Real-Time RT-PCR Analysis for Evaluating the Her2/neu Status in Breast Cancer

被引:27
作者
Cuadros, M. [1 ,3 ]
Talavera, P. [3 ]
Lopez, F. J. [1 ]
Garcia-Perez, I. [2 ]
Blanco, A. [1 ]
Concha, A. [2 ,3 ]
机构
[1] Univ Granada, Dept Computat Sci & Artificial Intelligence, ES-18071 Granada, Spain
[2] Hosp Univ Virgen Nieves, Dept Pathol, Granada, Spain
[3] Hosp Univ Virgen Nieves, Tissue & Tumor Bank, Dept Pathol, Granada, Spain
关键词
Immunohistochemistry; In situ hybridization; Fluorescence; Quantitative RT-PCR; mRNA quantification; Breast cancer; c-erbB2; Her2/neu; IN-SITU HYBRIDIZATION; REVERSE TRANSCRIPTION-PCR; NEU ONCOGENE; GENE AMPLIFICATION; QUANTITATIVE PCR; OVEREXPRESSION; FISH; CARCINOMAS; IMMUNOHISTOCHEMISTRY; EXPRESSION;
D O I
10.1159/000272953
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: The Her2/neu status is of great clinical value in breast tumor patients. Fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) techniques are the test of choice for many practicing pathologies. The main objective of this retrospective study was to investigate the relationship between Her2/neu breast cancer amplification and overexpression (DNA, mRNA and protein). Methods: To accomplish this goal, we evaluated Her2/neu mRNA expression by real-time quantitative RT-PCR, gene amplification by FISH and protein expression by IHC. Results: An excellent correlation between FISH and IHC Her2/neu results was observed, confirming that protein levels were directly related to DNA amplification. Polysomy 17 was frequently found in tumors showing Her2/neu overexpression. However, we did not find any statistically significant correlation among DNA, mRNA and protein levels, suggesting that Her2/neu could be post-transcriptionally regulated. Conclusions: There was a high agreement between Her2/neu gene amplification and protein overexpression but not mRNA expression levels. Nevertheless, IHC3+ and FISH-positive tumors indicated higher expression levels of Her2/neu mRNA by RT-PCR than those observed in IHC and FISH-negative tumors. These findings question the relevance of quantitative RT-PCR in routine assessment of Her2/neu overexpression in human breast cancer in the clinical laboratory setting. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:38 / 45
页数:8
相关论文
共 33 条
[1]  
[Anonymous], 2008, SCIENCEDAILY
[2]   Quantitative PCR and HER2 testing in breast cancer [J].
Barberis, Massimo ;
Pellegrini, Caterina ;
Cannone, Maria ;
Arizzi, Carmelo ;
Coggi, Guido ;
Bosari, Silvano .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2008, 129 (04) :563-570
[3]  
Bartanusz V, 2003, Swiss Surg, V9, P55, DOI 10.1024/1023-9332.9.2.55
[4]   Quantitative real-time PCR analysis and microarray-based RNA expression of HER2 in relation to outcome [J].
Bergqvist, J. ;
Ohd, J. F. ;
Smeds, J. ;
Klaar, S. ;
Isola, J. ;
Nordgren, H. ;
Elmberger, G. P. ;
Hellborg, H. ;
Bjohle, J. ;
Borg, A.-L. ;
Skoog, L. ;
Bergh, J. .
ANNALS OF ONCOLOGY, 2007, 18 (05) :845-850
[5]   Current perspectives on HER2 testing:: A review of national testing guidelines [J].
Bilous, M ;
Dowsett, M ;
Hanna, W ;
Isola, J ;
Lebeau, A ;
Moreno, A ;
Penault-Llorca, F ;
Rüschoff, J ;
Tomasic, G ;
de Vijver, MV .
MODERN PATHOLOGY, 2003, 16 (02) :173-182
[6]   Predicting the HER2 status of breast cancer from basic histopathology data: an analysis of 1500 breast cancers as part of the HER2000 International Study [J].
Bilous, M ;
Ades, C ;
Armes, J ;
Bishop, J ;
Brown, R ;
Cooke, B ;
Cummings, M ;
Farshid, G ;
Field, A ;
Morey, A ;
McKenzie, P ;
Raymond, W ;
Robbins, P ;
Tan, L .
BREAST, 2003, 12 (02) :92-98
[7]   Enhanced activation of epidermal growth factor receptor caused by tumor-derived E-cadherin mutations [J].
Bremm, Anja ;
Walch, Axel ;
Fuchs, Margit ;
Mages, Joerg ;
Duyster, Justus ;
Keller, Gisela ;
Hermannstaedter, Christine ;
Becker, Karl-Friedrich ;
Rauser, Sandra ;
Langer, Rupert ;
von Weyhern, Claus Hann ;
Hoefler, Heinz ;
Luber, Birgit .
CANCER RESEARCH, 2008, 68 (03) :707-714
[8]   Real Time RT-PCR Approach for the Evaluation of ERBB2 Overexpression in Breast Cancer Archival Samples: A Comparative Study With FISH, SISH, and Immunohistochemistry [J].
Capizzi, Elisa ;
Gruppioni, Elisa ;
Grigioni, Antonia D'Errico ;
Gabusi, Elena ;
Grassigli, Alberto ;
Grigioni, Walter Franco ;
Fiorentino, Michelangelo .
DIAGNOSTIC MOLECULAR PATHOLOGY, 2008, 17 (04) :220-226
[9]   HER-2 status in breast cancer - Correlation of gene amplification by FISH with immunohistochemistry expression using advanced cellular imaging system [J].
Ciampa, Armando ;
Xu, Bo ;
Ayata, Gamze ;
Baiyee, Daniel ;
Wallace, Jan ;
Wertheimer, Michael ;
Edmiston, Kathryn ;
Khan, Ashraf .
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2006, 14 (02) :132-137
[10]   TYROSINE KINASE RECEPTOR WITH EXTENSIVE HOMOLOGY TO EGF RECEPTOR SHARES CHROMOSOMAL LOCATION WITH NEU ONCOGENE [J].
COUSSENS, L ;
YANGFENG, TL ;
LIAO, YC ;
CHEN, E ;
GRAY, A ;
MCGRATH, J ;
SEEBURG, PH ;
LIBERMANN, TA ;
SCHLESSINGER, J ;
FRANCKE, U ;
LEVINSON, A ;
ULLRICH, A .
SCIENCE, 1985, 230 (4730) :1132-1139