Epidermal Growth Factor Receptor Expression and Gene Copy Number in the Risk of Oral Cancer

Mohammed Taoudi Benchekroun(University of Maryland, Baltimore), Pierre Saintigny(University of Maryland, Baltimore), Sufi M. Thomas(University of Maryland, Baltimore), Adel K. El‐Naggar(University of Maryland, Baltimore), Vassiliki A. Papadimitrakopoulou(University of Maryland, Baltimore), Hening Ren(University of Maryland, Baltimore), Wenhua Lang(University of Maryland, Baltimore), You-Hong Fan(University of Maryland, Baltimore), Jianhua Huang(University of Maryland, Baltimore), Lei Feng(University of Maryland, Baltimore), J. Jack Lee(University of Maryland, Baltimore), Edward S. Kim(University of Maryland, Baltimore), Waun Ki Hong(University of Maryland, Baltimore), Faye M. Johnson(University of Maryland, Baltimore), Jennifer R. Grandis(University of Maryland, Baltimore), Li Mao(University of Maryland, Baltimore)
Cancer Prevention Research
June 23, 2010
Cited by 131Open Access
Full Text

Abstract

UNLABELLED: Leukoplakia is the most common premalignant lesion of the oral cavity. Epidermal growth factor receptor (EGFR) abnormalities are associated with oral tumorigenesis and progression. We hypothesized that EGFR expression and gene copy number changes are predictors of the risk of an oral premalignant lesion (OPL) progressing to oral squamous cell carcinoma (OSCC). A formalin-fixed, paraffin-embedded OPL biopsy specimen was collected from each of 162 patients in a randomized controlled clinical trial. We assessed EGFR expression by immunohistochemistry with two METHODS: a semiquantitative analysis (145 evaluable specimens) and an automated quantitative analysis (127 evaluable specimens). EGFR gene copy number was assessed by fluorescence in situ hybridization (FISH) in a subset of 49 OPLs with high EGFR expression defined by the semiquantitative analysis. We analyzed EGFR abnormalities for associations with OSCC development. High EGFR expression occurred in 103 (71%) of the 145 OPLs and was associated with a nonsignificantly higher risk of OSCC (P = 0.10). Twenty (41%) of 49 OPLs assessed by FISH had an increased EGFR gene copy number (FISH-positive). Patients with FISH-positive lesions had a significantly higher incidence of OSCC than did patients with FISH-negative (a normal copy number) lesions (P = 0.0007). Of note, 10 of 11 OSCCs that developed at the site of the examined OPL were in the FISH-positive group, leaving only one FISH-negative OPL that did so (P < 0.0001). Our data indicate that an increased EGFR gene copy number is common in and associated with OSCC development in patients with OPLs expressing high EGFR, particularly OSCC developing at the site of a high-expression OPL; they also suggest that EGFR inhibitors may prevent oral cancer in patients with OPLs having an increased EGFR gene copy number.


Related Papers

No related papers found

Powered by citation graph analysis