Whether or not breast cancer screening results in a reduction in mortality from the disease, it is clear from several studies that screening yields tumours that are smaller, more likely to be in situ and clinically less advanced (Linell et al., 1980;Gibbs, 1985;Anderson et al., 1986;Roberts et al., 1990 al., 1982], Amersham) diluted 1/40 in 1/5 normal swine serum. The sections were then incubated for 30min with biotinylated sheep-anti-mouse serum (Amersham) and streptavidinbiotin peroxidase complex for 30min, being washed with TBS between stages. The chromagen and counterstain were as for the c-erbB-2 method above. A section of human placenta was used as a control.Tumours were scored on a basis of intensity and distribution of staining as previously described (Horne, 1987). Both membrane and cytoplasmic staining was considered. Carcinomas showing definite labelling of greater than 25% of tumour cells were regarded as 'positive'. Cathepsin D Paraffin sections were cut at 4 ts, dewaxed, rehydrated and treated with hydrogen peroxide in methanol as for c-erbB-2 above. They were next treated with 0.1% trypsin at 37°C for 10 min and washed in water. After rinsing in TBS and incubation with normal 1/5 swine serum for 10 min as above, they were incubated with the primary antiserum (anti-cathepsin D [Reid et al., 1986]) diluted 1:400 for 30 min at RT. After two changes of TBS they were incubated with biotinylated donkey-anti-rabbit serum (Amersham) and streptavidin-biotin peroxidase complex for 30 min, being washed with TBS between stages. The chromagen and counterstain were as for the c-erbB-2 method above.Tumours were scored for intensity of staining as previously described ) and placed in three grades, 0, no cell staining; 1, moderate staining; 2, strong staining.