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pubmed-article:12441262pubmed:abstractTextOverexpression of the epidermal growth factor receptor (EGFR) often correlates with an aggressive tumour phenotype and poor prognosis. To examine the relevance of EGFR in colorectal cancer, we determined the expression of EGFR protein in 249 colorectal adenocarcinomas and 42 lymph node metastases using immunohistochemistry. Moreover, we investigated a (CA)(n) dinucleotide repeat polymorphism of the EGFR gene in a subset of 114 tumours. High levels of EGFR protein were observed in 123/249 (49.4%) samples. EGFR expression in colorectal carcinomas correlated with differentiation grade (P=0.014). However, there were no associations with Dukes' stage, site, patient age or gender. EGFR protein expression did not influence survival in this colorectal cancer patient cohort (P>or=0.05). Expression was not identical in paired colorectal tumours and lymph node metastases, with only 17/42 (40.5%) samples showing equivalent EGFR levels (P>0.05). The distribution of the (CA)(n) dinucleotide repeat alleles in colorectal adenocarcinomas was not associated with EGFR protein expression (P>0.05). These results indicate that while EGFR overexpression is a common event in colorectal carcinogenesis, it does not influence patient prognosis.lld:pubmed
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pubmed-article:12441262pubmed:authorpubmed-author:CassidyJJlld:pubmed
pubmed-article:12441262pubmed:authorpubmed-author:ClarkCClld:pubmed
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pubmed-article:12441262pubmed:authorpubmed-author:MurrayG IGIlld:pubmed
pubmed-article:12441262pubmed:authorpubmed-author:MurrayL JLJlld:pubmed
pubmed-article:12441262pubmed:authorpubmed-author:McKayJ AJAlld:pubmed
pubmed-article:12441262pubmed:authorpubmed-author:RossV GVGlld:pubmed
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pubmed-article:12441262pubmed:pagination2258-64lld:pubmed
pubmed-article:12441262pubmed:dateRevised2009-11-19lld:pubmed
pubmed-article:12441262pubmed:articleTitleEvaluation of the epidermal growth factor receptor (EGFR) in colorectal tumours and lymph node metastases.lld:pubmed
pubmed-article:12441262pubmed:affiliationDepartment of Medicine and Therapeutics, University of Aberdeen, Foresterhill, AB25 2ZD, Aberdeen, UK.lld:pubmed
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