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Clinical, histological, and immunohistochemical features predicting 1p/19q loss of heterozygosity in oligodendroglial tumors

DC Field Value Language
dc.contributor.author김세훈-
dc.contributor.author김태승-
dc.contributor.author김호근-
dc.date.accessioned2017-10-26T06:30:37Z-
dc.date.available2017-10-26T06:30:37Z-
dc.date.issued2005-
dc.identifier.issn0001-6268-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/150896-
dc.description.abstractTo identify a better diagnostic criteria for oligodendroglial tumors, we investigated the clinical, histological, and immunohistochemical features that would be able to predict a 1p/19q loss of heterozygosity (LOH) in these tumors. We performed a PCR-based LOH test with the 1p and 19q microsatellite markers by microdissecting tumor in 56 samples (44 oligodendrogliomas and 12 mixed oligoastrocytomas) of paraffin-embedded tissue. Patients with oligodendroglial tumors with 1p/19q LOH had a statistically significant better prognosis for overall survival. Comparative analysis of several features indicated that the 1p/19q LOH tumors were associated with two histological features, “tumor cellularity” and “perinuclear halo,” and low O 6-methylguanine-DNA-methyltransferase (MGMT) expression and high cytoplasmic glutathione S-transferase pi (GST-π) expression. In addition, the incidence of 1p/19q LOH was infrequent in the youngest age category (less than 20 years old) studied. Using the new features, we could predict the 1p/19q status of oligodendroglial tumors with greater than 90% accuracy. Therefore, applying these features in clinical practice, would be helpful in clarifying oligodendroglial tumor diagnosis.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherSpringer-
dc.relation.isPartOfACTA NEUROCHIRURGICA-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHAge Factors-
dc.subject.MESHAged-
dc.subject.MESHBiomarkers, Tumor/analysis*-
dc.subject.MESHBrain Neoplasms/diagnosis*-
dc.subject.MESHBrain Neoplasms/genetics*-
dc.subject.MESHBrain Neoplasms/metabolism-
dc.subject.MESHChild-
dc.subject.MESHChromosomes, Human, Pair 1-
dc.subject.MESHChromosomes, Human, Pair 19-
dc.subject.MESHFemale-
dc.subject.MESHGlioma/diagnosis*-
dc.subject.MESHGlioma/genetics*-
dc.subject.MESHGlioma/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHImmunohistochemistry-
dc.subject.MESHLoss of Heterozygosity-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPolymerase Chain Reaction-
dc.subject.MESHSensitivity and Specificity-
dc.subject.MESHSurvival Analysis-
dc.titleClinical, histological, and immunohistochemical features predicting 1p/19q loss of heterozygosity in oligodendroglial tumors-
dc.typeArticle-
dc.publisher.locationGermany-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pathology (병리학교실)-
dc.contributor.departmentDept. of Pathology (병리학교실)-
dc.contributor.departmentDept. of Pathology (병리학교실)-
dc.contributor.googleauthorSe Hoon Kim-
dc.contributor.googleauthorHoguen Kim-
dc.contributor.googleauthorTai Seung Kim-
dc.identifier.doi10.1007/s00401-005-1020-x-
dc.contributor.localIdA00610-
dc.contributor.localIdA01071-
dc.contributor.localIdA01183-
dc.relation.journalcodeJ00018-
dc.identifier.eissn0942-0940-
dc.identifier.pmid15920661-
dc.identifier.urlhttp://link.springer.com/article/10.1007%2Fs00401-005-1020-x-
dc.subject.keywordOligodendroglioma-
dc.subject.keywordChromosomes human pair 1-
dc.subject.keywordChromosomes human pair 19-
dc.subject.keywordLoss of heterozygosity-
dc.subject.keywordHistology-
dc.contributor.alternativeNameKim, Se Hoon-
dc.contributor.alternativeNameKim, Tai Seung-
dc.contributor.alternativeNameKim, Ho Keun-
dc.citation.volume110-
dc.citation.number1-
dc.citation.startPage27-
dc.citation.endPage38-
dc.identifier.bibliographicCitationACTA NEUROCHIRURGICA, Vol.110(1) : 27-38, 2005-
dc.date.modified2017-05-04-
dc.identifier.rimsid42742-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers

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