Genetic marker polymorphisms on chromosome 8q24 and prostate cancer in the Dutch population: DG8S737 may not be the causative variant

Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SN...

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Published inEuropean journal of human genetics : EJHG Vol. 19; no. 1; pp. 118 - 120
Main Authors Zeegers, Maurice P, Khan, Humera S, Schouten, Leo J, van Dijk, Boukje A C, Goldbohm, R Alexandra, Schalken, Jack, Shajahan, Shahin, Pearlman, Alexander, Oddoux, Carole, van den Brandt, Piet A, Ostrer, Harry
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.01.2011
Nature Publishing Group
Subjects
SNP
Online AccessGet full text
ISSN1018-4813
1476-5438
1476-5438
DOI10.1038/ejhg.2010.133

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Abstract Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As GWAS are subjected to type 1 error, confirmation studies are required to validate the results. Here, we analysed the same markers in 277 cases and 282 controls from the Netherlands using a nested case–control study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study. We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele ( P =0.10), although the effect estimate was in the same direction as previous studies (odds ratio (OR), 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P =0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high-risk haplotype present in the Caucasian population. This short report highlights the importance of validation, although further confirmation is still needed.
AbstractList Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As GWAS are subjected to type 1 error, confirmation studies are required to validate the results. Here, we analysed the same markers in 277 cases and 282 controls from the Netherlands using a nested caseacontrol study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study. We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele (P=0.10), although the effect estimate was in the same direction as previous studies (odds ratio (OR), 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P=0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high-risk haplotype present in the Caucasian population. This short report highlights the importance of validation, although further confirmation is still needed.
Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As GWAS are subjected to type 1 error, confirmation studies are required to validate the results. Here, we analysed the same markers in 277 cases and 282 controls from the Netherlands using a nested case-control study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study. We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele (P=0.10), although the effect estimate was in the same direction as previous studies (odds ratio (OR), 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P=0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high-risk haplotype present in the Caucasian population. This short report highlights the importance of validation, although further confirmation is still needed.Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As GWAS are subjected to type 1 error, confirmation studies are required to validate the results. Here, we analysed the same markers in 277 cases and 282 controls from the Netherlands using a nested case-control study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study. We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele (P=0.10), although the effect estimate was in the same direction as previous studies (odds ratio (OR), 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P=0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high-risk haplotype present in the Caucasian population. This short report highlights the importance of validation, although further confirmation is still needed.
Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Whole genome association (WGA) studies have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As WGA studies are subject to type 1 error, confirmation studies are required to validate the results. Here, we analyzed the same markers in 277 cases and 282 controls from the Netherlands using a nested case control study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study (NLCS). We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele (P=0.10) although the effect estimate was in the same direction as previous studies (OR, 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P=0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high risk haplotype present in the Caucasian population. The short report highlights the importance of validation although further confirmation is still needed.
Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As GWAS are subjected to type 1 error, confirmation studies are required to validate the results. Here, we analysed the same markers in 277 cases and 282 controls from the Netherlands using a nested case-control study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study. We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele (P=0.10), although the effect estimate was in the same direction as previous studies (odds ratio (OR), 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P=0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high-risk haplotype present in the Caucasian population. This short report highlights the importance of validation, although further confirmation is still needed.
Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an association with markers on chromosome 8q24. Allele -8 of microsatellite DG8S737 with 22 repeats and allele A of the single-nucleotide polymorphism (SNP) rs1447295 have been found to be significantly associated with prostate cancer. As GWAS are subjected to type 1 error, confirmation studies are required to validate the results. Here, we analysed the same markers in 277 cases and 282 controls from the Netherlands using a nested case–control study. Incident prostate cancer cases and controls selected were identified in the population of the Netherlands Cohort Study. We also investigated clinical features of the disease by stratifying by tumour stage. We did not replicate the association with the SNP rs1447295-A allele ( P =0.10), although the effect estimate was in the same direction as previous studies (odds ratio (OR), 1.38). Interestingly a statistically significant decreased risk was observed for DG8S737 allele -8 (OR, 0.62; P =0.03). The apparent protective effect of the DG8S737 -8 allele observed in this study contrasts with the Amundadottir study. This suggests that DG8S737 and rs1447295 might be tightly linked markers flanking the actual causative variant and that there may be potentially more than one high-risk haplotype present in the Caucasian population. This short report highlights the importance of validation, although further confirmation is still needed.
Author van Dijk, Boukje A C
Pearlman, Alexander
van den Brandt, Piet A
Ostrer, Harry
Oddoux, Carole
Shajahan, Shahin
Zeegers, Maurice P
Schalken, Jack
Khan, Humera S
Schouten, Leo J
Goldbohm, R Alexandra
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Cites_doi 10.1038/ng1808
10.1158/1055-9965.EPI-06-1049
10.1016/S0379-0738(02)00194-9
10.1158/0008-5472.CAN-06-3186
10.1002/(SICI)1097-0142(19971101)80:9<1803::AID-CNCR16>3.0.CO;2-9
10.3322/caac.20006
10.1038/ng1999
10.1038/sj.ejhg.5201151
10.1016/0895-4356(90)90009-E
10.1007/s00439-007-0448-6
10.1038/ng2022
10.1093/genetics/155.2.945
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Issue 1
Keywords epidemiology
cancer
prostatic neoplasm/genetics
SNP
microsatellite repeats/genetics
Chromosomal aberration
Genetic mapping
Human
Prostate tumor
Urinary system disease
Prostate disease
Genetic marker
Repeated sequence
Aneuploidy
Malignant tumor
Epidemiology
Variant
Microsatellite DNA
Supernumerary chromosome
Genetics
Population
Single nucleotide polymorphism
Male genital diseases
Prostate cancer
Dutch
Cancer
prostatic neoplasms/genetics
microsatellite/SNP/genetics
Language English
License http://www.springer.com/tdm
CC BY 4.0
Distributed under a Creative Commons Attribution 4.0 International License: http://creativecommons.org/licenses/by/4.0
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These authors contributed equally to this work.
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References LH Sobin (BFejhg2010133_CR8) 1997; 80
M Suuriniemi (BFejhg2010133_CR3) 2007; 16
L Wang (BFejhg2010133_CR12) 2007; 67
A Jemal (BFejhg2010133_CR1) 2009; 59
MP Zeegers (BFejhg2010133_CR6) 2004; 12
M Yeager (BFejhg2010133_CR4) 2007; 39
PA van den Brandt (BFejhg2010133_CR7) 1990; 43
J Gudmundsson (BFejhg2010133_CR5) 2007; 39
S Ebrahim (BFejhg2010133_CR9) 2008; 123
JKSM Pritchard (BFejhg2010133_CR11) 2000; 155
NKV Sarkar (BFejhg2010133_CR10) 2002; 128
LT Amundadottir (BFejhg2010133_CR2) 2006; 38
17409399 - Cancer Res. 2007 Apr 1;67(7):2944-50
16682969 - Nat Genet. 2006 Jun;38(6):652-8
17401363 - Nat Genet. 2007 May;39(5):645-9
12175966 - Forensic Sci Int. 2002 Aug 28;128(3):196-201
17401366 - Nat Genet. 2007 May;39(5):631-7
18038153 - Hum Genet. 2008 Feb;123(1):15-33
2313318 - J Clin Epidemiol. 1990;43(3):285-95
19474385 - CA Cancer J Clin. 2009 Jul-Aug;59(4):225-49
10835412 - Genetics. 2000 Jun;155(2):945-59
15010701 - Eur J Hum Genet. 2004 Jul;12(7):591-600
9351551 - Cancer. 1997 Nov 1;80(9):1803-4
17416775 - Cancer Epidemiol Biomarkers Prev. 2007 Apr;16(4):809-14
References_xml – volume: 38
  start-page: 652
  year: 2006
  ident: BFejhg2010133_CR2
  publication-title: Nat Genet
  doi: 10.1038/ng1808
– volume: 16
  start-page: 809
  year: 2007
  ident: BFejhg2010133_CR3
  publication-title: Cancer Epidemiol Biomarkers Prev
  doi: 10.1158/1055-9965.EPI-06-1049
– volume: 128
  start-page: 196
  year: 2002
  ident: BFejhg2010133_CR10
  publication-title: Forensic Science International
  doi: 10.1016/S0379-0738(02)00194-9
– volume: 67
  start-page: 2944
  year: 2007
  ident: BFejhg2010133_CR12
  publication-title: Cancer Res
  doi: 10.1158/0008-5472.CAN-06-3186
– volume: 80
  start-page: 1803
  year: 1997
  ident: BFejhg2010133_CR8
  publication-title: Cancer
  doi: 10.1002/(SICI)1097-0142(19971101)80:9<1803::AID-CNCR16>3.0.CO;2-9
– volume: 59
  start-page: 225
  year: 2009
  ident: BFejhg2010133_CR1
  publication-title: CA Cancer J Clin
  doi: 10.3322/caac.20006
– volume: 39
  start-page: 631
  year: 2007
  ident: BFejhg2010133_CR5
  publication-title: Nat Genet
  doi: 10.1038/ng1999
– volume: 12
  start-page: 591
  year: 2004
  ident: BFejhg2010133_CR6
  publication-title: Eur J Hum Genet
  doi: 10.1038/sj.ejhg.5201151
– volume: 43
  start-page: 285
  year: 1990
  ident: BFejhg2010133_CR7
  publication-title: J Clin Epidemiol
  doi: 10.1016/0895-4356(90)90009-E
– volume: 123
  start-page: 15
  year: 2008
  ident: BFejhg2010133_CR9
  publication-title: Hum Genet
  doi: 10.1007/s00439-007-0448-6
– volume: 39
  start-page: 645
  year: 2007
  ident: BFejhg2010133_CR4
  publication-title: Nat Genet
  doi: 10.1038/ng2022
– volume: 155
  start-page: 945
  year: 2000
  ident: BFejhg2010133_CR11
  publication-title: Genetics
  doi: 10.1093/genetics/155.2.945
– reference: 17409399 - Cancer Res. 2007 Apr 1;67(7):2944-50
– reference: 17416775 - Cancer Epidemiol Biomarkers Prev. 2007 Apr;16(4):809-14
– reference: 10835412 - Genetics. 2000 Jun;155(2):945-59
– reference: 9351551 - Cancer. 1997 Nov 1;80(9):1803-4
– reference: 16682969 - Nat Genet. 2006 Jun;38(6):652-8
– reference: 18038153 - Hum Genet. 2008 Feb;123(1):15-33
– reference: 17401366 - Nat Genet. 2007 May;39(5):631-7
– reference: 19474385 - CA Cancer J Clin. 2009 Jul-Aug;59(4):225-49
– reference: 15010701 - Eur J Hum Genet. 2004 Jul;12(7):591-600
– reference: 12175966 - Forensic Sci Int. 2002 Aug 28;128(3):196-201
– reference: 2313318 - J Clin Epidemiol. 1990;43(3):285-95
– reference: 17401363 - Nat Genet. 2007 May;39(5):645-9
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Snippet Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Genome-wide association studies (GWAS) have detected an...
Prostate cancer is the most commonly diagnosed cancer in men in Europe and Northern America. Whole genome association (WGA) studies have detected an...
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SubjectTerms 631/208/2489/144/68
631/208/721
692/699/67/589/466
Alleles
Bioinformatics
Biological and medical sciences
Biomedical and Life Sciences
Biomedicine
Case-Control Studies
Chromosome 8
Chromosomes
Chromosomes, Human, Pair 8 - genetics
Classical genetics, quantitative genetics, hybrids
Cytogenetics
Epidemiology
European Continental Ancestry Group - genetics
Fundamental and applied biological sciences. Psychology
Gene Expression
General aspects. Genetic counseling
Genetic diversity
Genetic markers
Genetic Predisposition to Disease
Genetics of eukaryotes. Biological and molecular evolution
Genomes
Haplotypes
Health risk assessment
Human
Human Genetics
Humans
Male
Medical genetics
Medical sciences
Microsatellite Repeats - genetics
Middle Aged
Molecular and cellular biology
Mutation
Nephrology. Urinary tract diseases
Netherlands
Polymorphism, Genetic
Population
Prostate
Prostate cancer
Prostatic Neoplasms - genetics
Prostatic Neoplasms - pathology
Public health
Risk groups
Short Report
Single-nucleotide polymorphism
Statistical analysis
Studies
Tumors
Tumors of the urinary system
Urinary tract. Prostate gland
White people
Title Genetic marker polymorphisms on chromosome 8q24 and prostate cancer in the Dutch population: DG8S737 may not be the causative variant
URI https://link.springer.com/article/10.1038/ejhg.2010.133
https://www.ncbi.nlm.nih.gov/pubmed/20700145
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https://www.proquest.com/docview/821594761
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https://pubmed.ncbi.nlm.nih.gov/PMC3039500
Volume 19
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