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Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis

Background: Survivin belongs to the protein family of inhibitors of apoptosis (IAP) and is a regulator of the cell cycle and apoptosis. The aim of this study was to assess the clinical and prognostic significance of expression survivin in patients with ovarian cancer. Methods: We systematically sear...

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Autores principales: Gąsowska-Bajger, Beata, Gąsowska-Bodnar, Agnieszka, Knapp, Paweł, Bodnar, Lubomir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924601/
https://www.ncbi.nlm.nih.gov/pubmed/33669912
http://dx.doi.org/10.3390/jcm10040879
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author Gąsowska-Bajger, Beata
Gąsowska-Bodnar, Agnieszka
Knapp, Paweł
Bodnar, Lubomir
author_facet Gąsowska-Bajger, Beata
Gąsowska-Bodnar, Agnieszka
Knapp, Paweł
Bodnar, Lubomir
author_sort Gąsowska-Bajger, Beata
collection PubMed
description Background: Survivin belongs to the protein family of inhibitors of apoptosis (IAP) and is a regulator of the cell cycle and apoptosis. The aim of this study was to assess the clinical and prognostic significance of expression survivin in patients with ovarian cancer. Methods: We systematically searched for articles in PubMed, the American Chemical Society (Publications), Medline, the Royal Society of Chemistry, Scopus and the Web of Science. Patient clinical data, overall survival (OS), disease-free survival (DFS), and survivin expression were extracted from individual studies. We performed statistical analysis using the STATA 16 package. Eighteen publications containing data from 2233 patients with ovarian cancer were included in this meta-analysis. Results: We found an adverse effect of survivin expression on OS (risk ratio (HR): 1.60; 95% confidence interval (CI): 1.33–1.93, p = 0.00) but this was not observed on DFS (HR: 1.06; 95% CI: 0.55–2.05, p = 0.87). The analysis of clinicopathological parameters showed that survivin expression was associated with the histological grades (G1–2 vs. G3) (odds ratio (OR) = 0.53, 95% CI: 0.34–0.83, p = 0.01) and: International Federation Gynecology and Obstetrics (FIGO) stage (I–II vs. III–IV) (OR = 0.22, 95% CI: 0.09–0.55, p = 0.00), but it was not significantly correlated with the histological subtype (OR = 1.14, 95% CI: 0.83–1.58, p = 0.42). Conclusions: Our meta-analysis suggests that survivin expression may be a marker of poor prognosis in ovarian cancer. Survivin expression was associated with parameters of greater aggressiveness of ovarian cancer. Prospective studies are needed to confirm our results indicating that survivin expression can be used as an ovarian cancer biomarker.
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spelling pubmed-79246012021-03-03 Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis Gąsowska-Bajger, Beata Gąsowska-Bodnar, Agnieszka Knapp, Paweł Bodnar, Lubomir J Clin Med Review Background: Survivin belongs to the protein family of inhibitors of apoptosis (IAP) and is a regulator of the cell cycle and apoptosis. The aim of this study was to assess the clinical and prognostic significance of expression survivin in patients with ovarian cancer. Methods: We systematically searched for articles in PubMed, the American Chemical Society (Publications), Medline, the Royal Society of Chemistry, Scopus and the Web of Science. Patient clinical data, overall survival (OS), disease-free survival (DFS), and survivin expression were extracted from individual studies. We performed statistical analysis using the STATA 16 package. Eighteen publications containing data from 2233 patients with ovarian cancer were included in this meta-analysis. Results: We found an adverse effect of survivin expression on OS (risk ratio (HR): 1.60; 95% confidence interval (CI): 1.33–1.93, p = 0.00) but this was not observed on DFS (HR: 1.06; 95% CI: 0.55–2.05, p = 0.87). The analysis of clinicopathological parameters showed that survivin expression was associated with the histological grades (G1–2 vs. G3) (odds ratio (OR) = 0.53, 95% CI: 0.34–0.83, p = 0.01) and: International Federation Gynecology and Obstetrics (FIGO) stage (I–II vs. III–IV) (OR = 0.22, 95% CI: 0.09–0.55, p = 0.00), but it was not significantly correlated with the histological subtype (OR = 1.14, 95% CI: 0.83–1.58, p = 0.42). Conclusions: Our meta-analysis suggests that survivin expression may be a marker of poor prognosis in ovarian cancer. Survivin expression was associated with parameters of greater aggressiveness of ovarian cancer. Prospective studies are needed to confirm our results indicating that survivin expression can be used as an ovarian cancer biomarker. MDPI 2021-02-21 /pmc/articles/PMC7924601/ /pubmed/33669912 http://dx.doi.org/10.3390/jcm10040879 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Gąsowska-Bajger, Beata
Gąsowska-Bodnar, Agnieszka
Knapp, Paweł
Bodnar, Lubomir
Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis
title Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis
title_full Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis
title_fullStr Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis
title_full_unstemmed Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis
title_short Prognostic Significance of Survivin Expression in Patients with Ovarian Carcinoma: A Meta-Analysis
title_sort prognostic significance of survivin expression in patients with ovarian carcinoma: a meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924601/
https://www.ncbi.nlm.nih.gov/pubmed/33669912
http://dx.doi.org/10.3390/jcm10040879
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