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  • Stacey, Simon N (author)

Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.

  • Article/chapterEnglish2010

Publisher, publication year, extent ...

  • 2010-07-22
  • Public Library of Science,2010
  • electronicrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:umu-35468
  • https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-35468URI
  • https://doi.org/10.1371/journal.pgen.1001029DOI
  • https://lup.lub.lu.se/record/1677328URI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:121099683URI

Supplementary language notes

  • Language:English
  • Summary in:English

Part of subdatabase

Classification

  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • We used an approach that we term ancestry-shift refinement mapping to investigate an association, originally discovered in a GWAS of a Chinese population, between rs2046210[T] and breast cancer susceptibility. The locus is on 6q25.1 in proximity to the C6orf97 and estrogen receptor alpha (ESR1) genes. We identified a panel of SNPs that are correlated with rs2046210 in Chinese, but not necessarily so in other ancestral populations, and genotyped them in breast cancer case:control samples of Asian, European, and African origin, a total of 10,176 cases and 13,286 controls. We found that rs2046210[T] does not confer substantial risk of breast cancer in Europeans and Africans (OR = 1.04, P = 0.099, and OR = 0.98, P = 0.77, respectively). Rather, in those ancestries, an association signal arises from a group of less common SNPs typified by rs9397435. The rs9397435[G] allele was found to confer risk of breast cancer in European (OR = 1.15, P = 1.2 x 10(-3)), African (OR = 1.35, P = 0.014), and Asian (OR = 1.23, P = 2.9 x 10(-4)) population samples. Combined over all ancestries, the OR was 1.19 (P = 3.9 x 10(-7)), was without significant heterogeneity between ancestries (P(het) = 0.36) and the SNP fully accounted for the association signal in each ancestry. Haplotypes bearing rs9397435[G] are well tagged by rs2046210[T] only in Asians. The rs9397435[G] allele showed associations with both estrogen receptor positive and estrogen receptor negative breast cancer. Using early-draft data from the 1,000 Genomes project, we found that the risk allele of a novel SNP (rs77275268), which is closely correlated with rs9397435, disrupts a partially methylated CpG sequence within a known CTCF binding site. These studies demonstrate that shifting the analysis among ancestral populations can provide valuable resolution in association mapping.

Subject headings and genre

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  • Sulem, Patrick (author)
  • Zanon, Carlo (author)
  • Gudjonsson, Sigurjon A (author)
  • Thorleifsson, Gudmar (author)
  • Helgason, Agnar (author)
  • Jonasdottir, Aslaug (author)
  • Besenbacher, Soren (author)
  • Kostic, Jelena P (author)
  • Fackenthal, James D (author)
  • Huo, Dezheng (author)
  • Adebamowo, Clement (author)
  • Ogundiran, Temidayo (author)
  • Olson, Janet E (author)
  • Fredericksen, Zachary S (author)
  • Wang, Xianshu (author)
  • Look, Maxime P (author)
  • Sieuwerts, Anieta MKarolinska Institutet (author)
  • Martens, John W M (author)
  • Pajares, Isabel (author)
  • Garcia-Prats, Maria D (author)
  • Ramon-Cajal, Jose M (author)
  • de Juan, Ana (author)
  • Panadero, Angeles (author)
  • Ortega, Eugenia (author)
  • Hemminki, KariLund University,Lunds universitet,Allmänmedicin och klinisk epidemiologi,Forskargrupper vid Lunds universitet,Family Medicine and Clinical Epidemiology,Lund University Research Groups(Swepub:lu)med-khk (author)
  • Vermeulen, Sita H (author)
  • Asadzadeh, Fatemeh (author)
  • van Engelenburg, K C Anton (author)
  • Margolin, Sara (author)
  • Shen, Chen-Yang (author)
  • Wu, Pei-Ei (author)
  • Försti, AstaLund University,Lunds universitet,Allmänmedicin och klinisk epidemiologi,Forskargrupper vid Lunds universitet,Family Medicine and Clinical Epidemiology,Lund University Research Groups(Swepub:lu)med-asf (author)
  • Lenner, PerUmeå universitet,Onkologi(Swepub:umu)pele0005 (author)
  • Henriksson, RogerUmeå universitet,Onkologi(Swepub:umu)rohe0003 (author)
  • Johansson, RobertUmeå universitet,Onkologi(Swepub:umu)rojo0001 (author)
  • Enquist, KerstinUmeå universitet,Näringsforskning (author)
  • Hallmans, GöranUmeå universitet,Näringsforskning(Swepub:umu)goha0001 (author)
  • Jonsson, Thorvaldur (author)
  • Sigurdsson, Helgi (author)
  • Alexiusdottir, Kristin (author)
  • Gudmundsson, Julius (author)
  • Sigurdsson, Asgeir (author)
  • Frigge, Michael L (author)
  • Gudmundsson, Larus (author)
  • Kristjansson, Kristleifur (author)
  • Halldorsson, Bjarni V (author)
  • Styrkarsdottir, Unnur (author)
  • Gulcher, Jeffrey R (author)
  • Hemminki, Kari (author)
  • Lindblom, AnnikaKarolinska Institutet (author)
  • Kiemeney, Lambertus A (author)
  • Mayordomo, Jose I (author)
  • Foekens, John A (author)
  • Couch, Fergus J (author)
  • Olopade, Olufunmilayo I (author)
  • Gudbjartsson, Daniel F (author)
  • Thorsteinsdottir, Unnur (author)
  • Rafnar, Thorunn (author)
  • Johannsson, Oskar T (author)
  • Stefansson, Kari (author)
  • Karolinska InstitutetAllmänmedicin och klinisk epidemiologi (creator_code:org_t)

Related titles

  • In:PLoS genetics: Public Library of Science6:7, s. e1001029-1553-7404

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