Publication:
Fas and Fas Ligand Expression and Relationship with Clinicopathologic Parameters in Pancreas Cancer

dc.authorscopusid6506410014
dc.authorscopusid57197115377
dc.authorscopusid6603942124
dc.authorscopusid6602587152
dc.contributor.authorGönüllü, G.
dc.contributor.authorÖztürk, H.
dc.contributor.authorEvrensel, T.
dc.contributor.authorManavoǧlu, O.
dc.date.accessioned2020-06-21T15:06:32Z
dc.date.available2020-06-21T15:06:32Z
dc.date.issued2009
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Gönüllü] Güzin, Department of Medical Oncology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Öztürk] Hülya,; [Evrensel] Türkkan, Bursa Uludağ Üniversitesi, Bursa, Bursa, Turkey; [Manavoǧlu] Osman, Bursa Uludağ Üniversitesi, Bursa, Bursa, Turkeyen_US
dc.description.abstractObjective: Fas (GD95/APO-1) and Fas Ligand (FasL) are important in the process of apoptosis in the immune system. Hereby, we aimed to examine the expression of Fas/FasL in pancreatic adenocarcinoma and chronic pancreatic tissue and its relation with clinicopathological characteristics using immunohistochemical studies. Material and Methods: Pancreatic adenocarcinoma (n= 35) and chronic pancreatitis cases (n= 25) underwent assessment for Fas and FasL expression using immunohistochemistry. Results: The cancer group consisted of 24 female and 11 male patients, while the chronic pancreatitis group included 21 female and 4 male patients. All patients had been diagnosed with adenocarcinoma. According to the International Union Against Cancer (UICC) staging, 19 patients were classified as stage III (unresectable) and 16 patients had stage IV disease. All patients classified as stage III were revealed to have unresectable tumors intraoperatively. The loss of Fas expression was higher in pancreatic adenocarcinoma than in chronic pancreatitis (57.1% vs. 292%, p= 0.034). FasL over-expression was higher in pancreatic adenocarcinoma than in chronic pancreatitis (57.1% vs. 26.1%, p= 0.031). Cytoplasmic staining of Fas (77.1% vs. 22.9%, p= 0.016) and FasL (61.1% vs. 38.9%, p= 0.002) was higher than membranous staining. According to stages, loss of Fas expression was greater in stage IV when compared with stage III (73.9% vs. 25%, p= 0.01). There was no significant relationship between Fas and the stage of cancer (p> 0.05). Furthermore, there was no correlation between Fas/FasL staining and age and sex (p> 0.05). Conclusion: In pancreatic adenocarcinoma, loss of Fas expression and Fas L over-expression were statistically significant. Copyright © 2009 by Türkiye Klinikleri.en_US
dc.identifier.endpage588en_US
dc.identifier.issn1300-0292
dc.identifier.issue3en_US
dc.identifier.scopus2-s2.0-69949161204
dc.identifier.scopusqualityQ4
dc.identifier.startpage584en_US
dc.identifier.volume29en_US
dc.identifier.wosWOS:000268007400002
dc.language.isoenen_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.journalTurkiye Klinikleri Tip Bilimleri Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectFas Ligand Proteinen_US
dc.subjectPancreatic Neoplasmsen_US
dc.titleFas and Fas Ligand Expression and Relationship with Clinicopathologic Parameters in Pancreas Canceren_US
dc.typeArticleen_US
dspace.entity.typePublication

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