Analysis of the immunoreactivity of three anti-p53 antibodies and estimation of the relations between p53 status and MDM2 protein expression in ovarian carcinomas

Citation
A. Harlozinska et al., Analysis of the immunoreactivity of three anti-p53 antibodies and estimation of the relations between p53 status and MDM2 protein expression in ovarian carcinomas, ANTICANC R, 20(2A), 2000, pp. 1049-1056
Citations number
40
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
2A
Year of publication
2000
Pages
1049 - 1056
Database
ISI
SICI code
0250-7005(200003/04)20:2A<1049:AOTIOT>2.0.ZU;2-1
Abstract
Background. The p53 growth suppressor is inactivated in human tumors by sev eral distinct mechanisms, such as point mutations, binding to viral protein s and association with the MDM2 protein. Little is known about the expressi on of different immunologically distinct forms of p53 and MDM2 protein in h uman tumors and especially in ovarian carcinomas. Materials and Methods. Th e overexpression of p53 and MDM2 onco-proteins was examined in a series of 46 ovarian carcinomas, taking into account the conventional pathological va riables. The comparison of p53 and MDM2 expression in tissue sections and r espective cyst and-or ascitic fluid cells was also performed. For the deter mination of the p53 expression the reactivity of three commonly used anti-p 53 antibodies (DO7, PAb240, PAb1620), which detect immunologically distinct subclasses of p53, were analyzed in relation to the MDM2 status in individ ual patients. Results. The detection of the p53 expression was clearly rela ted to the antibody applied. DO7 antibody appears to be superior to both PA b240 and PAb1620 in immunohistochemical tests. Nuclear MDM2 protein overexp ression was found in 17.4% of cases and usually it was associated with p53 accumulation There was no significant correlation between p53 as well as MD M2 expression and histological subtypes, staging and grading parameters of carcinomas however p53 accumulation was detected more often in III/IV than in I/II FIGO stages. Conclusion. In ovarian carcinomas significant inter- a nd intra-tumoral heterogeneity in p53 and MDM2 expression was identified an d different MDM2/p53 phenotypes were revealed. The restriction of MDM2 over expression to a small subset of neoplasms indicates that this oncoprotein p lays a minor role in ovarian carcinogenesis.