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Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers

Disseminated breast tumour cells in sentinel lymph nodes (SNs) were evaluated by quantitative real-time PCR and the sensitivity of this assay was compared to the routine histological analysis. First, several candidate marker genes were tested for their specificity in axillary lymph nodes (ALN) of 50...

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Autores principales: Weigelt, B, Verduijn, P, Bosma, A J, Rutgers, E J, Peterse, H L, van't Veer, L J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409726/
https://www.ncbi.nlm.nih.gov/pubmed/15083181
http://dx.doi.org/10.1038/sj.bjc.6601659
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author Weigelt, B
Verduijn, P
Bosma, A J
Rutgers, E J
Peterse, H L
van't Veer, L J
author_facet Weigelt, B
Verduijn, P
Bosma, A J
Rutgers, E J
Peterse, H L
van't Veer, L J
author_sort Weigelt, B
collection PubMed
description Disseminated breast tumour cells in sentinel lymph nodes (SNs) were evaluated by quantitative real-time PCR and the sensitivity of this assay was compared to the routine histological analysis. First, several candidate marker genes were tested for their specificity in axillary lymph nodes (ALN) of 50 breast cancer patients and 43 women without breast cancer. The marker gene panel selected, designed to detect the mRNA of CK19, p1B, EGP2 and SBEM, was subsequently applied to detect metastases in 70 SNs that were free of metastases as determined by standard histological evaluation. Remarkably, seven negative SNs showed increased marker gene expression, suggesting the presence of (micro) metastases. Four of these seven SNs positive by real-time PCR proved to contain tumour deposits after careful review of the slides or further sectioning of the paraffin-embedded material. In three PCR positive SNs, however, no tumour cells were found by haematoxylin and eosin staining (H&E) and immunohistologically analysis. The quantitative real-time PCR assay with multiple mRNA markers for the detection of disseminated breast cancer cells in SNs thus resulted in an upstaging of SNs containing metastastic disease of 10% compared to the routine histological analysis. The application of this technique may be of clinical relevance, as it is suggested that micrometastatic disease in SNs are associated with further nodal non-SN metastases in breast cancer.
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spelling pubmed-24097262009-09-10 Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers Weigelt, B Verduijn, P Bosma, A J Rutgers, E J Peterse, H L van't Veer, L J Br J Cancer Molecular and Cellular Pathology Disseminated breast tumour cells in sentinel lymph nodes (SNs) were evaluated by quantitative real-time PCR and the sensitivity of this assay was compared to the routine histological analysis. First, several candidate marker genes were tested for their specificity in axillary lymph nodes (ALN) of 50 breast cancer patients and 43 women without breast cancer. The marker gene panel selected, designed to detect the mRNA of CK19, p1B, EGP2 and SBEM, was subsequently applied to detect metastases in 70 SNs that were free of metastases as determined by standard histological evaluation. Remarkably, seven negative SNs showed increased marker gene expression, suggesting the presence of (micro) metastases. Four of these seven SNs positive by real-time PCR proved to contain tumour deposits after careful review of the slides or further sectioning of the paraffin-embedded material. In three PCR positive SNs, however, no tumour cells were found by haematoxylin and eosin staining (H&E) and immunohistologically analysis. The quantitative real-time PCR assay with multiple mRNA markers for the detection of disseminated breast cancer cells in SNs thus resulted in an upstaging of SNs containing metastastic disease of 10% compared to the routine histological analysis. The application of this technique may be of clinical relevance, as it is suggested that micrometastatic disease in SNs are associated with further nodal non-SN metastases in breast cancer. Nature Publishing Group 2004-04-19 2004-03-30 /pmc/articles/PMC2409726/ /pubmed/15083181 http://dx.doi.org/10.1038/sj.bjc.6601659 Text en Copyright © 2004 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 and Cellular Pathology
Weigelt, B
Verduijn, P
Bosma, A J
Rutgers, E J
Peterse, H L
van't Veer, L J
Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers
title Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers
title_full Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers
title_fullStr Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers
title_full_unstemmed Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers
title_short Detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mRNA markers
title_sort detection of metastases in sentinel lymph nodes of breast cancer patients by multiple mrna markers
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2409726/
https://www.ncbi.nlm.nih.gov/pubmed/15083181
http://dx.doi.org/10.1038/sj.bjc.6601659
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