Cell cycle-related phosphatases CDC25A and B expression correlates with survival in ovarian cancer patients

Citation
M. Broggini et al., Cell cycle-related phosphatases CDC25A and B expression correlates with survival in ovarian cancer patients, ANTICANC R, 20(6C), 2000, pp. 4835-4840
Citations number
29
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
ISSN journal
02507005 → ACNP
Volume
20
Issue
6C
Year of publication
2000
Pages
4835 - 4840
Database
ISI
SICI code
0250-7005(200011/12)20:6C<4835:CCPCAB>2.0.ZU;2-Z
Abstract
Alterations in cell cycle regulating proteins are common in many cancer typ es. Recent data suggest a possible link between CDC25 phosphatases overexpr ession and malignancy. Our objective was to evaluate the expression of the three cell cycle-related phosphatases CDC25A, CDC25B and CDC25C in patients with ovarian cancer. All the patients had a minimal follow up of three yea rs. CDC25A, CDC25B and CDC25C expression were investigated by immunohistoch emistry in 106 patients with ovarian cancer. CDC25A and CDC25B were found e xpressed in almost all the samples analyzed, while CDC25C was undetectable in more than 80% of the patients. The low evaluable data on CDC25C expressi on, did not allow any association between the expression of this phosphatas e and prognosis. The expression of CDC25A and CDC25B showed some evidences of association with a poor prognosis (p = 0.034 and p = 0.058 respectively) . This relationship was independent of other factors such as tumor grade, h istotype, stage and residual tumor after surgery. In the same patients the examined parameters (residual tumor; grade, stage and histotype) did show t he expected relation with survival. The results indicate that high CDC25A a nd CDC25B expression is related to at worse prognosis in ovarian cancer pat ients. CDC25 phosphatases expression can be regarded as a possible prognost ic factor for ovarian cancer and these proteins should be evaluated as pote ntial molecular targets of novel drugs against this human neoplasm.