://dx.doi.org/10.1186/s12885-018-4020-7
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