M. Bellotti et al., MORPHOMETRIC DETERMINATION OF AGNORS IN BREAST-CARCINOMA - CORRELATION WITH FLOW-CYTOMETRY AND PROLIFERATING CELL NUCLEAR ANTIGEN, Analytical and quantitative cytology and histology, 19(2), 1997, pp. 139-144
To determine the relationship beween argyrophilic nucleolar organizer
regions (AgNORs), ploidy and proliferative activity in breast carcinom
as. STUDY DESIGN: AgNOR staining was performed in 25 cases of infiltra
ting ductal carcinoma of the breast, and several features were quantif
ied by image analysis: nuclear area, mean value of the number of AgNOR
s (M_N_Ag), area of AgNORs (A_Ag), area of AgNOR per nucleus (A_Ag/N),
A_Ag variance (A_Ag_V) and coefficient of variation of AgNOR area per
nucleus (CV_A_Ag/N). These findings were correlated with ploidy and p
roliferative activity obtained by flow cytometry, also quantifying the
latter with proliferating cell nuclear antigen (PCNA). Comparison of
AgNORs with size of the tumor and lymph Mode status was also made. RES
ULTS: We observed a good correlation between M_N_Ag and A_Ag with ploi
dy (P<.001), M_N_Ag and A_Ag with S-phase fraction (SPF) (P <.001), A_
Ag with S+G2M (P<.02) and PCNA with M_N_Ag (P <.05). The mean value of
A_Ag allowed division of the cases into two groups: diploid (D) and n
ear diploid (ND) with low SPF (A_Ag < = 2.50 mu m(2)), and D and ND wi
th high SPF and aneuploidy (A) (A_Ag > 2.50 mu m(2)) (P<.05). There wa
s a statistically significant correlation between M_N_Ag and A_Ag and
between tumor size and lymph node metastases (P<.05).CONCLUSION: AgNOR
s correlate with various cell cycle and clinicopathologic features and
will be used eventually as prognostic markers in breast cancer.