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dc.contributor.authorZagorianakou, N.en
dc.contributor.authorStefanou, D. G.en
dc.contributor.authorMakrydimas, G.en
dc.contributor.authorZagorianakou, P.en
dc.contributor.authorBriassoulis, E. Chen
dc.contributor.authorKaravasilis, V.en
dc.contributor.authorPavlidis, Nicholasen
dc.contributor.authorAgnantis, Niki J.en
dc.creatorZagorianakou, N.en
dc.creatorStefanou, D. G.en
dc.creatorMakrydimas, G.en
dc.creatorZagorianakou, P.en
dc.creatorBriassoulis, E. Chen
dc.creatorKaravasilis, V.en
dc.creatorPavlidis, Nicholasen
dc.creatorAgnantis, Niki J.en
dc.date.accessioned2018-06-22T09:53:34Z
dc.date.available2018-06-22T09:53:34Z
dc.date.issued2006
dc.identifier.urihttps://gnosis.library.ucy.ac.cy/handle/7/41912
dc.description.abstractMetallothioneins (MTs) are a family of cystein-rich metal-binding proteins, which are expressed in normal cells during fetal and postnatal life but also in a variety of human neoplasms. MT expression in human tumors has been linked to resistance to anticancer drugs and differentiation and progression in some types of tumors. This study examined the immunohistochemical expression of MTs in benign, borderline and malignant tumors of ovarian surface epithelium and the possible correlations with clinicopathological parameters and survival. A total of 87 cases with diagnosis of ovarian surface epithelial tumors were included. Specifically, 21 cases of benign cystadenomas (11 serous and 10 mucinous), 14 borderline (low malignant potential tumors, 8 mucinous and 6 serous) and 52 cases of ovarian cancer were analysed. Immunohistochemical expression of MT (cut-off level >10% of tumor cells) was clearly associated with malignancy. A statistically significant correlation was found between the expression of MT in cancer cases and benign tumors (p<0.0001) and cancer cases and borderline tumors p= 0.003. In cancer cases a difference was observed between grade I and III (p=0.002). There was no correlation of MT overexpression with survival in the small number of ovarian carcinoma patients where it was analysed. MT constitutes a marker that characterizes aggressiveness and a high malignant potential in ovarian epithelial tumors. In diagnostic problems MT may help distinguish between benign, borderline and malignant tumors.en
dc.language.isoengen
dc.sourceHistology and histopathologyen
dc.subjectArticleen
dc.subjectAntineoplastic agenten
dc.subjectHumanen
dc.subject80 and overen
dc.subjectAgeden
dc.subjectHumansen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectControlled studyen
dc.subjectFemaleen
dc.subjectMajor clinical studyen
dc.subjectDisease progressionen
dc.subjectOvarian canceren
dc.subjectOvarian neoplasmsen
dc.subjectOvary canceren
dc.subjectHuman tissueen
dc.subjectOvary tumoren
dc.subjectStatistical significanceen
dc.subjectSurvival rateen
dc.subjectAdolescenten
dc.subjectNeoplasticen
dc.subjectDisease courseen
dc.subjectCorrelation analysisen
dc.subjectClinical featureen
dc.subjectImmunohistochemistryen
dc.subjectProtein expressionen
dc.subjectCell proliferationen
dc.subjectProtein p53en
dc.subjectTumor suppressor protein p53en
dc.subjectGene expression regulationen
dc.subjectTumor differentiationen
dc.subjectHistopathologyen
dc.subjectDisease associationen
dc.subjectGene expression regulationen
dc.subjectPathologyen
dc.subjectTumor growthen
dc.subjectDiagnosisen
dc.subjectMiddle ageden
dc.subjectBiologicalen
dc.subjectTumor markersen
dc.subjectCarcinomaen
dc.subjectTumor markeren
dc.subjectDifferential diagnosisen
dc.subjectDifferentialen
dc.subjectGeneticsen
dc.subjectPhysiologyen
dc.subjectCell differentiationen
dc.subjectChemistryen
dc.subjectSerousen
dc.subjectEpithelium tumoren
dc.subjectCystadenomaen
dc.subjectCystadenomaen
dc.subjectMetallothioneinen
dc.subjectMetallothionein (mt)en
dc.subjectMucinousen
dc.titleClinicopathological study of metallothionein immunohistochemical expression, in benign, borderline and malignant ovarian epithelial tumorsen
dc.typeinfo:eu-repo/semantics/article
dc.description.volume21
dc.description.issue4-6
dc.description.startingpage341
dc.description.endingpage347
dc.author.facultyΙατρική Σχολή / Medical School
dc.author.departmentΙατρική Σχολή / Medical School
dc.type.uhtypeArticleen
dc.contributor.orcidPavlidis, Nicholas [0000-0002-2195-9961]
dc.contributor.orcidKaravasilis, V. [0000-0002-5806-9399]
dc.gnosis.orcid0000-0002-2195-9961
dc.gnosis.orcid0000-0002-5806-9399


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