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DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection

INTRODUCTION: Nipple fluid aspiration provides direct non-invasive sampling of fluid from the mammary ductal system, where the majority of breast cancers originate. DNA promoter hypermethylation (“methylation”) occurs early and at high frequency in breast carcinogenesis, bearing the potential as a b...

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Autores principales: de Groot, Jolien S., Moelans, Cathy B., Elias, Sjoerd G., Fackler, Mary Jo, van Domselaar, Robert, Suijkerbuijk, Karijn P.M., Witkamp, Arjen J., Sukumar, Saraswati, van Diest, Paul J., van der Wall, Elsken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029741/
https://www.ncbi.nlm.nih.gov/pubmed/27028854
http://dx.doi.org/10.18632/oncotarget.8352
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author de Groot, Jolien S.
Moelans, Cathy B.
Elias, Sjoerd G.
Fackler, Mary Jo
van Domselaar, Robert
Suijkerbuijk, Karijn P.M.
Witkamp, Arjen J.
Sukumar, Saraswati
van Diest, Paul J.
van der Wall, Elsken
author_facet de Groot, Jolien S.
Moelans, Cathy B.
Elias, Sjoerd G.
Fackler, Mary Jo
van Domselaar, Robert
Suijkerbuijk, Karijn P.M.
Witkamp, Arjen J.
Sukumar, Saraswati
van Diest, Paul J.
van der Wall, Elsken
author_sort de Groot, Jolien S.
collection PubMed
description INTRODUCTION: Nipple fluid aspiration provides direct non-invasive sampling of fluid from the mammary ductal system, where the majority of breast cancers originate. DNA promoter hypermethylation (“methylation”) occurs early and at high frequency in breast carcinogenesis, bearing the potential as a biomarker for cancer detection at its earliest stages. We assessed methylation in nipple fluid from breasts of healthy women, of women with sporadic breast cancer and of their contralateral breasts. Our goal was to investigate whether nipple fluid can be used as a reliable methylation biomarker source. METHODS: Methylation levels of 13 genes were analysed by quantitative multiplex-methylation specific PCR (QM-MSP) in nipple fluid samples from breasts of healthy women, and from the affected and contralateral breasts of breast cancer patients. RESULTS: Methylation analysis of the low-volume nipple fluid samples was feasible. Despite the generally low methylation levels, cancerous and healthy breasts nipple fluid could be discriminated with an area under the receiver operating characteristic curve (AUC) of 0.64 (p<0.01) based on a multivariate model including AKR1B1, ALX1, RASSF1A and TM6SF1. Within-patient differences between cancerous and contralateral nipple fluid samples were less prominent. CONCLUSIONS: Cancerous nipple fluid contains increased levels of methylation of tumor suppressor genes that potentially could serve as a biomarker for early breast cancer detection.
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spelling pubmed-50297412016-09-29 DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection de Groot, Jolien S. Moelans, Cathy B. Elias, Sjoerd G. Fackler, Mary Jo van Domselaar, Robert Suijkerbuijk, Karijn P.M. Witkamp, Arjen J. Sukumar, Saraswati van Diest, Paul J. van der Wall, Elsken Oncotarget Research Paper INTRODUCTION: Nipple fluid aspiration provides direct non-invasive sampling of fluid from the mammary ductal system, where the majority of breast cancers originate. DNA promoter hypermethylation (“methylation”) occurs early and at high frequency in breast carcinogenesis, bearing the potential as a biomarker for cancer detection at its earliest stages. We assessed methylation in nipple fluid from breasts of healthy women, of women with sporadic breast cancer and of their contralateral breasts. Our goal was to investigate whether nipple fluid can be used as a reliable methylation biomarker source. METHODS: Methylation levels of 13 genes were analysed by quantitative multiplex-methylation specific PCR (QM-MSP) in nipple fluid samples from breasts of healthy women, and from the affected and contralateral breasts of breast cancer patients. RESULTS: Methylation analysis of the low-volume nipple fluid samples was feasible. Despite the generally low methylation levels, cancerous and healthy breasts nipple fluid could be discriminated with an area under the receiver operating characteristic curve (AUC) of 0.64 (p<0.01) based on a multivariate model including AKR1B1, ALX1, RASSF1A and TM6SF1. Within-patient differences between cancerous and contralateral nipple fluid samples were less prominent. CONCLUSIONS: Cancerous nipple fluid contains increased levels of methylation of tumor suppressor genes that potentially could serve as a biomarker for early breast cancer detection. Impact Journals LLC 2016-03-25 /pmc/articles/PMC5029741/ /pubmed/27028854 http://dx.doi.org/10.18632/oncotarget.8352 Text en Copyright: © 2016 de Groot et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
de Groot, Jolien S.
Moelans, Cathy B.
Elias, Sjoerd G.
Fackler, Mary Jo
van Domselaar, Robert
Suijkerbuijk, Karijn P.M.
Witkamp, Arjen J.
Sukumar, Saraswati
van Diest, Paul J.
van der Wall, Elsken
DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
title DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
title_full DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
title_fullStr DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
title_full_unstemmed DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
title_short DNA promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
title_sort dna promoter hypermethylation in nipple fluid: a potential tool for early breast cancer detection
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5029741/
https://www.ncbi.nlm.nih.gov/pubmed/27028854
http://dx.doi.org/10.18632/oncotarget.8352
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