In this study the expression of c-erbB-3 protein was investigated in a
range of human ovarian tumours using a monoclonal antibody (RTJ1) rai
sed to a synthetic peptide from the cytoplasmic domain of the human c-
erbB-3 protein. A total of 73 samples from 71 patients were graded as
negative, weak, moderate or strong according to the intensity of immun
ohistochemical staining observed, and this was related to tumour chara
cteristics and other clinical parameters. In terms of positivity vs ne
gativity, of the 73 samples examined, 62 (85%) showed positive immunoh
istochemical staining for c-erbB-3. The majority of all ovarian tumour
s studied were positive for c-erbB-3 regardless of whether they were m
alignant (89%), borderline (100%) or benign (61%), however the inciden
ce of positivity was significantly less in the benign group than in ov
ertly malignant tumours (P = 0.03). c-erbB-3 positivity was not signif
icantly associated with either age at diagnosis, tumour stage, differe
ntiation, ploidy, percentage in 5-phase or post-operative tumour bulk
in malignant tumours. In terms of intensity of staining no significant
difference was observed either within the common epithelial group or
between this group and tumours of a benign nature. A significantly mor
e intense pattern of c-eubB-3 staining was observed in tumours of bord
erline malignancy when compared with their overtly malignant counterpa
rts (P = 0.002). Patients presenting with early-stage malignant tumour
s (I/II) were more likely to display intense tumour staining than thos
e with late-stage disease (III/IV) (P = 0.04). These investigations su
ggest that c-erbB-3 protein is frequently expressed in both benign and
malignant ovarian tumours, and that overexpression is more common in
borderline and early invasive lesions.