Intratumoral heterogeneity of HER-2/neu in invasive mammary carcinomas using fluorescence in-situ hybridization and tissue microarray

被引:40
作者
Shin, Sandra J. [1 ]
Hyjek, Elizabeth [1 ]
Early, Erin [1 ]
Knowles, Daniel M. [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Pathol & Lab Med, New York, NY 10021 USA
关键词
HER-2/neu; gene amplification; intratumoral heterogeneity;
D O I
10.1177/1066896906293055
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Fluorescence in-situ hybridization is increasingly being used to determine HER-2/neu status in patients with breast carcinoma. The possibility that intratumoral heterogeneity of HER-2/neu gene amplification may potentially contribute to inaccurate assessment of HER-2/neu status was investigated in routine cases of invasive mammary carcinomas. From 169 representative formalin-fixed, paraffin-embedded blocks of invasive duct mammary carcinomas with grade 3 architecture, 48 cases were analyzed by fluorescence in-situ hybridization and 59 analyses were performed. Intratumoral heterogeneity for HEB-2/neu gene amplification was demonstrated in only 5 (16%) of 31 cases where morphologically similar areas of a single tumor were analyzed. We conclude from this study that intratumoral heterogeneity of HER-2/neu gene amplification is a demonstrable but relatively uncommon occurrence. For invasive mammary carcinomas, the accurate assessment of HER-2/neu status by fluorescence in-situ hybridization analysis is not significantly confounded by intratumoral heterogeneity of HER-2/neu gene amplification in individual tumors.
引用
收藏
页码:279 / 284
页数:6
相关论文
共 39 条
[1]  
Andersson J, 2004, APPL IMMUNOHISTO M M, V12, P14
[2]   Intratumoral heterogeneity in breast carcinoma revealed by laser-microdissection and comparative genomic hybridization [J].
Aubele, M ;
Mattis, A ;
Zitzelsberger, H ;
Walch, A ;
Kremer, M ;
Hutzler, P ;
Höfler, H ;
Werner, M .
CANCER GENETICS AND CYTOGENETICS, 1999, 110 (02) :94-102
[3]  
BERGER MS, 1988, CANCER RES, V48, P1238
[4]   c-erbB2 overexpression decreases the benefit of adjuvant tamoxifen in early-stage breast cancer without axillary lymph node metastases [J].
Carlomagno, C ;
Perrone, F ;
Gallo, C ;
DeLaurentiis, M ;
Lauria, R ;
Morabito, A ;
Pettinato, G ;
Panico, L ;
DAntonio, A ;
Bianco, AR ;
DePlacido, S .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (10) :2702-2708
[5]   Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease [J].
Cobleigh, MA ;
Vogel, CL ;
Tripathy, D ;
Robert, NJ ;
Scholl, S ;
Fehrenbacher, L ;
Wolter, JM ;
Paton, V ;
Shak, S ;
Lieberman, G ;
Slamon, DJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2639-2648
[6]   Genetic instability of cancer cells is proportional to their degree of aneuploidy [J].
Duesberg, P ;
Rausch, C ;
Rasnick, D ;
Hehlmann, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (23) :13692-13697
[7]   Determination of HER2 gene amplification by fluorescence in situ hybridization and concordance with the clinical trials immunohistochemical assay in women with metastatic breast cancer evaluated for treatment with trastuzumab [J].
Dybdal, N ;
Leiberman, G ;
Anderson, S ;
McCune, B ;
Bajamonde, A ;
Cohen, RL ;
Mass, RD ;
Sanders, C ;
Press, MF .
BREAST CANCER RESEARCH AND TREATMENT, 2005, 93 (01) :3-11
[8]  
EDGARTON SE, 2000, BREAST CANC RES TREA, V64, P55
[9]   A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS [J].
FEARON, ER ;
VOGELSTEIN, B .
CELL, 1990, 61 (05) :759-767
[10]  
Fitzgibbons PL, 2000, ARCH PATHOL LAB MED, V124, P966