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dc.contributor.author김광현*
dc.date.accessioned2018-11-21T16:30:54Z-
dc.date.available2018-11-21T16:30:54Z-
dc.date.issued2018*
dc.identifier.issn1949-2553*
dc.identifier.otherOAK-21945*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/246900-
dc.description.abstractTo determine the suitability of serum endocan (ESM-1) levels for diagnosing and monitoring renal cell carcinoma (RCC), we measure serum ESM-1 levels in 56 RCC patients who had undergone radical or partial nephrectomies and 56 age- and sex-matched healthy kidney donors. Measurements were made before and 1 month and 3 months after surgery. The areas under the curve (AUCs) were determined from receiver operating characteristic (ROC) analyses. RCC patients had higher mean serum ESM-1 levels than control subjects (0.59 ± 0.07 vs. 0.52 ± 0.08 ng/mL, P < 0.001), with an AUC of 0.721 (95% CI: 0.628-0.817). In patients with tumors larger than 2 cm (n = 40) and those with clear-cell histology (n = 44), the AUCs for ESM-1 were 0.771 and 0.721, respectively. In control subjects, serum ESM-1 levels were higher in older (> 50 years) individuals (P < 0.001). Among the study cohort, the AUCs for ESM-1 were 0.813 in individuals 50 years of age or younger (n = 55) and 0.637 in individuals older than 50 years (n = 57). In RCC patients, serum ESM-1 levels were reduced 1 month (P = 0.047) and 3 months (P = 0.009) after surgery. These results suggest serum ESM-1 can serve as a serologic biomarker for diagnosing and monitoring RCC, particularly in patients younger than 50 years. © Kim et al.*
dc.description.sponsorshipYonsei University College of Medicine*
dc.languageEnglish*
dc.publisherImpact Journals LLC*
dc.subjectArea under curve*
dc.subjectCarcinoma*
dc.subjectEarly diagnosis*
dc.subjectRenal cell*
dc.titleClinical validation of serum endocan (ESM-1) as a potential biomarker in patients with renal cell carcinoma*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume9*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage662*
dc.relation.lastpage667*
dc.relation.journaltitleOncotarget*
dc.identifier.doi10.18632/oncotarget.23087*
dc.identifier.wosidWOS:000419615500053*
dc.identifier.scopusid2-s2.0-85040605957*
dc.author.googleKim K.H.*
dc.author.googleLee H.H.*
dc.author.googleYoon Y.E.*
dc.author.googleNa J.C.*
dc.author.googleKim S.Y.*
dc.author.googleCho Y.I.*
dc.author.googleHong S.J.*
dc.author.googleHan W.K.*
dc.contributor.scopusid김광현(57191527009)*
dc.date.modifydate20240222163024*


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