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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00005387naa a2200817 4500
001oai:DiVA.org:umu-111131
003SwePub
008151106s2015 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:132193794
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-1111312 URI
024a https://doi.org/10.1002/ijc.294462 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1321937942 URI
040 a (SwePub)umud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Barrdahl, Myrto4 aut
2451 0a Association of breast cancer risk loci with breast cancer survival
264 c 2015-08-14
264 1b Wiley-Blackwell,c 2015
338 a print2 rdacarrier
520 a The survival of breast cancer patients is largely influenced by tumor characteristics, such as TNM stage, tumor grade and hormone receptor status. However, there is growing evidence that inherited genetic variation might affect the disease prognosis and response to treatment. Several lines of evidence suggest that alleles influencing breast cancer risk might also be associated with breast cancer survival. We examined the associations between 35 breast cancer susceptibility loci and the disease over-all survival (OS) in 10,255 breast cancer patients from the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3) of which 1,379 died, including 754 of breast cancer. We also conducted a meta-analysis of almost 35,000 patients and 5,000 deaths, combining results from BPC3 and the Breast Cancer Association Consortium (BCAC) and performed in silico analyses of SNPs with significant associations. In BPC3, the C allele of LSP1-rs3817198 was significantly associated with improved OS (HRper-allele=0.70; 95% CI: 0.58-0.85; ptrend=2.84 x 10-4; HRheterozygotes=0.71; 95% CI: 0.55-0.92; HRhomozygotes=0.48; 95% CI: 0.31-0.76; p2DF=1.45 x 10-3). In silico, the C allele of LSP1-rs3817198 was predicted to increase expression of the tumor suppressor cyclin-dependent kinase inhibitor 1C (CDKN1C). In the meta-analysis, TNRC9-rs3803662 was significantly associated with increased death hazard (HRMETA =1.09; 95% CI: 1.04-1.15; ptrend=6.6 x 10-4; HRheterozygotes=0.96 95% CI: 0.90-1.03; HRhomozygotes=1.21; 95% CI: 1.09-1.35; p2DF=1.25 x 10-4). In conclusion, we show that there is little overlap between the breast cancer risk single nucleotide polymorphisms (SNPs) identified so far and the SNPs associated with breast cancer prognosis, with the possible exceptions of LSP1-rs3817198 and TNRC9-rs3803662.What's new? Genetic factors are known to influence the risk of breast cancer, but inherited genetic variation may also affect disease prognosis and response to treatment. In this study, the we investigated whether single nucleotide polymorphisms (SNPs) that are known to be associated with breast cancer risk might also influence the survival of breast-cancer patients. While two of the investigated SNPs may influence survival, there was otherwise no indication that SNP alleles related to breast cancer risk also play a role in the survival of breast cancer patients.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
653 a breast cancer
653 a SNP
653 a survival
653 a BPC3
653 a meta-analysis
700a Canzian, Federico4 aut
700a Lindström, Sara4 aut
700a Shui, Irene4 aut
700a Black, Amanda4 aut
700a Hoover, Robert N4 aut
700a Ziegler, Regina G4 aut
700a Buring, Julie E4 aut
700a Chanock, Stephen J4 aut
700a Diver, W Ryan4 aut
700a Gapstur, Susan M4 aut
700a Gaudet, Mia M4 aut
700a Giles, Graham G4 aut
700a Haiman, Christopher4 aut
700a Henderson, Brian E4 aut
700a Hankinson, Susan4 aut
700a Hunter, David J4 aut
700a Joshi, Amit D4 aut
700a Kraft, Peter4 aut
700a Lee, I-Min4 aut
700a Le Marchand, Loic4 aut
700a Milne, Roger L4 aut
700a Southey, Melissa C4 aut
700a Willett, Walter4 aut
700a Gunter, Marc4 aut
700a Panico, Salvatore4 aut
700a Sund, Malinu Umeå universitet,Kirurgi4 aut0 (Swepub:umu)masu0021
700a Weiderpass, Elisabeteu Karolinska Institutet4 aut
700a Sánchez, María-José4 aut
700a Overvad, Kim4 aut
700a Dossus, Laure4 aut
700a Peeters, Petra H4 aut
700a Khaw, Kay-Tee4 aut
700a Trichopoulos, Dimitrios4 aut
700a Kaaks, Rudolf4 aut
700a Campa, Daniele4 aut
710a Umeå universitetb Kirurgi4 org
773t International Journal of Cancerd : Wiley-Blackwellg 137:12, s. 2837-2845q 137:12<2837-2845x 0020-7136x 1097-0215
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.29446
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-111131
8564 8u https://doi.org/10.1002/ijc.29446
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:132193794

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