Fibulin1 and mesothelin expressions in pancreas ductal adenocarcinoma

dc.contributor.authorAksoy, Asude
dc.contributor.authorArtas, Gokhan
dc.contributor.authorKuloglu, Tuncay
dc.contributor.authorKoc, Mustafa
dc.date.accessioned2026-08-12T17:21:01Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractOBJECTIVE: The balance between malignant tumor cells and the connective tissue surrounding them determines the ag-gressiveness of the tumor. We aimed to understand the effects of mesothelin (MSLN) and fibulin1 (FBLN1) expressions on survival in pancreas ductal adenocarcinoma (PDCA), and also whether these proteins have prognostic value for PDCA.METHODS: Of 80 patients in total, 40 who underwent the Whipple procedure for diagnosed PDCA between 2009 and 2016, and 40 patients with diagnosed pancreatitis as the control group, were included in the present study. Immunohistochemically, MSLN, and FBLN1 expressions were evaluated retrospectively. We assessed the relationship between the degree of MSLN, FBLN1 expression, clinical-pathological features, and survival rates in PDCA cases.RESULTS: The median follow-up duration was 11.4 (3-41) months. All of the patients for MSLN and FBLN1 were immune reactive. We detected a significant difference in MSLN expression between patients with PDCA and control groups, but not in FBLN1 expression. MSLN, FBLN1 expressions were categorized as lower-higher (L/H) groupings. There was no difference in the median overall survival (OS) of patients in the MSLN groups. The L-FBLN1 group had a median OS of 18 months (95% CI: 9.51-26.48) versus 14 months (95% CI: 13.021-14.97) in the H-FBLN1 group (interconnective tissue) (p=0.035). According to Kaplan-Meier analysis, L-FBLN1 expression in the tumor microenvironment was associated with longer survival in PDCA. The FBLN1 expression in the tumor microenvironment was shown to be significantly inversely related to OS (p=0.05).CONCLUSION: The FBLN1 expression, which is in the tumor microenvironment of PDCA, may serve as a prognostic biomarker.
dc.identifier.doi10.14744/nci.2022.49260
dc.identifier.endpage321
dc.identifier.issn2148-4902
dc.identifier.issn2536-4553
dc.identifier.issue3
dc.identifier.orcid0000-0001-9874-3838
dc.identifier.pmid37435286
dc.identifier.scopus2-s2.0-85164718117
dc.identifier.scopusqualityQ3
dc.identifier.startpage314
dc.identifier.trdizinid1189856
dc.identifier.urihttps://doi.org/10.14744/nci.2022.49260
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1189856
dc.identifier.urihttps://hdl.handle.net/11508/53770
dc.identifier.volume10
dc.identifier.wosWOS:001041293500005
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherKare Publ
dc.relation.ispartofNorthern Clinics of Istanbul
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectFibulin1
dc.subjectmesothelin
dc.subjectpancreas ductal adenocarcinoma
dc.subjectprognosis
dc.subjecttumor microenvironment
dc.titleFibulin1 and mesothelin expressions in pancreas ductal adenocarcinoma
dc.typeArticle

Dosyalar