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Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer

BACKGROUND: Although breast cancer (BC) has a high survival rate, relapse events may occur which ultimately lead to aggressive disease. Circulating cell-free microRNAs (cf-miRNAs) are a promising minimally invasive biomarker with diagnostic and/or prognostic potential. Unfortunately, there is still...

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Autores principales: Gahlawat, Aoife Ward, Fahed, Lavinia, Witte, Tania, Schott, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276748/
https://www.ncbi.nlm.nih.gov/pubmed/35318434
http://dx.doi.org/10.1038/s41416-022-01756-z
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author Gahlawat, Aoife Ward
Fahed, Lavinia
Witte, Tania
Schott, Sarah
author_facet Gahlawat, Aoife Ward
Fahed, Lavinia
Witte, Tania
Schott, Sarah
author_sort Gahlawat, Aoife Ward
collection PubMed
description BACKGROUND: Although breast cancer (BC) has a high survival rate, relapse events may occur which ultimately lead to aggressive disease. Circulating cell-free microRNAs (cf-miRNAs) are a promising minimally invasive biomarker with diagnostic and/or prognostic potential. Unfortunately, there is still no consensus as to a universal cf-miRNA biomarker in BC and there has been no clinical implementation until now. One major limitation is the technical variation with cf-miRNA isolation and specific quantification methods. METHODS: In this study, we assessed the total levels of cf-miRNAs as a potential prognostic marker for BC in 356 plasma samples from 250 BC patients. RESULTS: High levels of cf-miRNAs significantly correlated with unfavourable clinical features including tumour stage, load and the presence of metastasis at diagnosis. With more than 9 years of follow-up, we could show that global cf-miRNA levels significantly correlated with cancer relapse which was confirmed in multivariate cox regression analysis. Finally, for a subset of patients where the serial plasma was available, levels of cf-miRNAs increased in the plasma prior to clinical detection of progressive disease and were massively elevated in patients who died compared to those still alive at the last timepoint of measurement. CONCLUSIONS: This is the first study to suggest that total cf-miRNA levels in the blood can be used as an independent prognostic marker for BC.
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spelling pubmed-92767482022-07-14 Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer Gahlawat, Aoife Ward Fahed, Lavinia Witte, Tania Schott, Sarah Br J Cancer Article BACKGROUND: Although breast cancer (BC) has a high survival rate, relapse events may occur which ultimately lead to aggressive disease. Circulating cell-free microRNAs (cf-miRNAs) are a promising minimally invasive biomarker with diagnostic and/or prognostic potential. Unfortunately, there is still no consensus as to a universal cf-miRNA biomarker in BC and there has been no clinical implementation until now. One major limitation is the technical variation with cf-miRNA isolation and specific quantification methods. METHODS: In this study, we assessed the total levels of cf-miRNAs as a potential prognostic marker for BC in 356 plasma samples from 250 BC patients. RESULTS: High levels of cf-miRNAs significantly correlated with unfavourable clinical features including tumour stage, load and the presence of metastasis at diagnosis. With more than 9 years of follow-up, we could show that global cf-miRNA levels significantly correlated with cancer relapse which was confirmed in multivariate cox regression analysis. Finally, for a subset of patients where the serial plasma was available, levels of cf-miRNAs increased in the plasma prior to clinical detection of progressive disease and were massively elevated in patients who died compared to those still alive at the last timepoint of measurement. CONCLUSIONS: This is the first study to suggest that total cf-miRNA levels in the blood can be used as an independent prognostic marker for BC. Nature Publishing Group UK 2022-03-22 2022-07-01 /pmc/articles/PMC9276748/ /pubmed/35318434 http://dx.doi.org/10.1038/s41416-022-01756-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gahlawat, Aoife Ward
Fahed, Lavinia
Witte, Tania
Schott, Sarah
Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer
title Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer
title_full Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer
title_fullStr Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer
title_full_unstemmed Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer
title_short Total circulating microRNA level as an independent prognostic marker for risk stratification in breast cancer
title_sort total circulating microrna level as an independent prognostic marker for risk stratification in breast cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276748/
https://www.ncbi.nlm.nih.gov/pubmed/35318434
http://dx.doi.org/10.1038/s41416-022-01756-z
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