Chromosome 7 Aneusomy in Metaplastic Breast Carcinomas With Chondroid, Squamous, and Spindle-Cell Differentiation

被引:5
作者
Gwin, Katja [1 ,2 ]
Lezon-Geyda, Kimberly [3 ]
Harris, Lyndsay [3 ]
Tavassoli, Fattaneh A. [2 ]
机构
[1] Univ Chicago, Med Ctr, Dept Pathol, Chicago, IL 60637 USA
[2] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[3] Yale Univ, Yale Comprehens Canc Ctr, New Haven, CT 06520 USA
关键词
breast; carcinoma; metaplastic; basal-like tumors; EGFR; gene copy number; GROWTH-FACTOR RECEPTOR; GENE COPY NUMBER; IN-SITU HYBRIDIZATION; ACTIVATING MUTATIONS; PROTEIN EXPRESSION; LUNG-CANCER; HEPATOCELLULAR-CARCINOMA; MALIGNANT MELANOMAS; PLOIDY ANALYSIS; POOR-PROGNOSIS;
D O I
10.1177/1066896909334127
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Metaplastic breast carcinomas (MBCs) are basal-like tumors that frequently express epidermal growth factor receptor (EGFR) via an unknown underlying genetic mechanism. In this study, the EGFR/CEP7 gene copy number in 17 MBCs with chondroid, squamous, and spindle-cell differentiation showing EGFR expression by immunohistochemistry was analyzed using fluorescence in situ hybridization. All cases had a balanced EGFR/CEP7 ratio. EGFR gene amplification was not observed in any case. Monosomy was found in 25% and polysomy in 12.5% of carcinomas with chondroid differentiation. All spindle-cell carcinomas and 50% of squamous carcinomas showed trisomy. Comparison with CEP7 copy number revealed aneusomy of chromosome 7, as opposed to increases or decreases specific to the EGFR gene or 7p. Although no direct correlation between EGFR expression by immunohistochemistry and aneusomy was observed, cases with a score of 3+ showed a higher frequency of EGFR gene copy gain. In the absence of EGFR amplification, chromosome 7 aneusomy might be a useful criterion for the determination of potential candidates for EGFR tyrosine kinase inhibitor clinical trials.
引用
收藏
页码:20 / 25
页数:6
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