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Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma

BACKGROUND: Mortality is high in patients with esophageal carcinoma as tumors are rarely detected before the disease has progressed to an advanced stage. Here, we sought to isolate cell-free DNA released into the plasma of patients with esophageal carcinoma, to analyze copy number variations of mark...

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Autores principales: Andolfo, Immacolata, Petrosino, Giuseppe, Vecchione, Loredana, De Antonellis, Pasqualino, Capasso, Mario, Montanaro, Donatella, Gemei, Marica, Troncone, Giancarlo, Iolascon, Achille, Orditura, Michele, Ciardiello, Fortunato, De Vita, Fernando, Zollo, Massimo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3094322/
https://www.ncbi.nlm.nih.gov/pubmed/21481261
http://dx.doi.org/10.1186/1471-2407-11-126
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author Andolfo, Immacolata
Petrosino, Giuseppe
Vecchione, Loredana
De Antonellis, Pasqualino
Capasso, Mario
Montanaro, Donatella
Gemei, Marica
Troncone, Giancarlo
Iolascon, Achille
Orditura, Michele
Ciardiello, Fortunato
De Vita, Fernando
Zollo, Massimo
author_facet Andolfo, Immacolata
Petrosino, Giuseppe
Vecchione, Loredana
De Antonellis, Pasqualino
Capasso, Mario
Montanaro, Donatella
Gemei, Marica
Troncone, Giancarlo
Iolascon, Achille
Orditura, Michele
Ciardiello, Fortunato
De Vita, Fernando
Zollo, Massimo
author_sort Andolfo, Immacolata
collection PubMed
description BACKGROUND: Mortality is high in patients with esophageal carcinoma as tumors are rarely detected before the disease has progressed to an advanced stage. Here, we sought to isolate cell-free DNA released into the plasma of patients with esophageal carcinoma, to analyze copy number variations of marker genes in the search for early detection of tumor progression. METHODS: Plasma of 41 patients with esophageal carcinoma was prospectively collected before tumor resection and chemotherapy. Our dataset resulted heterogeneous for clinical data, resembling the characteristics of the tumor. DNA from the plasma was extracted to analyze copy number variations of the erbB2 gene using real-time PCR assays. RESULTS: The real-time PCR assays for erbB2 gene showed significant (P = 0.001) copy number variations in the plasma of patients with esophageal carcinoma, as compared to healthy controls with high sensitivity (80%) and specificity (95%). These variations in erbB2 were negatively correlated to the progression free survival of these patients (P = 0.03), and revealed a further risk category stratification of patients with low VEGF expression levels. CONCLUSION: The copy number variation of erbB2 gene from plasma can be used as prognostic marker for early detection of patients at risk of worse clinical outcome in esophageal cancer.
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spelling pubmed-30943222011-05-14 Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma Andolfo, Immacolata Petrosino, Giuseppe Vecchione, Loredana De Antonellis, Pasqualino Capasso, Mario Montanaro, Donatella Gemei, Marica Troncone, Giancarlo Iolascon, Achille Orditura, Michele Ciardiello, Fortunato De Vita, Fernando Zollo, Massimo BMC Cancer Research Article BACKGROUND: Mortality is high in patients with esophageal carcinoma as tumors are rarely detected before the disease has progressed to an advanced stage. Here, we sought to isolate cell-free DNA released into the plasma of patients with esophageal carcinoma, to analyze copy number variations of marker genes in the search for early detection of tumor progression. METHODS: Plasma of 41 patients with esophageal carcinoma was prospectively collected before tumor resection and chemotherapy. Our dataset resulted heterogeneous for clinical data, resembling the characteristics of the tumor. DNA from the plasma was extracted to analyze copy number variations of the erbB2 gene using real-time PCR assays. RESULTS: The real-time PCR assays for erbB2 gene showed significant (P = 0.001) copy number variations in the plasma of patients with esophageal carcinoma, as compared to healthy controls with high sensitivity (80%) and specificity (95%). These variations in erbB2 were negatively correlated to the progression free survival of these patients (P = 0.03), and revealed a further risk category stratification of patients with low VEGF expression levels. CONCLUSION: The copy number variation of erbB2 gene from plasma can be used as prognostic marker for early detection of patients at risk of worse clinical outcome in esophageal cancer. BioMed Central 2011-04-11 /pmc/articles/PMC3094322/ /pubmed/21481261 http://dx.doi.org/10.1186/1471-2407-11-126 Text en Copyright ©2011 Andolfo 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 Article
Andolfo, Immacolata
Petrosino, Giuseppe
Vecchione, Loredana
De Antonellis, Pasqualino
Capasso, Mario
Montanaro, Donatella
Gemei, Marica
Troncone, Giancarlo
Iolascon, Achille
Orditura, Michele
Ciardiello, Fortunato
De Vita, Fernando
Zollo, Massimo
Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma
title Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma
title_full Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma
title_fullStr Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma
title_full_unstemmed Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma
title_short Detection of erbB2 copy number variations in plasma of patients with esophageal carcinoma
title_sort detection of erbb2 copy number variations in plasma of patients with esophageal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3094322/
https://www.ncbi.nlm.nih.gov/pubmed/21481261
http://dx.doi.org/10.1186/1471-2407-11-126
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