Genetic polymorphisms of interleukin 1 beta gene and sporadic pancreatic neuroendocrine tumors susceptibility
dc.contributor.author | Karakaxas, Dimitrios | |
dc.contributor.author | Sioziou, Anna | |
dc.contributor.author | Aravantinos, Gerasimos | |
dc.contributor.author | Coker, Ahmet | |
dc.contributor.author | Papanikolaou, Ioannis S. | |
dc.contributor.author | Liakakos, Theodoros | |
dc.contributor.author | Dervenis, Christos | |
dc.contributor.author | Gazouli, Maria | |
dc.date.accessioned | 2019-10-27T23:09:27Z | |
dc.date.available | 2019-10-27T23:09:27Z | |
dc.date.issued | 2016 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | AIM: To evaluate the association between the inter-leukin 1 beta (IL-1 beta) polymorphisms and the pancreatic neuroendocrine tumor (pNET) development. METHODS: A case-control study was conducted analyzing IL-1 beta polymorphisms using germline DNA collected in a population-based case-control study of pancreatic cancer (51 pNET cases, 85 pancreatic ductal adenocarcinoma cases, 19 intraductal papillary mucinous neoplasm and 98 healthy controls). RESULTS: The distribution of genotypes for the -511 C/T polymorphism in the pNET patient groups showed significant difference compared to the control group. It is known that the carriers of the IL-1 beta -511T allele have increased concentrations of IL-1 beta. The -511 CT and TT high-expression genotypes were over-represented in pNET patients. CONCLUSION: The findings of this study suggested a possible role of IL-1 beta -511 C/T genotypes in the pathogenesis of pNETs since the presence of the IL-1 beta -511 CT and TT genotypes and the T allele was associated with an increased risk of pNET only. | en_US |
dc.description.sponsorship | Hellenic Society of Medical Oncology [5839/08-04-2015] | en_US |
dc.description.sponsorship | Supported by Hellenic Society of Medical Oncology, No. 5839/08-04-2015. | en_US |
dc.identifier.doi | 10.4251/wjgo.v8.i6.520 | en_US |
dc.identifier.endpage | 525 | en_US |
dc.identifier.issn | 1948-5204 | |
dc.identifier.issue | 6 | en_US |
dc.identifier.pmid | 27326321 | en_US |
dc.identifier.startpage | 520 | en_US |
dc.identifier.uri | https://doi.org/10.4251/wjgo.v8.i6.520 | |
dc.identifier.uri | https://hdl.handle.net/11454/52651 | |
dc.identifier.volume | 8 | en_US |
dc.identifier.wos | WOS:000408543000005 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Baishideng Publishing Group Inc | en_US |
dc.relation.ispartof | World Journal of Gastrointestinal Oncology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Interleukin 1 beta | en_US |
dc.subject | Neuroendocrine tumors | en_US |
dc.subject | Pancreas | en_US |
dc.title | Genetic polymorphisms of interleukin 1 beta gene and sporadic pancreatic neuroendocrine tumors susceptibility | en_US |
dc.type | Article | en_US |