H. Moch et al., EGF-R GENE COPY NUMBER CHANGES IN RENAL-CELL CARCINOMA DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION, Journal of pathology, 184(4), 1998, pp. 424-429
Expression of epidermal growth factor receptor (EGF-r) is a frequent e
vent in renal cell carcinoma (RCC). To investigate the role of EGF-r g
ene copy number changes related to EGF-r overexpression, 50 RCC specim
ens were examined by fluorescence in situ hybridization (FISH) and imm
unohistochemistry. Dual-labelling FISH with a repetitive pericentromer
ic probe for chromosome 7 and a probe for the ECF-r gene (at 7p13) was
performed to analyse the EGF-r copy number in relation to chromosome
7 copy number on a cell-by-cell basis. Polysony 7 was frequent in all
histological types of RCC. Chromosome 7 polysomy was found in 26 of 35
clear cell (74 per cent), nine of nine papillary, and three of three
chromophobe RCCs. EGF-r gene copy number was closely associated with t
he chromosome 7 copy number on a cell-by-cell basis. No EGF-r gene amp
lifications were found. EGF-r positivity was found in 37 of 50 cases (
74 per cent) by immunohistochemistry. EGF-r positivity was more common
in clear cell (81 per cent) than in papillary tumours (40 per cent; P
=0.029). Neither chromosome 7 nor ECF-r gene copy number was associate
d with ECF-r expression, indicating that an increased gene dosage is n
ot a mechanism of EGF-r overexpression in RCC. (C) 1998 John Wiley & S
ons, Ltd.