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Detection of HER2 amplification in circulating free DNA in patients with breast cancer

BACKGROUND: Human epidermal growth factor receptor 2 (HER2) is amplified and overexpressed in 20–25% of breast cancers. This study investigated circulating free DNA (cfDNA) for detection of HER2 gene amplification in patients with breast cancer. METHODS: Circulating free DNA was extracted from plasm...

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Autores principales: Page, K, Hava, N, Ward, B, Brown, J, Guttery, D S, Ruangpratheep, C, Blighe, K, Sharma, A, Walker, R A, Coombes, R C, Shaw, J A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078598/
https://www.ncbi.nlm.nih.gov/pubmed/21427727
http://dx.doi.org/10.1038/bjc.2011.89
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author Page, K
Hava, N
Ward, B
Brown, J
Guttery, D S
Ruangpratheep, C
Blighe, K
Sharma, A
Walker, R A
Coombes, R C
Shaw, J A
author_facet Page, K
Hava, N
Ward, B
Brown, J
Guttery, D S
Ruangpratheep, C
Blighe, K
Sharma, A
Walker, R A
Coombes, R C
Shaw, J A
author_sort Page, K
collection PubMed
description BACKGROUND: Human epidermal growth factor receptor 2 (HER2) is amplified and overexpressed in 20–25% of breast cancers. This study investigated circulating free DNA (cfDNA) for detection of HER2 gene amplification in patients with breast cancer. METHODS: Circulating free DNA was extracted from plasma of unselected patients with primary breast cancer (22 before surgery and 68 following treatment), 30 metastatic patients and 98 female controls using the QIAamp Blood DNA Mini Kit (Qiagen). The ratio of HER2 to an unamplified reference gene (contactin-associated protein 1 (CNTNAP1)) was measured in cfDNA samples by quantitative PCR (qPCR) using SK-BR-3 cell line DNA as a positive control. RESULTS: We validated the qPCR assay with DNA extracted from 23 HER2 3+ and 40 HER2-negative tumour tissue samples; the results agreed for 60 of 63 (95.2%) tumours. Amplification was detected in cfDNA for 8 of 68 patients following primary breast cancer treatment and 5 of 30 metastatic patients, but was undetected in 22 patients with primary breast cancer and 98 healthy female controls. Of the patients with amplification in cfDNA, 10 had HER2 3+ tumour status by immunohistochemistry. CONCLUSIONS: The results demonstrate for the first time the existence of amplified HER2 in cfDNA in the follow-up of breast cancer patients who are otherwise disease free. This approach could potentially provide a marker in patients with HER2-positive breast cancer.
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spelling pubmed-30785982012-04-12 Detection of HER2 amplification in circulating free DNA in patients with breast cancer Page, K Hava, N Ward, B Brown, J Guttery, D S Ruangpratheep, C Blighe, K Sharma, A Walker, R A Coombes, R C Shaw, J A Br J Cancer Molecular Diagnostics BACKGROUND: Human epidermal growth factor receptor 2 (HER2) is amplified and overexpressed in 20–25% of breast cancers. This study investigated circulating free DNA (cfDNA) for detection of HER2 gene amplification in patients with breast cancer. METHODS: Circulating free DNA was extracted from plasma of unselected patients with primary breast cancer (22 before surgery and 68 following treatment), 30 metastatic patients and 98 female controls using the QIAamp Blood DNA Mini Kit (Qiagen). The ratio of HER2 to an unamplified reference gene (contactin-associated protein 1 (CNTNAP1)) was measured in cfDNA samples by quantitative PCR (qPCR) using SK-BR-3 cell line DNA as a positive control. RESULTS: We validated the qPCR assay with DNA extracted from 23 HER2 3+ and 40 HER2-negative tumour tissue samples; the results agreed for 60 of 63 (95.2%) tumours. Amplification was detected in cfDNA for 8 of 68 patients following primary breast cancer treatment and 5 of 30 metastatic patients, but was undetected in 22 patients with primary breast cancer and 98 healthy female controls. Of the patients with amplification in cfDNA, 10 had HER2 3+ tumour status by immunohistochemistry. CONCLUSIONS: The results demonstrate for the first time the existence of amplified HER2 in cfDNA in the follow-up of breast cancer patients who are otherwise disease free. This approach could potentially provide a marker in patients with HER2-positive breast cancer. Nature Publishing Group 2011-04-12 2011-03-22 /pmc/articles/PMC3078598/ /pubmed/21427727 http://dx.doi.org/10.1038/bjc.2011.89 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license 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 license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Page, K
Hava, N
Ward, B
Brown, J
Guttery, D S
Ruangpratheep, C
Blighe, K
Sharma, A
Walker, R A
Coombes, R C
Shaw, J A
Detection of HER2 amplification in circulating free DNA in patients with breast cancer
title Detection of HER2 amplification in circulating free DNA in patients with breast cancer
title_full Detection of HER2 amplification in circulating free DNA in patients with breast cancer
title_fullStr Detection of HER2 amplification in circulating free DNA in patients with breast cancer
title_full_unstemmed Detection of HER2 amplification in circulating free DNA in patients with breast cancer
title_short Detection of HER2 amplification in circulating free DNA in patients with breast cancer
title_sort detection of her2 amplification in circulating free dna in patients with breast cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3078598/
https://www.ncbi.nlm.nih.gov/pubmed/21427727
http://dx.doi.org/10.1038/bjc.2011.89
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