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Sökning: (WFRF:(Licaj Idlir)) > Polymorphisms of H....

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00005092naa a2200925 4500
001oai:DiVA.org:umu-76659
003SwePub
008130709s2014 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-766592 URI
024a https://doi.org/10.1002/ijc.283572 DOI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Companioni, Osmel4 aut
2451 0a Polymorphisms of H. pylori signaling pathway genes and gastric cancer risk in the European EPIC-eurgast cohort
264 c 2013-08-13
264 1b Wiley-Blackwell,c 2014
338 a print2 rdacarrier
500 a Article first published online: 13 Aug 2013
520 a Helicobacter pylori is a recognized causal factor of noncardia gastric cancer (GC). Lipopolysaccaride and peptidoglycan of this bacterium are recognized by CD14, TLR4 and NOD2 human proteins, while NFKB1 activates the transcription of pro-inflammatory cytokines to elicit an immune response. SNPs in these genes have been associated with GC in different populations. We genotyped 30 SNPs of these genes, in 365 gastric adenocarcinomas and 1284 matched controls from the EPIC cohort. The association with GC and its histological and anatomical subtypes was analyzed by logistic regression and corrected for multiple comparisons. Using a log-additive model we found a significant association between SNPs in CD14, NOD2 and TLR4 with GC risk. However, after applying the multiple comparisons tests only the NOD2 region remained significant (p=0.009). Analysis according to anatomical subtypes revealed NOD2 and NFKB1 SNPs associated with noncardia GC and CD14 SNPs associated with cardia GC, while analysis according to histological subtypes showed that CD14 was associated with intestinal but not diffuse GC. The multiple comparisons tests confirmed the association of NOD2 with noncardia GC (p=0.0003) and CD14 with cardia GC (p=0.01). Haplotype analysis was in agreement with single SNP results for NOD2 and CD14 genes. From these results we conclude that genetic variation in NOD2 associates with noncardia GC while variation in CD14 is associated with cardia GC.
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
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Kirurgi0 (SwePub)302122 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Surgery0 (SwePub)302122 hsv//eng
653 a gastric cancer
653 a genetic susceptibility
653 a Helicobacter pylori
653 a NOD2
653 a CD14
700a Bonet, Catalina4 aut
700a Muñoz, Xavier4 aut
700a Weiderpass, Elisabete4 aut
700a Panico, Salvatore4 aut
700a Tumino, Rosario4 aut
700a Palli, Domenico4 aut
700a Agnoli, Claudia4 aut
700a Vineis, Paolo4 aut
700a Boutron-Ruault, Marie-Christine4 aut
700a Racine, Antoine4 aut
700a Clavel-Chapelon, Françoise4 aut
700a Travis, Ruth C4 aut
700a Khaw, Kay-Tee4 aut
700a Riboli, Elio4 aut
700a Murphy, Neil4 aut
700a Vergnaud, Anne-Claire4 aut
700a Trichopoulou, Antonia4 aut
700a Benetou, Vassiliki4 aut
700a Trichopoulos, Dimitrios4 aut
700a Lund, Eiliv4 aut
700a Johansen, Dorthe4 aut
700a Lindkvist, Björn4 aut
700a Johansson, Mattiasu Umeå universitet,Enheten för biobanksforskning,International Agency for Research on Cancer (IARC-WHO), Lyon, France4 aut0 (Swepub:umu)masmas97
700a Sund, Malin,d 1972-u Umeå universitet,Kirurgi4 aut0 (Swepub:umu)masu0021
700a Ardanaz, Eva4 aut
700a Sánchez-Cantalejo, Emilio4 aut
700a Huerta, Jose M4 aut
700a Dorronsoro, Miren4 aut
700a Quirós, José Ramón4 aut
700a Tjonneland, Anne4 aut
700a Mortensen, Lotte Maxild4 aut
700a Overvad, Kim4 aut
700a Chang-Claude, Jenny4 aut
700a Rizzato, Cosmeri4 aut
700a Boeing, Heiner4 aut
700a de Mesquita, H Bas Bueno4 aut
700a Siersema, Peter4 aut
700a Peeters, Petra Hm4 aut
700a Numans, Mattijs E4 aut
700a Carneiro, Fatima4 aut
700a Licaj, Idlir4 aut
700a Freisling, Heinz4 aut
700a Sala, Núria4 aut
700a González, Carlos A4 aut
710a Umeå universitetb Enheten för biobanksforskning4 org
773t International Journal of Cancerd : Wiley-Blackwellg 134:1, s. 92-101q 134:1<92-101x 0020-7136x 1097-0215
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.28357
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-76659
8564 8u https://doi.org/10.1002/ijc.28357

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