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Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer
BACKGROUND: The clinical benefit of determining the status of HER-2/neu amplification in breast cancer patients is well accepted. Although immunohistochemistry (IHC) is the most frequently used method to assess the over-expression of HER-2 protein, fluorescent in-situ hybridization (FISH) is recogni...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1382241/ https://www.ncbi.nlm.nih.gov/pubmed/16420697 http://dx.doi.org/10.1186/1472-6890-6-2 |
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author | Nistor, Andreea Watson, Peter H Pettigrew, Norman Tabiti, Karim Dawson, Angelika Myal, Yvonne |
author_facet | Nistor, Andreea Watson, Peter H Pettigrew, Norman Tabiti, Karim Dawson, Angelika Myal, Yvonne |
author_sort | Nistor, Andreea |
collection | PubMed |
description | BACKGROUND: The clinical benefit of determining the status of HER-2/neu amplification in breast cancer patients is well accepted. Although immunohistochemistry (IHC) is the most frequently used method to assess the over-expression of HER-2 protein, fluorescent in-situ hybridization (FISH) is recognized as the "gold standard" for the determining of HER-2/neu status. The greatest discordance between the two methods occurs among breast tumors that receive an indeterminate IHC score of 2+. More recently, a real-time polymerase chain reaction (PCR) assay using the LightCycler(® )has been developed for quantifying HER-2/neu gene amplification. In this study, we evaluated the sensitivity and specificity of a commercially available LightCycler assay as it compares to FISH. To determine whether this assay provides an accurate alternative for the determination of HER-2/neu status, we focused primarily on tumors that were deemed indeterminate or borderline status by IHC. METHODS: Thirty-nine breast tumors receiving an IHC score of 2+ were evaluated by both FISH and LightCycler(® )technologies in order to determine whether quantitative real-time PCR provides an accurate alternative for the determination of HER-2/neu status. RESULTS: We found a high concordance (92%) between FISH and real-time PCR results. We also observed that 10% of these tumors were positive for gene amplification by both FISH and real-time PCR. CONCLUSION: The data show that the results obtained for the gene amplification of HER-2/neu by real-time PCR on the LightCycler(® )instrument is comparable to results obtained by FISH. These results therefore suggest that real-time PCR analysis, using the LightCycler(®), is a viable alternative to FISH for reassessing breast tumors which receive an IHC score of 2+, and that a combined IHC and real-time PCR approach for the determination of HER-2 status in breast cancer patients may be an effective and efficient strategy. |
format | Text |
id | pubmed-1382241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-13822412006-02-25 Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer Nistor, Andreea Watson, Peter H Pettigrew, Norman Tabiti, Karim Dawson, Angelika Myal, Yvonne BMC Clin Pathol Research Article BACKGROUND: The clinical benefit of determining the status of HER-2/neu amplification in breast cancer patients is well accepted. Although immunohistochemistry (IHC) is the most frequently used method to assess the over-expression of HER-2 protein, fluorescent in-situ hybridization (FISH) is recognized as the "gold standard" for the determining of HER-2/neu status. The greatest discordance between the two methods occurs among breast tumors that receive an indeterminate IHC score of 2+. More recently, a real-time polymerase chain reaction (PCR) assay using the LightCycler(® )has been developed for quantifying HER-2/neu gene amplification. In this study, we evaluated the sensitivity and specificity of a commercially available LightCycler assay as it compares to FISH. To determine whether this assay provides an accurate alternative for the determination of HER-2/neu status, we focused primarily on tumors that were deemed indeterminate or borderline status by IHC. METHODS: Thirty-nine breast tumors receiving an IHC score of 2+ were evaluated by both FISH and LightCycler(® )technologies in order to determine whether quantitative real-time PCR provides an accurate alternative for the determination of HER-2/neu status. RESULTS: We found a high concordance (92%) between FISH and real-time PCR results. We also observed that 10% of these tumors were positive for gene amplification by both FISH and real-time PCR. CONCLUSION: The data show that the results obtained for the gene amplification of HER-2/neu by real-time PCR on the LightCycler(® )instrument is comparable to results obtained by FISH. These results therefore suggest that real-time PCR analysis, using the LightCycler(®), is a viable alternative to FISH for reassessing breast tumors which receive an IHC score of 2+, and that a combined IHC and real-time PCR approach for the determination of HER-2 status in breast cancer patients may be an effective and efficient strategy. BioMed Central 2006-01-18 /pmc/articles/PMC1382241/ /pubmed/16420697 http://dx.doi.org/10.1186/1472-6890-6-2 Text en Copyright © 2006 Nistor et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Nistor, Andreea Watson, Peter H Pettigrew, Norman Tabiti, Karim Dawson, Angelika Myal, Yvonne Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer |
title | Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer |
title_full | Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer |
title_fullStr | Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer |
title_full_unstemmed | Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer |
title_short | Real-time PCR complements immunohistochemistry in the determination of HER-2/neu status in breast cancer |
title_sort | real-time pcr complements immunohistochemistry in the determination of her-2/neu status in breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1382241/ https://www.ncbi.nlm.nih.gov/pubmed/16420697 http://dx.doi.org/10.1186/1472-6890-6-2 |
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