Evaluation of Her-2/neu Status in Carcinomas With Amplified Chromosome 17 Centromere Locus
Author(s) -
Megan L. Troxell,
Charles D. Bangs,
Helen J. Lawce,
Ilana Galperin,
Daniel Baiyee,
Robert B. West,
Susan B. Olson,
Athena M. Cherry
Publication year - 2006
Publication title -
american journal of clinical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.859
H-Index - 128
eISSN - 1943-7722
pISSN - 0002-9173
DOI - 10.1309/9eym6ve58f2ycd9f
Subject(s) - fluorescence in situ hybridization , centromere , biology , chromosome 17 (human) , immunohistochemistry , polysomy , locus (genetics) , amplicon , chromosome , microbiology and biotechnology , marker chromosome , breast carcinoma , pathology , genetics , breast cancer , karyotype , gene , cancer , medicine , immunology , polymerase chain reaction
Accurate assessment of Her-2/neu (erb-b2) status in breast carcinoma is essential for therapy planning. Clinical assays are targeted at protein overexpression (immunohistochemical analysis) or gene amplification (fluorescence in situ hybridization [FISH]). Cases with aberrant FISH signal patterns are problematic and may lead to underreporting of Her-2/neu amplification. We performed FISH with additional chromosome 17 probes, SMS (Smith-Magenis syndrome critical region) and RARA (retinoic acid receptor), on 7 cases with unusual Her-2/CEP17 (chromosome 17 centromere control probe) results to assess whether different measurements of chromosome 17 copy number might clarify the Her-2/neu amplicon status. Although the Her-2/CEP17 ratio scores were within normal range (<2.0), the Her-2/SMS or Her-2/RARA ratio revealed amplification of Her-2/neu in 5 of 7 cases. Immunohistochemical analysis demonstrated Her-2/neu protein overexpression in the same 5 cases only. We describe novel application of SMS/RARA FISH probes for assessing cases with complex Her-2/CEP17 FISH patterns. Such additional data, correlated with immunohistochemical analysis, may help guide therapy in patients with breast carcinoma.
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