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The expression of syndecan-1 is related to the risk of endometrial hyperplasia progressing to endometrial carcinoma.

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dc.contributor.authorKim, H-
dc.contributor.authorChoi, DS-
dc.contributor.authorChang, SJ-
dc.contributor.authorHan, JH-
dc.contributor.authorMin, CK-
dc.contributor.authorChang, KH-
dc.contributor.authorRyu, HS-
dc.date.accessioned2011-06-07T05:18:47Z-
dc.date.available2011-06-07T05:18:47Z-
dc.date.issued2010-
dc.identifier.issn2005-0380-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/2820-
dc.description.abstractOBJECTIVE: Aberrant expression of the cell surface proteoglycan, syndecan-1, is found in many malignancies. The current study describes the immunohistochemical study of syndecan-1 expression in normal, hyperplastic, and malignant endometrial tissues for evaluation of application as a parameter of cancer progression in patients with endometrial hyperplasia.

METHODS: Immunohistochemical staining of syndecan-1 was performed in 101 formalin fixed, paraffin embedded sections of normal, hyperplastic, and malignant endometrial tissues. We analyzed specimens from patients with normal endometrium (NE, N=10) as controls, and those of simple hyperplasia (SH, N=20), complex hyperplasia without atypia (CH, N=20), atypical hyperplasia (AH, N=20), and endometrial cancer (EC, N=31).

RESULTS: The mean rank of expression scores based on the frequency of syndecan-1 staining were 31.6, 20.5, 52.9, 72.1, and 62.1 for NE, SH, CH, AH and EC, respectively (p<0.001). Syndecan-1 expression was significantly greater in CH (p<0.001) or AH (p<0.001) than in SH, and significantly greater in AH compared to CH (p=0.028). Syndecan-1 is more frequently expressed in CH (p=0.042), AH (p<0.001), or EC (p=0.002) than in NE. Syndecan-1 expression did not differ significantly between NE and SH (p=0.248).

CONCLUSION: Syndecan-1 expression appears to be useful as a predictive indicator in endometrial hyperplasia.
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dc.language.isoen-
dc.titleThe expression of syndecan-1 is related to the risk of endometrial hyperplasia progressing to endometrial carcinoma.-
dc.typeArticle-
dc.identifier.pmid20379448-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2849949/-
dc.contributor.affiliatedAuthor장, 석준-
dc.contributor.affiliatedAuthor한, 재호-
dc.contributor.affiliatedAuthor장, 기홍-
dc.contributor.affiliatedAuthor유, 희석-
dc.type.localJournal Papers-
dc.identifier.doi10.3802/jgo.2010.21.1.50-
dc.citation.titleJournal of gynecologic oncology-
dc.citation.volume21-
dc.citation.number1-
dc.citation.date2010-
dc.citation.startPage50-
dc.citation.endPage55-
dc.identifier.bibliographicCitationJournal of gynecologic oncology, 21(1). : 50-55, 2010-
dc.identifier.eissn2005-0399-
dc.relation.journalidJ020050380-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Obstetrics & Gynecology
Journal Papers > School of Medicine / Graduate School of Medicine > Pathology
Journal Papers > School of Medicine / Graduate School of Medicine > Medical Humanities & Social Medicine
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