Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/32926
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dc.date.accessioned2023-06-06T06:23:15Z-
dc.date.available2023-06-06T06:23:15Z-
dc.date.issued2015-11-22-
dc.identifier.citationAtalay, F. Ö. vd. (2016). "Significance of amyloid A immunoexpression in the prognosis of renal cell carcinoma". APMIS, 124(4), 257-262.en_US
dc.identifier.issn0903-4641-
dc.identifier.issn1600-0463-
dc.identifier.urihttps://doi.org/10.1111/apm.12499-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1111/apm.12499-
dc.identifier.urihttp://hdl.handle.net/11452/32926-
dc.description.abstractThe study investigated immunoexpression of amyloid A (AA) in clear cell renal cell carcinoma (CCRCC) and evaluated its clinicopathologic correlation, particularly in disease progression. Expression of AA protein was evaluated in patients with CCRCC by immunohistochemistry. 146 cancerous tissue samples from 86 male and 60 female patients were studied. The relationship between AA protein expression and TNM stage, nuclear grade, renal capsule invasion, perirenal invasion, and survival of the patients were assessed. Thirty four percent of CCRCC cases were AA positive. The positive AA immunoexpression was related to higher Fuhrman nuclear grade, presence of perirenal invasion of the tumor, and poor survival of patients with CCRCC. There was not any statistically significant difference between patients' gender, status of capsule invasion, and stages of the tumor in terms of AA immunoexpression. Tumor stage (Hazard ratio (HR) = 7.76 (95% CI: 2.43-24.8) for stage 3 and HR = 29.9 (95% CI: 6.97-128.32) for stage 4) and AA immunoexpression (HR = 2.16 (95% CI: 1.01-4.64) were found to be associated with survival of the patients with CCRCC in Cox regression analysis. Immunoexpression of AA was increased in high grade CCRCCs. Immunoexpression of AA was associated with poor survival in patients with CCRCC. Thus, AA staining might be used as a useful immunohistological marker for the prediction of poor prognosis in renal cell cancer.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectImmunologyen_US
dc.subjectMicrobiologyen_US
dc.subjectPathologyen_US
dc.subjectAmyloid Aen_US
dc.subjectPerirenal invasionen_US
dc.subjectPrognosisen_US
dc.subjectRenal cell carcinomaen_US
dc.subjectStageen_US
dc.subjectSurvival serumen_US
dc.subjectSAAen_US
dc.subjectProteinen_US
dc.subjectCanceren_US
dc.subjectProteomicsen_US
dc.subjectLungen_US
dc.subject.meshAdulten_US
dc.subject.meshAgeden_US
dc.subject.meshAged, 80 and overen_US
dc.subject.meshBiomarkers, tumoren_US
dc.subject.meshCarcinoma, renal cellen_US
dc.subject.meshFemaleen_US
dc.subject.meshGene expressionen_US
dc.subject.meshHumansen_US
dc.subject.meshImmunohistochemistryen_US
dc.subject.meshKidneyen_US
dc.subject.meshKidney neoplasmsen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshNeoplasm gradingen_US
dc.subject.meshNeoplasm invasivenessen_US
dc.subject.meshNeoplasm stagingen_US
dc.subject.meshNephrectomyen_US
dc.subject.meshPrognosisen_US
dc.subject.meshProportional hazards modelsen_US
dc.subject.meshSerum amyloid A proteinen_US
dc.titleSignificance of amyloid A immunoexpression in the prognosis of renal cell carcinomaen_US
dc.typeArticleen_US
dc.identifier.wos000372895700003tr_TR
dc.identifier.scopus2-s2.0-84954158599tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Cerrahi Patoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Üroloji Anabilim Dalı.tr_TR
dc.identifier.startpage257tr_TR
dc.identifier.endpage262tr_TR
dc.identifier.volume124tr_TR
dc.identifier.issue4tr_TR
dc.relation.journalAPMISen_US
dc.contributor.buuauthorAtalay, Fatma Öz-
dc.contributor.buuauthorVuruşkan, Berna Aytaç-
dc.contributor.buuauthorVuruşkan, Hakan-
dc.contributor.researcheridAAH-9746-2021tr_TR
dc.identifier.pubmed26750935tr_TR
dc.subject.wosImmunologyen_US
dc.subject.wosMicrobiologyen_US
dc.subject.wosPathologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4 (Immunology)en_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid15623010600tr_TR
dc.contributor.scopusid57053559100tr_TR
dc.contributor.scopusid6507328150tr_TR
dc.subject.scopusProtein; Amyloidosis; Amyloid Enhancing Factoren_US
dc.subject.emtreeAmyloid A proteinen_US
dc.subject.emtreeSerum amyloid Aen_US
dc.subject.emtreeTumor markeren_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeCancer prognosisen_US
dc.subject.emtreeCancer stagingen_US
dc.subject.emtreeCancer survivalen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDisease courseen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman tissueen_US
dc.subject.emtreeImmunohistochemistryen_US
dc.subject.emtreeImmunoreactivityen_US
dc.subject.emtreeKidney carcinomaen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeOverall survivalen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeCancer gradingen_US
dc.subject.emtreeCarcinoma, renal cellen_US
dc.subject.emtreeGene expressionen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeKidneyen_US
dc.subject.emtreeKidney neoplasmsen_US
dc.subject.emtreeMetabolismen_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeMortalityen_US
dc.subject.emtreeNephrectomyen_US
dc.subject.emtreePathologyen_US
dc.subject.emtreePrognosisen_US
dc.subject.emtreeProportional hazards modelen_US
dc.subject.emtreeTumor invasionen_US
dc.subject.emtreeVery elderlyen_US
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