Ghrelin expression of endometrium hyperplasia and endometrioid carcinoma

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Background. Endometrium carcinoma ranks fourth among female carcinomas. Therefore, early diagnosis of endometrium pre-malignant lesions is emphasised, and attempts are made to identify the risk factors. Since hyperplasias, particularly those with atypia, are held responsible for the development of the most common endometrium carcinomas, it is important to definitely distinguish between well-differentiated carcinomas and hyperplasia with atypia. In the present study, we aimed to explore whether ghrelin expression had a role in distinguishing between benign, pre-malignant and malignant lesions of endometrium. Methods. Tissue ghrelin expressions of a total of 60 cases, who were diagnosed in the Pathology Department Laboratory of Fiirat University Medical School, and of whom 10 were in the proliferation phase, 10 had simple hyperplasia without atypia, 10 had simple hyperplasia with atypia, 10 had complex hyperplasia without atypia, 10 had complex hyperplasia with atypia and 10 had endometrioid carcinoma cases, were examined using immunohistochemical method. Additionally, tissue samples were homogenised to analyse tissue ghrelin levels in the supernatants according to RIA method. Samples from the parotid glands were used as positive control for ghrelin. Cells that exhibited cytoplasmic staining with ghrelin antibody were evaluated as positive. Results. Immunohistochemical examination showed that ghrelin expression increased markedly in the proliferation phase, relative to hyperplasias and carcinoma. These results were parallel to ghrelin levels in tissue supernatants. Immunohistochemical and RIA analysis results indicate that ghrelin expression either markedly decreases or is entirely depleted in endometrial carcinomas. Conclusions. Therefore, we think that ghrelin expression can be useful in differentiating not only endometrium carcinomas from benign lesions but also complex hyperplasias with atypia, which pose diagnostic difficulties. © 2010 Informa UK, Ltd.

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AlanDeğerDil
dc.contributor.authorDagli, Adile F.
dc.contributor.authorAydin, Suleyman
dc.contributor.authorKocdor, Hilal
dc.contributor.authorGurates, Bilgin
dc.contributor.authorSahin, Ibrahim
dc.contributor.authorCatak, Zekiye
dc.contributor.authorOzercan, Mehmet R.
dc.contributor.authorOzercan, Ibrahim. H.
dc.date.accessioned2026-10-18T20:30:45.771753019Z
dc.date.available2026-10-18T20:30:45.771753019Z
dc.date.issued2011
dc.description.abstractBackground. Endometrium carcinoma ranks fourth among female carcinomas. Therefore, early diagnosis of endometrium pre-malignant lesions is emphasised, and attempts are made to identify the risk factors. Since hyperplasias, particularly those with atypia, are held responsible for the development of the most common endometrium carcinomas, it is important to definitely distinguish between well-differentiated carcinomas and hyperplasia with atypia. In the present study, we aimed to explore whether ghrelin expression had a role in distinguishing between benign, pre-malignant and malignant lesions of endometrium. Methods. Tissue ghrelin expressions of a total of 60 cases, who were diagnosed in the Pathology Department Laboratory of Fiirat University Medical School, and of whom 10 were in the proliferation phase, 10 had simple hyperplasia without atypia, 10 had simple hyperplasia with atypia, 10 had complex hyperplasia without atypia, 10 had complex hyperplasia with atypia and 10 had endometrioid carcinoma cases, were examined using immunohistochemical method. Additionally, tissue samples were homogenised to analyse tissue ghrelin levels in the supernatants according to RIA method. Samples from the parotid glands were used as positive control for ghrelin. Cells that exhibited cytoplasmic staining with ghrelin antibody were evaluated as positive. Results. Immunohistochemical examination showed that ghrelin expression increased markedly in the proliferation phase, relative to hyperplasias and carcinoma. These results were parallel to ghrelin levels in tissue supernatants. Immunohistochemical and RIA analysis results indicate that ghrelin expression either markedly decreases or is entirely depleted in endometrial carcinomas. Conclusions. Therefore, we think that ghrelin expression can be useful in differentiating not only endometrium carcinomas from benign lesions but also complex hyperplasias with atypia, which pose diagnostic difficulties. © 2010 Informa UK, Ltd.
dc.identifier.doi10.3109/09513590.2010.488772
dc.identifier.eissn1473-0766
dc.identifier.endpage204
dc.identifier.issn1473-0766
dc.identifier.issue3
dc.identifier.pmid20712427
dc.identifier.scopus2-s2.0-78650198282
dc.identifier.startpage199
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15914
dc.identifier.volume27
dc.identifier.wosWOS:000286993200012
dc.language.isoen
dc.publisherTAYLOR & FRANCIS LTD
dc.relation.ispartofGynecological Endocrinology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcomplex hyperplasia
dc.subjectendometrioid carcinoma
dc.subjectGhrelin
dc.subjectproliferation phase
dc.subjectsimple hyperplasia
dc.subjectEndometrial Hyperplasia
dc.subjectEndometrial Neoplasms
dc.subjectFemale
dc.subjectHumans
dc.subjectImmunohistochemistry
dc.subjectRadioimmunoassay
dc.subjectRetrospective Studies
dc.subjectTumor Markers, Biological
dc.subjectarticle
dc.subjectbenign tumor
dc.subjectcontrolled study
dc.subjectcytoplasm
dc.subjectendometrium
dc.subjectendometrium hyperplasia
dc.subjecthuman
dc.subjecthuman tissue
dc.subjecthyperplasia
dc.subjectmalignant transformation
dc.subjectparotid gland
dc.subjectprecancer
dc.subjectpriority journal
dc.subjectprotein expression
dc.subjectsupernatant
dc.subjecttissue
dc.subjecttumor growth
dc.titleGhrelin expression of endometrium hyperplasia and endometrioid carcinoma
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus7
rdl.citation.wos8
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)