학술논문

PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1
Document Type
article
Author
Jiao, XiangAravidis, ChristosMarikkannu, RajeshwariRantala, JohannaPicelli, SimoneAdamovic, TatjanaLiu, TaoMaguire, PaulaKremeyer, BarbaraLuo, Lipingvon Holst, SusannaKontham, VinaykumarThutkawkorapin, JessadaMargolin, SaraDu, QuanLundin, JohannaMichailidou, KyriakiBolla, Manjeet KWang, QinDennis, JoeLush, MichaelAmbrosone, Christine BAndrulis, Irene LAnton-Culver, HodaAntonenkova, Natalia NArndt, VolkerBeckmann, Matthias WBlomqvist, CarlBlot, WilliamBoeckx, BramBojesen, Stig EBonanni, BernardoBrand, Judith SBrauch, HiltrudBrenner, HermannBroeks, AnnegienBrüning, ThomasBurwinkel, BarbaraCai, QiuyinChang-Claude, JennyCouch, Fergus JCox, AngelaCross, Simon SDeming-Halverson, Sandra LDevilee, Peterdos-Santos-Silva, IsabelDörk, ThiloEriksson, MikaelFasching, Peter AFigueroa, JonineFlesch-Janys, DieterFlyger, HenrikGabrielson, MarikeGarcía-Closas, MontserratGiles, Graham GGonzález-Neira, AnnaGuénel, PascalGuo, QiGündert, MelanieHaiman, Christopher AHallberg, EmilyHamann, UteHarrington, PatriciaHooning, Maartje JHopper, John LHuang, GuanmengqianJakubowska, AnnaJones, Michael EKerin, Michael JKosma, Veli-MattiKristensen, Vessela NLambrechts, DietherLe Marchand, LoicLubinski, JanMannermaa, ArtoMartens, John WMMeindl, AlfonsMilne, Roger LMulligan, Anna MarieNeuhausen, Susan LNevanlinna, HeliPeto, JulianPylkäs, KatriRadice, PaoloRhenius, ValerieSawyer, Elinor JSchmidt, Marjanka KSchmutzler, Rita KSeynaeve, CarolineShah, MitulSimard, JacquesSouthey, Melissa CSwerdlow, Anthony JTruong, ThérèseWendt, CamillaWinqvist, RobertZheng, WeiBenitez, JavierDunning, Alison MPharoah, Paul DP
Source
Oncotarget. 8(61)
Subject
Cancer
Prevention
Breast Cancer
Genetics
Human Genome
Genetic Testing
2.1 Biological and endogenous factors
Aetiology
familial breast cancer
linkage analysis
risk haplotype
sequencing
NBCS Collaborators
kConFab/AOCS Investigators
Oncology and Carcinogenesis
Language
Abstract
Most non-BRCA1/2 breast cancer families have no identified genetic cause. We used linkage and haplotype analyses in familial and sporadic breast cancer cases to identify a susceptibility locus on chromosome 6q. Two independent genome-wide linkage analysis studies suggested a 3 Mb locus on chromosome 6q and two unrelated Swedish families with a LOD >2 together seemed to share a haplotype in 6q14.1. We hypothesized that this region harbored a rare high-risk founder allele contributing to breast cancer in these two families. Sequencing of DNA and RNA from the two families did not detect any pathogenic mutations. Finally, 29 SNPs in the region were analyzed in 44,214 cases and 43,532 controls from BCAC, and the original haplotypes in the two families were suggested as low-risk alleles for European and Swedish women specifically. There was also some support for one additional independent moderate-risk allele in Swedish familial samples. The results were consistent with our previous findings in familial breast cancer and supported a breast cancer susceptibility locus at 6q14.1 around the PHIP gene.