Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>

<p>Abstract</p> <p>Background</p> <p>Previous results have suggested an association of the region of 19q13.3 with several forms of cancer. In the present study, we investigated 27 public markers within a previously identified 69 kb stretch of chromosome 19q for associat...

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Main Authors: Mains Mette, Hansen Bettina, Koca Cemile, Zhang Xiuqing, Rockenbauer Eszter, Bukowy Zuzanna, Nyegaard Mette, Olsen Anja, Vogel Ulla, Nexø Bjørn A, Hedemand Anne, Kjeldgaard Anette, Laska Magdalena J, Raaschou-Nielsen Ole, Cold Søren, Overvad Kim, Tjønneland Anne, Bolund Lars, Børglum Anders D
Format: Article
Language:English
Published: BMC 2008-06-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/9/56
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spelling doaj-76f00bb87ee74f14ae1c93209e5be6812021-04-02T16:33:44ZengBMCBMC Medical Genetics1471-23502008-06-01915610.1186/1471-2350-9-56Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>Mains MetteHansen BettinaKoca CemileZhang XiuqingRockenbauer EszterBukowy ZuzannaNyegaard MetteOlsen AnjaVogel UllaNexø Bjørn AHedemand AnneKjeldgaard AnetteLaska Magdalena JRaaschou-Nielsen OleCold SørenOvervad KimTjønneland AnneBolund LarsBørglum Anders D<p>Abstract</p> <p>Background</p> <p>Previous results have suggested an association of the region of 19q13.3 with several forms of cancer. In the present study, we investigated 27 public markers within a previously identified 69 kb stretch of chromosome 19q for association with breast cancer by using linkage disequilibrium mapping. The study groups included 434 postmenopausal breast cancer cases and an identical number of individually matched controls.</p> <p>Methods and Results</p> <p>Studying one marker at a time, we found a region spanning the gene <it>RAI </it>(alias <it>PPP1R13L or iASPP</it>) and the 5' portion of <it>XPD </it>to be associated with this cancer. The region corresponds to a haplotype block, in which there seems to be very limited recombination in the Danish population. Studying combinations of markers, we found that two to four neighboring markers gave the most consistent and strongest result. The haplotypes with strongest association with cancers were located in the gene <it>RAI </it>and just 3' to the gene. Coinciding peaks were seen in the region of <it>RAI </it>in groups of women of different age.</p> <p>In a follow-up to these results we sequenced 10 cases and 10 controls in a 44 kb region spanning the peaks of association. This revealed 106 polymorphisms, many of which were not in the public databases. We tested an additional 44 of these for association with disease and found a new tandem repeat marker, called <it>RAI</it>-3'd1, located downstream of the transcribed region of <it>RAI</it>, which was more strongly associated with breast cancer than any other marker we have tested (RR = 2.44 (1.41–4.23, p = 0.0008, all cases; RR = 6.29 (1.49–26.6), p = 0.01, cases up to 55 years of age).</p> <p>Conclusion</p> <p>We expect the marker <it>RAI</it>-3'd1 to be (part of) the cause for the association of the chromosome 19q13.3 region's association with cancer.</p> http://www.biomedcentral.com/1471-2350/9/56
collection DOAJ
language English
format Article
sources DOAJ
author Mains Mette
Hansen Bettina
Koca Cemile
Zhang Xiuqing
Rockenbauer Eszter
Bukowy Zuzanna
Nyegaard Mette
Olsen Anja
Vogel Ulla
Nexø Bjørn A
Hedemand Anne
Kjeldgaard Anette
Laska Magdalena J
Raaschou-Nielsen Ole
Cold Søren
Overvad Kim
Tjønneland Anne
Bolund Lars
Børglum Anders D
spellingShingle Mains Mette
Hansen Bettina
Koca Cemile
Zhang Xiuqing
Rockenbauer Eszter
Bukowy Zuzanna
Nyegaard Mette
Olsen Anja
Vogel Ulla
Nexø Bjørn A
Hedemand Anne
Kjeldgaard Anette
Laska Magdalena J
Raaschou-Nielsen Ole
Cold Søren
Overvad Kim
Tjønneland Anne
Bolund Lars
Børglum Anders D
Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>
BMC Medical Genetics
author_facet Mains Mette
Hansen Bettina
Koca Cemile
Zhang Xiuqing
Rockenbauer Eszter
Bukowy Zuzanna
Nyegaard Mette
Olsen Anja
Vogel Ulla
Nexø Bjørn A
Hedemand Anne
Kjeldgaard Anette
Laska Magdalena J
Raaschou-Nielsen Ole
Cold Søren
Overvad Kim
Tjønneland Anne
Bolund Lars
Børglum Anders D
author_sort Mains Mette
title Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>
title_short Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>
title_full Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>
title_fullStr Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>
title_full_unstemmed Linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>RAI/PPP1R13L/iASPP</it>
title_sort linkage disequilibrium mapping of a breast cancer susceptibility locus near <it>rai/ppp1r13l/iaspp</it>
publisher BMC
series BMC Medical Genetics
issn 1471-2350
publishDate 2008-06-01
description <p>Abstract</p> <p>Background</p> <p>Previous results have suggested an association of the region of 19q13.3 with several forms of cancer. In the present study, we investigated 27 public markers within a previously identified 69 kb stretch of chromosome 19q for association with breast cancer by using linkage disequilibrium mapping. The study groups included 434 postmenopausal breast cancer cases and an identical number of individually matched controls.</p> <p>Methods and Results</p> <p>Studying one marker at a time, we found a region spanning the gene <it>RAI </it>(alias <it>PPP1R13L or iASPP</it>) and the 5' portion of <it>XPD </it>to be associated with this cancer. The region corresponds to a haplotype block, in which there seems to be very limited recombination in the Danish population. Studying combinations of markers, we found that two to four neighboring markers gave the most consistent and strongest result. The haplotypes with strongest association with cancers were located in the gene <it>RAI </it>and just 3' to the gene. Coinciding peaks were seen in the region of <it>RAI </it>in groups of women of different age.</p> <p>In a follow-up to these results we sequenced 10 cases and 10 controls in a 44 kb region spanning the peaks of association. This revealed 106 polymorphisms, many of which were not in the public databases. We tested an additional 44 of these for association with disease and found a new tandem repeat marker, called <it>RAI</it>-3'd1, located downstream of the transcribed region of <it>RAI</it>, which was more strongly associated with breast cancer than any other marker we have tested (RR = 2.44 (1.41–4.23, p = 0.0008, all cases; RR = 6.29 (1.49–26.6), p = 0.01, cases up to 55 years of age).</p> <p>Conclusion</p> <p>We expect the marker <it>RAI</it>-3'd1 to be (part of) the cause for the association of the chromosome 19q13.3 region's association with cancer.</p>
url http://www.biomedcentral.com/1471-2350/9/56
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