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Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome

BACKGROUND: Adenocarcinomas of the ampulla of Vater are classified as biliary cancers, though the exact epithelium of origin for these cancers is not known. We sought to molecularly classify ampullary adenocarcinomas in comparison to known adenocarcinomas of the pancreas, bile duct, and duodenum by...

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Autores principales: Overman, Michael J., Zhang, Jiexin, Kopetz, Scott, Davies, Michael, Zhi-Qin, Jiang, Stemke-Hale, Katherine, Rümmele, Petra, Pilarsky, Christian, Grützmann, Robert, Hamilton, Stanley, Hwang, Rosa, Abbruzzese, James L., Varadhachary, Gauri, Broom, Bradley, Wang, Huamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679143/
https://www.ncbi.nlm.nih.gov/pubmed/23776447
http://dx.doi.org/10.1371/journal.pone.0065144
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author Overman, Michael J.
Zhang, Jiexin
Kopetz, Scott
Davies, Michael
Zhi-Qin, Jiang
Stemke-Hale, Katherine
Rümmele, Petra
Pilarsky, Christian
Grützmann, Robert
Hamilton, Stanley
Hwang, Rosa
Abbruzzese, James L.
Varadhachary, Gauri
Broom, Bradley
Wang, Huamin
author_facet Overman, Michael J.
Zhang, Jiexin
Kopetz, Scott
Davies, Michael
Zhi-Qin, Jiang
Stemke-Hale, Katherine
Rümmele, Petra
Pilarsky, Christian
Grützmann, Robert
Hamilton, Stanley
Hwang, Rosa
Abbruzzese, James L.
Varadhachary, Gauri
Broom, Bradley
Wang, Huamin
author_sort Overman, Michael J.
collection PubMed
description BACKGROUND: Adenocarcinomas of the ampulla of Vater are classified as biliary cancers, though the exact epithelium of origin for these cancers is not known. We sought to molecularly classify ampullary adenocarcinomas in comparison to known adenocarcinomas of the pancreas, bile duct, and duodenum by gene expression analysis. METHODS: We analyzed 32 fresh-frozen resected, untreated periampullary adenocarcinomas (8 pancreatic, 2 extrahepatic biliary, 8 duodenal, and 14 ampullary) using the Affymetrix U133 Plus 2.0 genome array. Unsupervised and supervised hierarchical clustering identified two subtypes of ampullary carcinomas that were molecularly and histologically characterized. RESULTS: Hierarchical clustering of periampullary carcinomas segregated ampullary carcinomas into two subgroups, which were distinctly different from pancreatic carcinomas. Non-pancreatic periampullary adenocarcinomas were segregated into two subgroups with differing prognoses: 5 year RFS (77% vs. 0%, p = 0.007) and 5 year OS (100% vs. 35%, p = 0.005). Unsupervised clustering analysis of the 14 ampullary samples also identified two subgroups: a good prognosis intestinal-like subgroup and a poor prognosis biliary-like subgroup with 5 year OS of 70% vs. 28%, P = 0.09. Expression of CK7+/CK20- but not CDX-2 correlated with these two subgroups. Activation of the AKT and MAPK pathways were both increased in the poor prognostic biliary-like subgroup. In an independent 80 patient ampullary validation dataset only histological subtype (intestinal vs. pancreaticobiliary) was significantly associated with OS in both univariate (p = 0.006) and multivariate analysis (P = 0.04). CONCLUSIONS: Gene expression analysis discriminated pancreatic adenocarcinomas from other periampullary carcinomas and identified two prognostically relevant subgroups of ampullary adenocarcinomas. Histological subtype was an independent prognostic factor in ampullary adenocarcinomas.
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spelling pubmed-36791432013-06-17 Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome Overman, Michael J. Zhang, Jiexin Kopetz, Scott Davies, Michael Zhi-Qin, Jiang Stemke-Hale, Katherine Rümmele, Petra Pilarsky, Christian Grützmann, Robert Hamilton, Stanley Hwang, Rosa Abbruzzese, James L. Varadhachary, Gauri Broom, Bradley Wang, Huamin PLoS One Research Article BACKGROUND: Adenocarcinomas of the ampulla of Vater are classified as biliary cancers, though the exact epithelium of origin for these cancers is not known. We sought to molecularly classify ampullary adenocarcinomas in comparison to known adenocarcinomas of the pancreas, bile duct, and duodenum by gene expression analysis. METHODS: We analyzed 32 fresh-frozen resected, untreated periampullary adenocarcinomas (8 pancreatic, 2 extrahepatic biliary, 8 duodenal, and 14 ampullary) using the Affymetrix U133 Plus 2.0 genome array. Unsupervised and supervised hierarchical clustering identified two subtypes of ampullary carcinomas that were molecularly and histologically characterized. RESULTS: Hierarchical clustering of periampullary carcinomas segregated ampullary carcinomas into two subgroups, which were distinctly different from pancreatic carcinomas. Non-pancreatic periampullary adenocarcinomas were segregated into two subgroups with differing prognoses: 5 year RFS (77% vs. 0%, p = 0.007) and 5 year OS (100% vs. 35%, p = 0.005). Unsupervised clustering analysis of the 14 ampullary samples also identified two subgroups: a good prognosis intestinal-like subgroup and a poor prognosis biliary-like subgroup with 5 year OS of 70% vs. 28%, P = 0.09. Expression of CK7+/CK20- but not CDX-2 correlated with these two subgroups. Activation of the AKT and MAPK pathways were both increased in the poor prognostic biliary-like subgroup. In an independent 80 patient ampullary validation dataset only histological subtype (intestinal vs. pancreaticobiliary) was significantly associated with OS in both univariate (p = 0.006) and multivariate analysis (P = 0.04). CONCLUSIONS: Gene expression analysis discriminated pancreatic adenocarcinomas from other periampullary carcinomas and identified two prognostically relevant subgroups of ampullary adenocarcinomas. Histological subtype was an independent prognostic factor in ampullary adenocarcinomas. Public Library of Science 2013-06-11 /pmc/articles/PMC3679143/ /pubmed/23776447 http://dx.doi.org/10.1371/journal.pone.0065144 Text en © 2013 Overman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Overman, Michael J.
Zhang, Jiexin
Kopetz, Scott
Davies, Michael
Zhi-Qin, Jiang
Stemke-Hale, Katherine
Rümmele, Petra
Pilarsky, Christian
Grützmann, Robert
Hamilton, Stanley
Hwang, Rosa
Abbruzzese, James L.
Varadhachary, Gauri
Broom, Bradley
Wang, Huamin
Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome
title Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome
title_full Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome
title_fullStr Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome
title_full_unstemmed Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome
title_short Gene Expression Profiling of Ampullary Carcinomas Classifies Ampullary Carcinomas into Biliary-Like and Intestinal-Like Subtypes That Are Prognostic of Outcome
title_sort gene expression profiling of ampullary carcinomas classifies ampullary carcinomas into biliary-like and intestinal-like subtypes that are prognostic of outcome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679143/
https://www.ncbi.nlm.nih.gov/pubmed/23776447
http://dx.doi.org/10.1371/journal.pone.0065144
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