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 in | European journal of human genetics : EJHG Vol. 19; no. 1; pp. 118 - 120 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.01.2011
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1018-4813 1476-5438 1476-5438 |
DOI | 10.1038/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. |
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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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CitedBy_id | crossref_primary_10_1007_s00439_015_1542_9 crossref_primary_10_1111_j_1464_410X_2012_11236_x crossref_primary_10_1134_S0026893312020124 crossref_primary_10_4238_2013_March_15_2 crossref_primary_10_1007_s00247_012_2428_9 crossref_primary_10_7314_APJCP_2012_13_12_6055 crossref_primary_10_1038_pcan_2013_9 crossref_primary_10_1016_j_juro_2011_09_011 crossref_primary_10_7314_APJCP_2013_14_11_6733 crossref_primary_10_1007_s12253_013_9617_1 crossref_primary_10_1038_srep12069 crossref_primary_10_3389_fphys_2018_00915 crossref_primary_10_7314_APJCP_2014_15_19_8311 crossref_primary_10_1097_MD_0000000000020716 crossref_primary_10_1007_s10689_013_9673_4 |
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DocumentTitleAlternate | 8q24 and prostate cancer |
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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 |
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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 |
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