Publication:
T-cadherin, e-cadherin, pr-a, and er-alpha levels in deep infiltrating endometriosis

dc.contributor.coauthorBıyık, İsmail
dc.contributor.coauthorŞimsek, Sercan
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberNo
dc.contributor.kuauthorKalkan, Üzeyir
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:49:07Z
dc.date.issued2022
dc.description.abstractThe goal of this study was to compare the T-cadherin, E-cadherin, progesterone receptor (PR), and estrogen receptor (ER) staining levels of deep infiltrating endometriosis (DIE) tissue, ovarian endometriomas and normal endometrial tissues in the same individuals. The tissue sections of both DIE nodule(s) and endometrioma(s) of 15 cases were examined. As a control group, normal endometrial tissue sections of 23 cases were examined. T-cadherin, E-cadherin, ER-alpha, and PR-A staining levels of DIE, endometrioma tissues, and endometrial tissues were compared immunohistochemically. H-score was calculated to compare the expression of T-cadherin, E-cadherin, ER-alpha, and PR-A in immunohistochemical staining based on the percentage of cells stained at each intensity level. T-cadherin, E-cadherin, ER, and PR H-score were lowest in DIE tissue and highest in endometrial tissue (P<0.0001, <0.0001, <0.0001, and <0.0001, respectively). In correlation analysis, a positive correlation was found between T-cadherin, E-cadherin, PR, and ER H-score (P<0.0001 for each). T-cadherin, E-cadherin, ER, and PR H-score were lowest in DIE tissue and highest in endometrium tissue. We think that examination of DIE tissue and endometrioma tissue from the same individual excludes the possibility of an effect due to different genetic and environmental factors from different individuals. With the help of this exclusion we showed that DIE and endometrioma have different biological properties.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1097/PGP.0000000000000860
dc.identifier.eissn1538-7151
dc.identifier.embargoN/A
dc.identifier.endpage599
dc.identifier.issn0277-1691
dc.identifier.issue6
dc.identifier.pubmed35149616
dc.identifier.scopus2-s2.0-85125709297
dc.identifier.startpage593
dc.identifier.urihttps://doi.org/10.1097/PGP.0000000000000860
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14314
dc.identifier.volume41
dc.identifier.wos000874079300008
dc.keywordsT-cadherin
dc.keywordsE-cadherin
dc.keywordsProgesterone receptor
dc.keywordsEstrogen receptor
dc.keywordsEndometriosis
dc.keywordsDIE
dc.keywordsEndometrioma
dc.language.isoeng
dc.publisherLippincott Williams and Wilkins
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofInternational Journal of Gynecological Pathology
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectObstetrics and gynecology
dc.subjectPathology
dc.titleT-cadherin, e-cadherin, pr-a, and er-alpha levels in deep infiltrating endometriosis
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKalkan, Üzeyir
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relation.isGoalOfPublication.latestForDiscoverya9786601-9431-4553-9a46-013bb366fb87
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