S. Marsigliante et al., EFFECT OF TUMOR SIZE ON THE ASSOCIATION BETWEEN PS2 AND CATHEPSIN-D IN PRIMARY BREAST-CANCER, International journal of oncology, 6(1), 1995, pp. 69-73
Previous studies have shown that pS2 and cathepsin D are linked in lym
ph node positive (N+) tumours, but not in tumours from lymph node nega
tive (N-) patients. The purpose of this study was to understand whethe
r or not size would effect the relationship between pS2 and cathepsin
D. Findings were further extended to some subgroups of tumours obtaine
d stratifying for T and N and particularly to the small (TI) but aggre
ssive (N+) cancers (T1/N+) and to those of size greater than 2 cm (T2
and T3) but yet node negative (T2+T3/N-). Oestrogen (ER) and progester
one (PR) receptors, pS2 and cathepsin D concentrations were therefore
assayed in 355 primary breast cancers. ER, PR, pS2 and cathepsin D did
not correlate to nodal status and size of the tumours; no significant
differences in the expression of these four biological factors betwee
n infiltrating ductal carcinomas without special features (NOS) and no
n-NOS carcinomas were found. Multivariate analysis performed among cat
hepsin D, ER, PR and pS2 indicated that, in T1 tumours, pS2 was the mo
st important variable and the best predictor in cathepsin D determinat
ion, while such association was absent in T2 and T3 tumours. pS2 and c
athepsin D significantly associated also in tumours obtained from N+ p
atients, and such correlation was highest in T1 tumours with positive
axillary nodes (N+/T1). pS2 and cathepsin D did not associate in tumou
rs taken from N- patients. Considering the NOS carcinomas, correlation
between pS2 and cathepsin D in the N+, T1 and N+/T1 subgroups was hig
her in the poorly differentiated grade 3 with respect to grade 1 and g
rade 2 cancers. The data suggest that pS2 could have a role in catheps
in D expression and we hypothesise that such control could be an early
biological event occurring in the development and progression of part
icularly aggressive (N+/grade 3), small (T1) breast cancers.