Abstract | BACKGROUND: The aim of this study was to determine ERBB-2 (HER-2/neu) gene alterations in different subtypes of uterine sarcomas. METHODS: After central review, representative biopsies were immunohistochemically stained and semiquantitatively scored as negative, weakly (1+), moderately (2+), or strongly (3+) positive. Subsequently, fluorescence in situ hybridization (FISH) was performed on cases with 2+ and 3+ expression. RESULTS: Seventy tumors (52 primaries and 18 recurrent) were evaluated. All 10 adenosarcomas, 21 endometrial stromal sarcomas, and 10 leiomyosarcomas were negative both in the primary and recurrent setting. Twenty-two primary carcinosarcomas were scored. The epithelial component was negative/1+ in 16 (73%), 2+/3+ in five (22.5%) tumors, and could not be evaluated in one case (4.5%), whereas the sarcoma component stained negative/1+ in 21 cases (95.5%) and 3+ (4.5%) in one case. In two recurrent carcinosarcomas, the epithelial component stained 3+ in both cases, whereas the sarcoma component scored negative and 1+. Amplification of the ERBB-2 gene as determined by FISH was observed in 3/7 (43%) carcinosarcomas with 2+ or 3+ overexpression, resulting in an overall 3/22 (14%) amplification rate. One out of four undifferentiated uterine sarcomas stained 2+. ERBB-2 immunopositivity (3+) and ERBB-2 amplification by FISH were confirmed in the recurrent tumor, resulting in a gene amplification rate of 1/4 in undifferentiated uterine sarcomas. CONCLUSION:
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Authors | Frederic Amant, Veerle Vloeberghs, Heidi Woestenborghs, Maria Debiec-Rychter, Lieve Verbist, Philippe Moerman, Ignace Vergote |
Journal | Gynecologic oncology
(Gynecol Oncol)
Vol. 95
Issue 3
Pg. 583-7
(Dec 2004)
ISSN: 0090-8258 [Print] United States |
PMID | 15581967
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Adenosarcoma
(genetics, metabolism)
- Carcinosarcoma
(genetics, metabolism)
- Female
- Gene Amplification
- Genes, erbB-2
(genetics)
- Humans
- Immunohistochemistry
- In Situ Hybridization, Fluorescence
- Interphase
(genetics)
- Leiomyosarcoma
(genetics, metabolism)
- Receptor, ErbB-2
(biosynthesis, genetics)
- Sarcoma
(genetics, metabolism)
- Sarcoma, Endometrial Stromal
(genetics, metabolism)
- Uterine Neoplasms
(genetics, metabolism)
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