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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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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. |
format | Text |
id | pubmed-3094322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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