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Expression of ss-tubulin isotypes in classical Hodgkin's lymphoma

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dc.contributor.authorChoi, Jung-Woo-
dc.contributor.authorLee, Ju-Han-
dc.contributor.authorKim, Young-Sik-
dc.date.accessioned2021-09-06T21:36:08Z-
dc.date.available2021-09-06T21:36:08Z-
dc.date.created2021-06-18-
dc.date.issued2012-04-
dc.identifier.issn1320-5463-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/108779-
dc.description.abstractMicrotubules consist of heterodimers of a- and b-tubulin. Aberrant expression of specific b-tubulin isotype is associated with resistance to chemotherapy in malignant tumors. In this study, we examined the expressions of b-tubulin isotypes in classical Hodgkin's lymphoma (cHL) by immunohistochemistry. Among the b-tubulin isotypes, class II b-tubulin (31/34, 91%) was most frequently overexpressed in the cytoplasm of almost all Hodgkin's and Reed-Sternberg (HRS) cells, followed by class I b-tubulin (18/34, 53%) and class III b-tubulin (12/34, 35%). Class IV b-tubulin was not expressed in any cHL case. Class I b-tubulin was expressed in the background lymphoid cells as well as the HRS cells. Thus, our results indicate that class II b-tubulin may be very useful for immunohistochemical diagnosis of cHL, and provide valuable information for the potential application of b-tubulin isotype-specific targeting.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-BLACKWELL-
dc.subjectBINDING AGENTS-
dc.subjectBETA-TUBULIN-
dc.subjectCLASS-II-
dc.subjectRESISTANCE-
dc.subjectBIOLOGY-
dc.subjectCELLS-
dc.titleExpression of ss-tubulin isotypes in classical Hodgkin's lymphoma-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Jung-Woo-
dc.contributor.affiliatedAuthorLee, Ju-Han-
dc.contributor.affiliatedAuthorKim, Young-Sik-
dc.identifier.doi10.1111/j.1440-1827.2011.02785.x-
dc.identifier.scopusid2-s2.0-84862810270-
dc.identifier.wosid000302016700010-
dc.identifier.bibliographicCitationPATHOLOGY INTERNATIONAL, v.62, no.4, pp.287 - 290-
dc.relation.isPartOfPATHOLOGY INTERNATIONAL-
dc.citation.titlePATHOLOGY INTERNATIONAL-
dc.citation.volume62-
dc.citation.number4-
dc.citation.startPage287-
dc.citation.endPage290-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPathology-
dc.relation.journalWebOfScienceCategoryPathology-
dc.subject.keywordPlusBINDING AGENTS-
dc.subject.keywordPlusBETA-TUBULIN-
dc.subject.keywordPlusCLASS-II-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusBIOLOGY-
dc.subject.keywordPlusCELLS-
dc.subject.keywordAuthorHodgkin&apos-
dc.subject.keywordAuthors lymphoma-
dc.subject.keywordAuthormicrotubule-
dc.subject.keywordAuthortubulin-
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