Egfr Amplification Specific Gene Expression in Phyllodes Tumours of the Breast

Bibliographic Details
Title: Egfr Amplification Specific Gene Expression in Phyllodes Tumours of the Breast
Authors: Konstantin Agelopoulos, Christian Kersting, Eberhard Korsching, Hartmut Schmidt, Arno Kuijper, Christian August, Pia Wülfing, Joke Tio, Werner Boecker, Paul J. van Diest, Burkhard Brandt, Horst Buerger
Source: Cellular Oncology, Vol 29, Iss 6, Pp 443-451 (2007)
Publisher Information: Wiley, 2007.
Publication Year: 2007
Collection: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
LCC:Cytology
Subject Terms: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Cytology, QH573-671
More Details: Background: Recently, we were able to show that amplifications of the epidermal growth factor receptor (egfr) gene and the overexpression of EGFR were associated with the initiation and progression of phyllodes tumours. Methods: In order to gain further insights into regulation mechanisms associated with egfr amplifications and EGFR expression in phyllodes tumours, we performed global gene expression analysis (Affymetrix A133.2) on a series of 10 phyllodes tumours, of these three with and seven without amplifications of an important regulatory repeat in intron 1 of egfr (CA-SSR I). The results were verified and extended by means of immunohistochemistry using the tissue microarray method on an extensively characterized series of 58 phyllodes tumours with antibodies against caveolin-1, eps15, EGF, TGF-α, pErk, pAkt and mdm2. Results: We were able to show that the presence of egfr CA-SSR I amplifications in phyllodes tumours was associated with 230 differentially expressed genes. Caveolin-1 and eps15, involved in EGFR turnover and signalling, were regulated differentially on the RNA and protein level proportionally to egfr gene dosage. Further immunohistochemical analysis revealed that the expression of caveolin-1 and eps15 were also significantly correlated with the expression of pAkt (p < 0.05), pERK (p < 0.05), mdm2 (p < 0.01) and EGF (p < 0.001 for caveolin-1). Eps15 and pERK were further associated with tumour grade (p < 0.01 and p < 0.001, respectively). Conclusion: Our results show that amplifications within regulatory sequences of egfr are associated with the expression of eps15 and caveolin-1, indicating an increased turnover of EGFR. The interplay between EGFR and caveolin-1, eps15, pAkt, mdm2 and pERK therefore seems to present a major molecular pathway in carcinogenesis and progression of breast phyllodes tumours.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1570-5870
1875-8606
Relation: https://doaj.org/toc/1570-5870; https://doaj.org/toc/1875-8606
DOI: 10.1155/2007/754712
Access URL: https://doaj.org/article/5d684dfded754d7a9efee4a8867143ad
Accession Number: edsdoj.5d684dfded754d7a9efee4a8867143ad
Database: Directory of Open Access Journals
More Details
ISSN:15705870
18758606
DOI:10.1155/2007/754712
Published in:Cellular Oncology
Language:English