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Evaluation of c-erbB-2 Expression, Amplification, and Prognostic Value in Primary and Metastatic Prostate Adenocarcinomas
Author(s) -
Arbil Açıkalın,
Şeyda Erdoğan,
Emine Kılıç Bağır,
Volkan İzol,
Zühtü Tansuğ,
Gülşah Şeydaoğlu,
Suzan Zorludemir,
Gülfiliz Gönlüşen
Publication year - 2014
Publication title -
erciyes medical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.101
H-Index - 11
ISSN - 1300-199X
DOI - 10.5152/etd.2014.8157
Subject(s) - prostate , medicine , immunohistochemistry , fluorescence in situ hybridization , metastasis , primary tumor , oncology , prostate cancer , stage (stratigraphy) , prostate carcinoma , gene duplication , pathology , pathological , cancer research , gene , biology , cancer , paleontology , biochemistry , chromosome
Objective: The c-erbB-2 gene codes for a membrane receptor protein that is homologous to the epidermal growth factor recep- tor. It has been established as a prognostic factor in breast and other cancers. The prognostic role of c-erbB-2 expression and gene amplification in prostate carcinoma is still controversial. In this study, we searched for c-erbB-2 overexpression and gene amplification in primary and metastatic prostate carcinomas and their correlation with tumor grade, age, and survival. Material and Methods: c-erbB-2 protein overexpression was analyzed on 59 prostate carcinomas, including 44 primary and 15 metastatic prostate carcinomas, by immunohistochemistry and fluorescence in situ hybridization analysis. Results: When divided into two Gleason grade categories, there were 20 low-grade and 24 high-grade cases in the primary pros- tate carcinoma cases. C-erbB-2 overexpression was detected in 13.6% of primary and in 60% of metastatic prostate carcinomas. The overexpression was correlated with Gleason score (p=0.001) and clinical outcome but not with age (p>0.05). None of the cases showed HER-2 amplification by FISH. Conclusion: In this study, c-erbB-2 protein overexpression was associated with high grade and advanced pathological stage. Ad- ditionally, it was also associated with metastatic prostate tumors. These findings support that this marker indicates a potentially aggressive clinical course and metastasis. Therefore, this marker may be helpful for planning therapy.

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