C. Charpin et al., CD31 QUANTITATIVE IMMUNOCYTOCHEMICAL ASSAYS IN BREAST CARCINOMAS - CORRELATION WITH CURRENT PROGNOSTIC FACTORS, American journal of clinical pathology, 103(4), 1995, pp. 443-448
The distribution of PECAM-1/CD31 molecule was investigated in 133 brea
st carcinomas using monoclonal antibody and frozen sections. Anti-CD31
labels endothelial cells and reflects stromal angiogenesis. The CD31
immunoreactivity was evaluated by computer-assisted analysis of digiti
zed microscopic images. The automatic screening of the whole preparati
on and the measurements of the mean CD31 immunostained surface was per
formed in each case. A similar procedure was achieved for p53, catheps
in D, P-gp, pHer-2/neu, Ki67, pS2 estrogen and progesterone antigenic
sites immunodetection. The image analysis of positive CD31 surface was
variable, ranging from 4% to 33% (mean 14.7%, SD = 5.43). The CD31 po
sitive surface correlated (P < .01) with the Nottingham prognostic ind
ex, but not with the tumor size, the node status, the tumor grade, nor
with the patient age. Also the CD31 immunoreactivity was independent
of the pHER-2/neu, Ki67 antigen, p53, ER, PR and pS2 immunodetectable
expression in tumors, but correlates with that of cathepsin D (P = .02
4) and P-gp (P = .028), which reflects the multi-drug resistance capac
ity of tumor cells. In conclusion, CD31 positive vessels assessed on f
rozen sections by image analysis constitute an excellent method of eva
luating tumor stromal angiogenesis, and can be further used for clinic
al purposes. The results also suggest that the CD31/PECAM molecule may
be involved in the spread of tumor by interacting with extracellular
matrix lysis that results from the tumor cell proteasic activity and w
ith multidrug resistance.