Nuclear survivin expression is a positive prognostic factor in taxane-platinum-treated ovarian cancer patients
Authors:
- Anna Felisiak-GolabekAFAnna Felisiak-Golabek
- Alina RembiszewskaARAlina Rembiszewska
- Iwona K RzepeckaIRIwona K Rzepecka
- Lukasz SzafronLSLukasz Szafron
- Radoslaw MadryRMRadoslaw Madry
- Magdalena MurawskaMagdalena Murawska
- Tomasz NapiorkowskiTNTomasz Napiorkowski
- Piotr SobiczewskiPSPiotr Sobiczewski
- Beata OsuchBOBeata Osuch
- Jolanta KupryjanczykJKJolanta Kupryjanczyk
- the Polish Ovarian Cancer Study Group (POCSG)T(the Polish Ovarian Cancer Study Group (POCSG)
Open Access
- 10 November 2011
- journal article
- Published by Springer Nature in Journal of Ovarian Research
- Vol. 4 (1) , 20
Abstract
Background: Survivin is an inhibitor of apoptosis and a regulator of mitotic progression. TP53 protein is a negative transcriptional regulator of survivin. The aim of our study was to evaluate the clinical significance of survivin expression in advanced stages ovarian cancer with respect to the TP53 status.Methods: Survivin and TP53 expression was evaluated immunohistochemically in 435 archival samples of ovarian carcinomas (244 patients were treated with platinum/cyclophosphamide-PC/PAC; 191-with taxane-platinum (TP) agents). Univariate and multivariate statistical analyses were performed in patients groups divided according to the administered chemotherapeutic regimen, and in subgroups with and without TP53 accumulation (TP53+ and TP53-, respectively).Results: Nuclear and cytoplasmic survivin expression was observed in 92% and 74% of the carcinomas, respectively. In patients treated with TP, high nuclear survivin expression decreased the risk of disease recurrence and death, and increased the probability of high platinum sensitivity (p < 0.01), but only in the TP53(+) group, and not in the TP53(-) group.Conclusions: It appears that TP53 status determines the clinical importance of nuclear survivin expression in taxane-platinum treated ovarian cancer patients.Keywords
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