C. Ceccarelli et al., Immunohistochemical expression of internal and external ErbB-2 domains in invasive breast cancer, BREAST CANC, 58(2), 1999, pp. 107-114
We tested three ErbB-2 monoclonal antibodies (MoAbs) specific to the intrac
ytoplasmic internal domain (clone CB 11) and the extracellular glycosylated
peptide domain (clones CBE1 and Tab250) in 351 primary invasive breast car
cinomas. ErbB-2 immunodetection allowed us to differentiate three main grou
ps: group 1 (62.7%) lacked both MoAb ErbB-2 domains (erb -/-); group 2 stai
ned for both domains (erb +/+) (26.5%); group 3 stained for the internal do
main only (erb +/-) (10.8%). The relationships among these groups and nodal
status (N) were statistically significant, with N+ cases reaching the high
est value (89.2%) in the erb +/- group. Lack of immunostaining in the exter
nal domain thus seems to be associated with increased metastatic spread. At
variance analysis the difference in hormonal receptor content between grou
ps 1 and 3 was not significant; while between groups 1 and 2 it was. The gr
owth fraction of groups 2 and 3 was significantly higher than that of group
1. Our results showed that anti-ErbB-2 MoAb clone CB 11 was able to detect
a higher number of ErbB-2 expressing cases than the two that are specific
for the external domain (clones Tab 250 and CBE1). Due to the strong associ
ation between group 3 cases and the highest metastatic potential, this aggr
essive group could be identified only with the use of an internal-domain sp
ecific MoAb CB11, which thus seems to present a better discriminative power
as a diagnostic marker in the biopathological characterization of breast c
arcinoma.