IMMUNOHISTOCHEMICAL EXPRESSION OF PS2 AND CATHEPSIN-D IN BREAST-CANCER - RELATIONSHIP WITH ER, PGR IMMUNOSTAININGS AND CLINICOPATHOLOGICAL ASPECTS

Citation
Am. Valentini et al., IMMUNOHISTOCHEMICAL EXPRESSION OF PS2 AND CATHEPSIN-D IN BREAST-CANCER - RELATIONSHIP WITH ER, PGR IMMUNOSTAININGS AND CLINICOPATHOLOGICAL ASPECTS, Oncology Reports, 1(3), 1994, pp. 585-590
Citations number
56
Categorie Soggetti
Oncology
Journal title
ISSN journal
1021335X
Volume
1
Issue
3
Year of publication
1994
Pages
585 - 590
Database
ISI
SICI code
1021-335X(1994)1:3<585:IEOPAC>2.0.ZU;2-P
Abstract
Fifty patients with breast cancer were studied to examine the relation ship between the immunohistochemical tumour expression of pS2 and 52 k ilodalton-cathepsin D (52K-CD) proteins and several biological and cli nical parameters. Our aim was to verify whether these two proteins may provide additional information for the management of breast cancer pa tients. By using a cut-off point of 10% for pS2 and 15% for 52K-CD val uations, we found that 24 of 50 (48%) carcinomas were pS2+ and 26 of 5 0 (52%) were 52K-CD+. A statistically significant positive association was found between pS2 positivity and ER presence (p=0.05), though 36% of ER-patients were pS2+. We did not find any correlation between the 52K-CD expression and other parameters studied, neither pS2. Although our findings confirm previous data correlating significantly the ER p resence with pS2+ cases, we emphasise the necessity to standardize the use of a clinically significant cut-off point in further immunohistoc hemical studies to evaluate this protein and, therefore, to explain it s role also in tumours lacking ER. As regard the 52K-CD, our results a gree with those of other studies, though the association of this enzym e with ER status is controversial in both cytosol and immunohistochemi cal studies, the use of monoclonal antibodies on frozen sections and p olyclonal antibodies on paraffin section can explain this controversy. Our experience indicate the use of an immunohistochemical method in d etection of this enzyme and the use of M1G8 (morioclonal antibody) on paraffin sections to make clear the possible role of 52K-CD in breast cancer.