QUANTITATIVE IMAGE-ANALYSIS OF MIB-1 IMMUNOREACTIVITY - A COMPARISON WITH FLOW CYTOMETRIC ASSESSMENT OF PROLIFERATIVE ACTIVITY IN INVASIVE-CARCINOMA OF THE BREAST
Ml. Ostrowski et al., QUANTITATIVE IMAGE-ANALYSIS OF MIB-1 IMMUNOREACTIVITY - A COMPARISON WITH FLOW CYTOMETRIC ASSESSMENT OF PROLIFERATIVE ACTIVITY IN INVASIVE-CARCINOMA OF THE BREAST, Analytical and quantitative cytology and histology, 17(1), 1995, pp. 15-24
Proliferative activity, especially flow cytometrically determined S-ph
ase fraction, is generally accepted as an important prognostic indicat
or in carcinoma of the breast. We studied cellular proliferation in 53
breast carcinomas using quantitative image analysis of immunoreactivi
ty to a recently available monoclonal antibody, MIB-1, which is applic
able to formalin-fixed, paraffin-embedded tissues. A MIB-1 is a murine
monoclonal antibody that reacts with the Ki-67 nuclear antigen expres
sed by proliferating cells in the late G1, and G2/M phases of the cell
cycle. These results were compared to pow cytometric determinations o
f S-phase and S + G2/M phase fractions obtained from corresponding fre
sh tissue samples. There was a good correlation between quantitative i
mmunoreactivity to MIB-1 as measured by image analysis and pow cytomet
ric S-phase and S + G2/M phase fractions (r=.63, P<.00001; r=.607, P<.
00001, respectively). Immunoreactivity to MIB-1 and flow cytometric S-
phase and S + G2/M phase fractions were significantly increased in ane
uploid tumors as compared to diploid tumors. Histologic grade correlat
ed with flow cytometric S-phase and S + G2/M phase fractions and MlB-1
immunoreactivity as determined by image analysis. There was a correla
tion between tumor size and MIB immunoreactivity. No proliferative par
ameters significantly correlated with lymph node status. Assessment of
proliferative activity by quantitative image analysis of immunoreacti
vity to monoclonal MIB-1 antibody may be employed in cases of invasive
carcinoma of the breast in which flow cytometric analysis fails to re
sult in quantitative proliferative values, or it may be used as an alt
ernative measurement of such proliferative activity.