Gastric cancers of Western European and African patients show different patterns of genomic instability

<p>Abstract</p> <p>Background</p> <p>Infection with <it>H. pylori </it>is important in the etiology of gastric cancer. Gastric cancer is infrequent in Africa, despite high frequencies of <it>H. pylori </it>infection, referred to as the African en...

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Main Authors: Mulder Chris JJ, Grabsch Heike, Ylstra Bauke, Carvalho Beatriz, Tijssen Marianne, van Grieken Nicole CT, Louw Melanie, Buffart Tineke E, van de Velde Cornelis JH, van der Merwe Schalk W, Meijer Gerrit A
Format: Article
Language:English
Published: BMC 2011-01-01
Series:BMC Medical Genomics
Online Access:http://www.biomedcentral.com/1755-8794/4/7
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spelling doaj-01940b618bde452fbb3edc4d9351843b2021-04-02T13:42:07ZengBMCBMC Medical Genomics1755-87942011-01-0141710.1186/1755-8794-4-7Gastric cancers of Western European and African patients show different patterns of genomic instabilityMulder Chris JJGrabsch HeikeYlstra BaukeCarvalho BeatrizTijssen Mariannevan Grieken Nicole CTLouw MelanieBuffart Tineke Evan de Velde Cornelis JHvan der Merwe Schalk WMeijer Gerrit A<p>Abstract</p> <p>Background</p> <p>Infection with <it>H. pylori </it>is important in the etiology of gastric cancer. Gastric cancer is infrequent in Africa, despite high frequencies of <it>H. pylori </it>infection, referred to as the African enigma. Variation in environmental and host factors influencing gastric cancer risk between different populations have been reported but little is known about the biological differences between gastric cancers from different geographic locations. We aim to study genomic instability patterns of gastric cancers obtained from patients from United Kingdom (UK) and South Africa (SA), in an attempt to support the African enigma hypothesis at the biological level.</p> <p>Methods</p> <p>DNA was isolated from 67 gastric adenocarcinomas, 33 UK patients, 9 Caucasian SA patients and 25 native SA patients. Microsatellite instability and chromosomal instability were analyzed by PCR and microarray comparative genomic hybridization, respectively. Data was analyzed by supervised univariate and multivariate analyses as well as unsupervised hierarchical cluster analysis.</p> <p>Results</p> <p>Tumors from Caucasian and native SA patients showed significantly more microsatellite instable tumors (p < 0.05). For the microsatellite stable tumors, geographical origin of the patients correlated with cluster membership, derived from unsupervised hierarchical cluster analysis (p = 0.001). Several chromosomal alterations showed significantly different frequencies in tumors from UK patients and native SA patients, but not between UK and Caucasian SA patients and between native and Caucasian SA patients.</p> <p>Conclusions</p> <p>Gastric cancers from SA and UK patients show differences in genetic instability patterns, indicating possible different biological mechanisms in patients from different geographical origin. This is of future clinical relevance for stratification of gastric cancer therapy.</p> http://www.biomedcentral.com/1755-8794/4/7
collection DOAJ
language English
format Article
sources DOAJ
author Mulder Chris JJ
Grabsch Heike
Ylstra Bauke
Carvalho Beatriz
Tijssen Marianne
van Grieken Nicole CT
Louw Melanie
Buffart Tineke E
van de Velde Cornelis JH
van der Merwe Schalk W
Meijer Gerrit A
spellingShingle Mulder Chris JJ
Grabsch Heike
Ylstra Bauke
Carvalho Beatriz
Tijssen Marianne
van Grieken Nicole CT
Louw Melanie
Buffart Tineke E
van de Velde Cornelis JH
van der Merwe Schalk W
Meijer Gerrit A
Gastric cancers of Western European and African patients show different patterns of genomic instability
BMC Medical Genomics
author_facet Mulder Chris JJ
Grabsch Heike
Ylstra Bauke
Carvalho Beatriz
Tijssen Marianne
van Grieken Nicole CT
Louw Melanie
Buffart Tineke E
van de Velde Cornelis JH
van der Merwe Schalk W
Meijer Gerrit A
author_sort Mulder Chris JJ
title Gastric cancers of Western European and African patients show different patterns of genomic instability
title_short Gastric cancers of Western European and African patients show different patterns of genomic instability
title_full Gastric cancers of Western European and African patients show different patterns of genomic instability
title_fullStr Gastric cancers of Western European and African patients show different patterns of genomic instability
title_full_unstemmed Gastric cancers of Western European and African patients show different patterns of genomic instability
title_sort gastric cancers of western european and african patients show different patterns of genomic instability
publisher BMC
series BMC Medical Genomics
issn 1755-8794
publishDate 2011-01-01
description <p>Abstract</p> <p>Background</p> <p>Infection with <it>H. pylori </it>is important in the etiology of gastric cancer. Gastric cancer is infrequent in Africa, despite high frequencies of <it>H. pylori </it>infection, referred to as the African enigma. Variation in environmental and host factors influencing gastric cancer risk between different populations have been reported but little is known about the biological differences between gastric cancers from different geographic locations. We aim to study genomic instability patterns of gastric cancers obtained from patients from United Kingdom (UK) and South Africa (SA), in an attempt to support the African enigma hypothesis at the biological level.</p> <p>Methods</p> <p>DNA was isolated from 67 gastric adenocarcinomas, 33 UK patients, 9 Caucasian SA patients and 25 native SA patients. Microsatellite instability and chromosomal instability were analyzed by PCR and microarray comparative genomic hybridization, respectively. Data was analyzed by supervised univariate and multivariate analyses as well as unsupervised hierarchical cluster analysis.</p> <p>Results</p> <p>Tumors from Caucasian and native SA patients showed significantly more microsatellite instable tumors (p < 0.05). For the microsatellite stable tumors, geographical origin of the patients correlated with cluster membership, derived from unsupervised hierarchical cluster analysis (p = 0.001). Several chromosomal alterations showed significantly different frequencies in tumors from UK patients and native SA patients, but not between UK and Caucasian SA patients and between native and Caucasian SA patients.</p> <p>Conclusions</p> <p>Gastric cancers from SA and UK patients show differences in genetic instability patterns, indicating possible different biological mechanisms in patients from different geographical origin. This is of future clinical relevance for stratification of gastric cancer therapy.</p>
url http://www.biomedcentral.com/1755-8794/4/7
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