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EGFR protein overexpression correlates with chromosome 7 polysomy and poor prognostic parameters in clear cell renal cell carcinoma

Authors :
Đorđević Gordana
Matušan Ilijaš Koviljka
Hadžisejdić Ita
Maričić Anton
Grahovac Blaženka
Jonjić Nives
Source :
Journal of Biomedical Science, Vol 19, Iss 1, p 40 (2012)
Publication Year :
2012
Publisher :
BMC, 2012.

Abstract

Abstract Background The role of epidermal growth factor (EGF) and its receptor (EGFR) in the pathogenesis and progression of various malignant tumors has long been known, but there is still disagreement concerning prognostic significance of EGFR expression in clear cell renal cell carcinoma (CCRCC). The present study was designed to analyze more objectively the protein EGFR expression in CCRCC and to compare its value with EGFR gene copy number changes and clinicopathologic characteristics including patient survival. Methods The protein EGFR expression was analyzed immunohistochemically on 94 CCRCC, and gene copy number alterations of EGFR by FISH analysis on 41 CCRCC selected according to distinct membrane EGFR staining. Results Membrane EGFR expression in tumor cells was heterogeneous with respect to the proportion of positive cells and staining intensity. FISH analysis did not reveal EGFR gene amplification, while polysomy of chromosome 7 found in 41% was associated with higher EGFR membrane expression. Moreover, EGFR overexpression was associated with a higher nuclear grade, larger tumor size and shorter patient's survival, while there was no connection with pathological stage. Conclusion In conclusion, the protein expression of EGFR had an impact on prognosis in patients with CCRCC, while an increased copy number of chromosome 7 could be the possible reason for EGFR protein overexpression in the absence of gene amplification.

Details

Language :
English
ISSN :
14230127 and 10217770
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Biomedical Science
Publication Type :
Academic Journal
Accession number :
edsdoj.bba75f821d2d455498756c902f36db53
Document Type :
article
Full Text :
https://doi.org/10.1186/1423-0127-19-40