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Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade
BACKGROUND: Oesophageal adenocarcinoma or Barrett's adenocarcinoma (EAC) is increasing in incidence and stratification of prognosis might improve disease management. Multi-colour Fluorescence in situ hybridisation (FISH) investigating ERBB2, MYC, CDKN2A and ZNF217 has recently shown promising r...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056055/ https://www.ncbi.nlm.nih.gov/pubmed/24853183 http://dx.doi.org/10.1038/bjc.2014.238 |
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author | Geppert, C-I Rümmele, P Sarbia, M Langer, R Feith, M Morrison, L Pestova, E Schneider-Stock, R Hartmann, A Rau, T T |
author_facet | Geppert, C-I Rümmele, P Sarbia, M Langer, R Feith, M Morrison, L Pestova, E Schneider-Stock, R Hartmann, A Rau, T T |
author_sort | Geppert, C-I |
collection | PubMed |
description | BACKGROUND: Oesophageal adenocarcinoma or Barrett's adenocarcinoma (EAC) is increasing in incidence and stratification of prognosis might improve disease management. Multi-colour Fluorescence in situ hybridisation (FISH) investigating ERBB2, MYC, CDKN2A and ZNF217 has recently shown promising results for the diagnosis of dysplasia and cancer using cytological samples. METHODS: To identify markers of prognosis we targeted four selected gene loci using multi-colour FISH applied to a tissue microarray containing 130 EAC samples. Prognostic predictors (P1, P2, P3) based on genomic copy numbers of the four loci were statistically assessed to stratify patients according to overall survival in combination with clinical data. RESULTS: The best stratification into favourable and unfavourable prognoses was shown by P1, percentage of cells with less than two ZNF217 signals; P2, percentage of cells with fewer ERBB2- than ZNF217 signals; and P3, overall ratio of ERBB2-/ZNF217 signals. Median survival times for P1 were 32 vs 73 months, 28 vs 73 months for P2; and 27 vs 65 months for P3. Regarding each tumour grade P2 subdivided patients into distinct prognostic groups independently within each grade, with different median survival times of at least 35 months. CONCLUSIONS: Cell signal number of the ERBB2 and ZNF217 loci showed independence from tumour stage and differentiation grade. The prognostic value of multi-colour FISH-assays is applicable to EAC and is superior to single markers. |
format | Online Article Text |
id | pubmed-4056055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-40560552015-06-10 Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade Geppert, C-I Rümmele, P Sarbia, M Langer, R Feith, M Morrison, L Pestova, E Schneider-Stock, R Hartmann, A Rau, T T Br J Cancer Genetics and Genomics BACKGROUND: Oesophageal adenocarcinoma or Barrett's adenocarcinoma (EAC) is increasing in incidence and stratification of prognosis might improve disease management. Multi-colour Fluorescence in situ hybridisation (FISH) investigating ERBB2, MYC, CDKN2A and ZNF217 has recently shown promising results for the diagnosis of dysplasia and cancer using cytological samples. METHODS: To identify markers of prognosis we targeted four selected gene loci using multi-colour FISH applied to a tissue microarray containing 130 EAC samples. Prognostic predictors (P1, P2, P3) based on genomic copy numbers of the four loci were statistically assessed to stratify patients according to overall survival in combination with clinical data. RESULTS: The best stratification into favourable and unfavourable prognoses was shown by P1, percentage of cells with less than two ZNF217 signals; P2, percentage of cells with fewer ERBB2- than ZNF217 signals; and P3, overall ratio of ERBB2-/ZNF217 signals. Median survival times for P1 were 32 vs 73 months, 28 vs 73 months for P2; and 27 vs 65 months for P3. Regarding each tumour grade P2 subdivided patients into distinct prognostic groups independently within each grade, with different median survival times of at least 35 months. CONCLUSIONS: Cell signal number of the ERBB2 and ZNF217 loci showed independence from tumour stage and differentiation grade. The prognostic value of multi-colour FISH-assays is applicable to EAC and is superior to single markers. Nature Publishing Group 2014-06-10 2014-05-22 /pmc/articles/PMC4056055/ /pubmed/24853183 http://dx.doi.org/10.1038/bjc.2014.238 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Genetics and Genomics Geppert, C-I Rümmele, P Sarbia, M Langer, R Feith, M Morrison, L Pestova, E Schneider-Stock, R Hartmann, A Rau, T T Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
title | Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
title_full | Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
title_fullStr | Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
title_full_unstemmed | Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
title_short | Multi-colour FISH in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
title_sort | multi-colour fish in oesophageal adenocarcinoma—predictors of prognosis independent of stage and grade |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056055/ https://www.ncbi.nlm.nih.gov/pubmed/24853183 http://dx.doi.org/10.1038/bjc.2014.238 |
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