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Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival

BACKGROUND: The detection of circulating tumor cells (CTC) is considered a promising tool for improving risk stratification in patients with solid tumors. We investigated on whether the expression of CTC related genes adds any prognostic power to the TNM staging system in patients with gastric carci...

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Autores principales: Bertazza, Loris, Mocellin, Simone, Marchet, Alberto, Pilati, Pierluigi, Gabrieli, Joseph, Scalerta, Romano, Nitti, Donato
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807427/
https://www.ncbi.nlm.nih.gov/pubmed/20028510
http://dx.doi.org/10.1186/1479-5876-7-111
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author Bertazza, Loris
Mocellin, Simone
Marchet, Alberto
Pilati, Pierluigi
Gabrieli, Joseph
Scalerta, Romano
Nitti, Donato
author_facet Bertazza, Loris
Mocellin, Simone
Marchet, Alberto
Pilati, Pierluigi
Gabrieli, Joseph
Scalerta, Romano
Nitti, Donato
author_sort Bertazza, Loris
collection PubMed
description BACKGROUND: The detection of circulating tumor cells (CTC) is considered a promising tool for improving risk stratification in patients with solid tumors. We investigated on whether the expression of CTC related genes adds any prognostic power to the TNM staging system in patients with gastric carcinoma. METHODS: Seventy patients with TNM stage I to IV gastric carcinoma were retrospectively enrolled. Peripheral blood samples were tested by means of quantitative real time PCR (qrtPCR) for the expression of four CTC related genes: carcinoembryonic antigen (CEA), cytokeratin-19 (CK19), vascular endothelial growth factor (VEGF) and Survivin (BIRC5). RESULTS: Gene expression of Survivin, CK19, CEA and VEGF was higher than in normal controls in 98.6%, 97.1%, 42.9% and 38.6% of cases, respectively, suggesting a potential diagnostic value of both Survivin and CK19. At multivariable survival analysis, TNM staging and Survivin mRNA levels were retained as independent prognostic factors, demonstrating that Survivin expression in the peripheral blood adds prognostic information to the TNM system. In contrast with previously published data, the transcript abundance of CEA, CK19 and VEGF was not associated with patients' clinical outcome. CONCLUSIONS: Gene expression levels of Survivin add significant prognostic value to the current TNM staging system. The validation of these findings in larger prospective and multicentric series might lead to the implementation of this biomarker in the routine clinical setting in order to optimize risk stratification and ultimately personalize the therapeutic management of these patients.
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spelling pubmed-28074272010-01-16 Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival Bertazza, Loris Mocellin, Simone Marchet, Alberto Pilati, Pierluigi Gabrieli, Joseph Scalerta, Romano Nitti, Donato J Transl Med Research BACKGROUND: The detection of circulating tumor cells (CTC) is considered a promising tool for improving risk stratification in patients with solid tumors. We investigated on whether the expression of CTC related genes adds any prognostic power to the TNM staging system in patients with gastric carcinoma. METHODS: Seventy patients with TNM stage I to IV gastric carcinoma were retrospectively enrolled. Peripheral blood samples were tested by means of quantitative real time PCR (qrtPCR) for the expression of four CTC related genes: carcinoembryonic antigen (CEA), cytokeratin-19 (CK19), vascular endothelial growth factor (VEGF) and Survivin (BIRC5). RESULTS: Gene expression of Survivin, CK19, CEA and VEGF was higher than in normal controls in 98.6%, 97.1%, 42.9% and 38.6% of cases, respectively, suggesting a potential diagnostic value of both Survivin and CK19. At multivariable survival analysis, TNM staging and Survivin mRNA levels were retained as independent prognostic factors, demonstrating that Survivin expression in the peripheral blood adds prognostic information to the TNM system. In contrast with previously published data, the transcript abundance of CEA, CK19 and VEGF was not associated with patients' clinical outcome. CONCLUSIONS: Gene expression levels of Survivin add significant prognostic value to the current TNM staging system. The validation of these findings in larger prospective and multicentric series might lead to the implementation of this biomarker in the routine clinical setting in order to optimize risk stratification and ultimately personalize the therapeutic management of these patients. BioMed Central 2009-12-22 /pmc/articles/PMC2807427/ /pubmed/20028510 http://dx.doi.org/10.1186/1479-5876-7-111 Text en Copyright ©2009 Bertazza et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Bertazza, Loris
Mocellin, Simone
Marchet, Alberto
Pilati, Pierluigi
Gabrieli, Joseph
Scalerta, Romano
Nitti, Donato
Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
title Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
title_full Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
title_fullStr Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
title_full_unstemmed Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
title_short Survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
title_sort survivin gene levels in the peripheral blood of patients with gastric cancer independently predict survival
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807427/
https://www.ncbi.nlm.nih.gov/pubmed/20028510
http://dx.doi.org/10.1186/1479-5876-7-111
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