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FältnamnIndikatorerMetadata
00006863naa a2201105 4500
001oai:gup.ub.gu.se/210477
003SwePub
008240528s2015 | |||||||||||000 ||eng|
009oai:lup.lub.lu.se:0859d1ef-21ba-4256-b8ce-8fd28d02f727
009oai:DiVA.org:umu-95217
009oai:prod.swepub.kib.ki.se:130277440
024a https://gup.ub.gu.se/publication/2104772 URI
024a https://doi.org/10.1002/ijc.290342 DOI
024a https://lup.lub.lu.se/record/49506712 URI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-952172 URI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1302774402 URI
040 a (SwePub)gud (SwePub)lud (SwePub)umud (SwePub)ki
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Duell, E. J.4 aut
2451 0a Variation at ABO histo-blood group and FUT loci and diffuse and intestinal gastric cancer risk in a European population
264 c 2014-07-01
264 1b Wiley,c 2015
520 a ABO blood serotype A is known to be associated with risk of gastric cancer (GC), but little is known how ABO alleles and the fucosyltransferase (FUT) enzymes and genes which are involved in Lewis antigen formation [and in Helicobacter pylori (H. pylori) binding and pathogenicity] may be related to GC risk in a European population. The authors conducted an investigation of 32 variants at ABO and FUT1-7 loci and GC risk in a case-control study of 365 cases and 1,284 controls nested within the EPIC cohort (the EPIC-Eurgast study). Four variants (including rs505922) in ABO, and allelic blood group A (AO+AA, odds ratio=1.84, 95%CI=1.20-2.80) were associated with diffuse-type GC; however, conditional models with other ABO variants indicated that the associations were largely due to allelic blood group A. One variant in FUT5 was also associated with diffuse-type GC, and four variants (and haplotypes) in FUT2 (Se), FUT3 (Le) and FUT6 with intestinal-type GC. Further, one variant in ABO, two in FUT3 and two in FUT6 were associated with H. pylori infection status in controls, and two of these (in FUT3 and FUT6) were weakly associated with intestinal-type GC risk. None of the individual variants surpassed a Bonferroni corrected p-value cutoff of 0.0016; however, after a gene-based permutation test, two loci [FUT3(Le)/FUT5/FUT6 and FUT2(Se)] were significantly associated with diffuse- and intestinal-type GC, respectively. Replication and functional studies are therefore recommended to clarify the role of ABO and FUT alleles in H. pylori infection and subtype-specific gastric carcinogenesis. What's New? Blood type A indicates a higher risk of gastric cancer, but why? This study examined the relationship between blood group genes and cancer. The authors investigated 32 variants among not only the ABO alleles, but also including the genes involved in producing the Lewis blood group antigens. They confirmed blood group A as a risk factor for diffuse-type gastric cancer, and also detected an association between certain Lewis antigen alleles and intestinal-type gastric cancer. Interestingly, these alleles also popped up among controls who harbored H. pylori infection. These associations certainly warrant further investigation into their role in gastric cancer.
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 gastric cancer
653 a blood group
653 a ABO
653 a FUT
653 a genetic susceptibility
653 a HELICOBACTER-PYLORI INFECTION
653 a ANTIGEN-BINDING ADHESIN
653 a GENOME-WIDE
653 a ASSOCIATION
653 a PANCREATIC-CANCER
653 a COHORT CONSORTIUM
653 a LEWIS ANTIGENS
653 a GROUP
653 a ALLELES
653 a EXPRESSION
653 a VITAMIN-B-12
653 a METAANALYSIS
653 a Oncology
700a Bonet, C.4 aut
700a Munoz, X.4 aut
700a Lujan-Barroso, L.4 aut
700a Weiderpass, E.u Karolinska Institutet4 aut
700a Boutron-Ruault, M. C.4 aut
700a Racine, A.4 aut
700a Severi, G.4 aut
700a Canzian, F.4 aut
700a Rizzato, C.4 aut
700a Boeing, H.4 aut
700a Overvad, K.4 aut
700a Tjonneland, A.4 aut
700a Arguelles, M.4 aut
700a Sanchez-Cantalejo, E.4 aut
700a Chamosa, S.4 aut
700a Huerta, J. M.u Umeå universitet,Enheten för biobanksforskning4 aut
700a Barricarte, A.4 aut
700a Khaw, K. T.4 aut
700a Wareham, N.4 aut
700a Travis, R. C.4 aut
700a Trichopoulou, A.4 aut
700a Trichopoulos, D.4 aut
700a Yiannakouris, N.4 aut
700a Palli, D.4 aut
700a Agnoli, C.4 aut
700a Tumino, R.4 aut
700a Naccarati, A.4 aut
700a Panico, S.4 aut
700a Bueno-de-Mesquita, H. B.4 aut
700a Siersema, P. D.4 aut
700a Peeters, P. H. M.4 aut
700a Ohlsson, Bodilu Lund University,Lunds universitet,Internmedicin - epidemiologi,Forskargrupper vid Lunds universitet,Internal Medicine - Epidemiology,Lund University Research Groups4 aut0 (Swepub:lu)kir-boh
700a Lindkvist, Björnu Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine4 aut0 (Swepub:gu)xlibjo
700a Johansson, Ingegerdu Umeå universitet,Enheten för biobanksforskning,Näringsforskning,Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden4 aut0 (Swepub:umu)injo0003
700a Ye, W. M.u Karolinska Institutet,Umeå universitet,Enheten för biobanksforskning,Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden4 aut
700a Johansson, M.4 aut
700a Fenger, C.4 aut
700a Riboli, E.4 aut
700a Sala, N.4 aut
700a Gonzalez, C. A.4 aut
710a Karolinska Institutetb Enheten för biobanksforskning4 org
773t International Journal of Cancerd : Wileyg 136:4, s. 880-893q 136:4<880-893x 0020-7136x 1097-0215
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.29034
856u http://dx.doi.org/10.1002/ijc.29034y FULLTEXT
8564 8u https://gup.ub.gu.se/publication/210477
8564 8u https://doi.org/10.1002/ijc.29034
8564 8u https://lup.lub.lu.se/record/4950671
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-95217
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:130277440

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