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(WFRF:(Haiman Christopher)) lar1:(umu)
 

Sökning: (WFRF:(Haiman Christopher)) lar1:(umu) > Post-G WAS gene-env...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004505naa a2200769 4500
001oai:DiVA.org:umu-96615
003SwePub
008141124s2014 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-966152 URI
024a https://doi.org/10.1093/hmg/ddu2232 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Barrdahl, Myrto4 aut
2451 0a Post-G WAS gene-environment interplay in breast cancer :b results from the Breast and Prostate Cancer Cohort Consortium and a meta-analysis on 79 000 women
264 c 2014-05-08
264 1b Oxford University Press (OUP),c 2014
338 a print2 rdacarrier
520 a We studied the interplay between 39 breast cancer (BC) risk SNPs and established BC risk (body mass index, height, age at menarche, parity, age at menopause, smoking, alcohol and family history of BC) and prognostic factors (TNM stage, tumor grade, tumor size, age at diagnosis, estrogen receptor status and progesterone receptor status) as joint determinants of BC risk. We used a nested case-control design within the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium (BPC3), with 16 285 BC cases and 19 376 controls. We performed stratified analyses for both the risk and prognostic factors, testing for heterogeneity for the risk factors, and case-case comparisons for differential associations of polymorphisms by subgroups of the prognostic factors. We analyzed multiplicative interactions between the SNPs and the risk factors. Finally, we also performed a meta-analysis of the interaction ORs from BPC3 and the Breast Cancer Association Consortium. After correction for multiple testing, no significant interaction between the SNPs and the established risk factors in the BPC3 study was found. The meta-analysis showed a suggestive interaction between smoking status and SLC4A7-rs4973768 (P-interaction = 8.84 x 10(-4)) which, although not significant after considering multiple comparison, has a plausible biological explanation. In conclusion, in this study of up to almost 79 000 women we can conclusively exclude any novel major interactions between genome-wide association studies hits and the epidemiologic risk factors taken into consideration, but we propose a suggestive interaction between smoking status and SLC4A7-rs4973768 that if further replicated could help our understanding in the etiology of BC.
700a Canzian, Federico4 aut
700a Joshi, Amit D.4 aut
700a Travis, Ruth C.4 aut
700a Chang-Claude, Jenny4 aut
700a Auer, Paul L.4 aut
700a Gapstur, Susan M.4 aut
700a Gaudet, Mia4 aut
700a Diver, W. Ryan4 aut
700a Henderson, Brian E.4 aut
700a Haiman, Christopher A.4 aut
700a Schumacher, Fredrick R.4 aut
700a Le Marchand, Loic4 aut
700a Berg, Christine D.4 aut
700a Chanock, Stephen J.4 aut
700a Hoover, Robert N.4 aut
700a Rudolph, Anja4 aut
700a Ziegler, Regina G.4 aut
700a Giles, Graham G.4 aut
700a Baglietto, Laura4 aut
700a Severi, Gianluca4 aut
700a Hankinson, Susan E.4 aut
700a Lindstroem, Sara4 aut
700a Willet, Walter4 aut
700a Hunter, David J.4 aut
700a Buring, Julie E.4 aut
700a Lee, I-Min4 aut
700a Zhang, Shumin4 aut
700a Dossus, Laure4 aut
700a Cox, David G.4 aut
700a Khaw, Kay-Tee4 aut
700a Lund, Eiliv4 aut
700a Naccarati, Alessio4 aut
700a Peeters, Petra H.4 aut
700a Ramon Quiros, J.4 aut
700a Riboli, Elio4 aut
700a Sund, Malin,d 1972-u Umeå universitet,Kirurgi4 aut0 (Swepub:umu)masu0021
700a Trichopoulos, Dimitrios4 aut
700a Prentice, Ross L.4 aut
700a Kraft, Peter4 aut
700a Kaaks, Rudolf4 aut
700a Campa, Daniele4 aut
710a Umeå universitetb Kirurgi4 org
773t Human Molecular Geneticsd : Oxford University Press (OUP)g 23:19, s. 5260-5270q 23:19<5260-5270x 0964-6906x 1460-2083
856u https://academic.oup.com/hmg/article-pdf/23/19/5260/17260677/ddu223.pdf
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-96615
8564 8u https://doi.org/10.1093/hmg/ddu223

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