Publication:
Immunohistochemical determination of hif, tsp-1, adamts1, and adamts8 expressions in the brains of alzheimer's disease patients: A preliminary autopsy study

dc.contributor.authorEren, Filiz
dc.contributor.authorEren, Bülent
dc.contributor.authorDemircan, Kadir
dc.contributor.authorAkyol, Sümeyya
dc.contributor.authorAynekin, Büşra
dc.contributor.buuauthorTÜRKMEN İNANIR, NURSEL
dc.contributor.buuauthorFedakar, Recep
dc.contributor.buuauthorFEDAKAR, RECEP
dc.contributor.buuauthorGürses, Murat Serdar
dc.contributor.buuauthorUral, Mustafa
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentAdli Tıp Ana Bilim Dalı
dc.contributor.researcheridJAC-4250-2023
dc.contributor.researcheridACP-5545-2022
dc.contributor.researcheridAAH-6287-2021
dc.date.accessioned2024-11-28T11:07:58Z
dc.date.available2024-11-28T11:07:58Z
dc.date.issued2016-03-01
dc.description.abstractObjective: Alzheimer's disease (AD) is a progressive neurodegenerative disease that mostly affects the elderly population. Recent studies performed in AD highlight the pathophysiological relevance of disintegrin and metalloproteinase with thrombospondin type 1-like motifs (ADAMTS) genes and their products, namely hypoxia inducible factor-1 (HIF-1) and thrombospondin-1 (TSP-1). Thus, the aim of this study was to describe and identify the distribution, characteristics, and any changes in the expression and immunoreactivity for HIF-1, TSP-1, and ADAMTS1 and 8 in AD brains.Materials and Methods: Nine patients who were autopsied in the Council of Forensic Medicine, Bursa Morgue Department in 2013, were selected. All patients were sent for autopsy to the Morgue Department within 8 h after death. At the autopsy, tissue samples of the organs were obtained for histopathological examination for determining the cause of death. Among these, two patients were clinically diagnosed with AD.Results: Immunohistochemical staining was performed, and the staining intensity/extensity was evaluated using a semi-quantitative scoring system. Median distribution (extensity) scores of the immunohistochemical staining were estimated as 2 for HIF-1, 0.67 for TSP-1, 3.11 for ADAMTS1, and 2.78 for ADAMTS8. Intensity scores were estimated as 1.22 for HIF-1, 0.56 for TSP-1, 3 for ADAMTS1, and 2.11 for ADAMTS8.Conclusion: Our study suggests that ADAMTS1 and ADAMTS8 expressions are not specific for AD. To understand and provide definitive data on all aspects of metalloproteinases, extracellular matrix proteins, and transcriptional factor effects to AD, further studies are needed, where other metalloproteinases and related molecules/enzymes should be studied.
dc.identifier.doi10.5152/etd.2016.0061
dc.identifier.endpage5
dc.identifier.issn2149-2247
dc.identifier.issue1
dc.identifier.startpage1
dc.identifier.urihttps://doi.org/10.5152/etd.2016.0061
dc.identifier.urihttps://hdl.handle.net/11452/48644
dc.identifier.volume38
dc.identifier.wos000372329600002
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherErciyes Univ Sch Medicine
dc.relation.journalErciyes Medical Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCerebral-artery occlusion
dc.subjectInducible factor-i
dc.subjectHypoxia
dc.subjectThrombospondin
dc.subjectMetalloproteinase
dc.subjectProteins
dc.subjectMotifs
dc.subjectRat
dc.subjectAlzheimer's disease
dc.subjectAdamts1
dc.subjectHif-1
dc.subjectAdamts8
dc.subjectTsp-1
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectMedicine, general & internal
dc.subjectGeneral & internal medicine
dc.titleImmunohistochemical determination of hif, tsp-1, adamts1, and adamts8 expressions in the brains of alzheimer's disease patients: A preliminary autopsy study
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Adli Tıp Ana Bilim Dalı
relation.isAuthorOfPublicationb47dba7f-e6a6-4844-a4de-3d51ee5a82c4
relation.isAuthorOfPublication64310c17-8b59-40c0-8b34-8de15da2a3da
relation.isAuthorOfPublication.latestForDiscoveryb47dba7f-e6a6-4844-a4de-3d51ee5a82c4

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