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A Comparison of Gene Expression Profiles between Primary Human AML Cells and Therapy-related AML Cells

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dc.contributor.authorKim, Young Hun-
dc.contributor.authorKim, Hyung-Soo-
dc.contributor.authorHwang, Junmo-
dc.contributor.authorLee, Jinseok-
dc.contributor.authorKim, Seonggon-
dc.contributor.authorPark, So-Young-
dc.contributor.authorChang, Kyu-Tae-
dc.contributor.authorKim, Kil Soo-
dc.contributor.authorRyoo, Zae Young-
dc.contributor.authorLee, Sanggyu-
dc.date.accessioned2021-09-09T02:16:08Z-
dc.date.available2021-09-09T02:16:08Z-
dc.date.created2021-06-10-
dc.date.issued2008-12-
dc.identifier.issn1976-9148-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/122360-
dc.description.abstractTo identify genes whose expression correlated with biological features of therapy-related AML (t-AML), we analyzed the expression profiles of de novo AML t(9;11) and t-AML t(9;11) bone marrow samples using previously published SAGE data. Three-hundred twenty-nine transcripts that satisfied statistical (P<0.05) and magnitude-of-change (>= 4-fold) criteria were identified as differentially expressed between de novo AML t(9;11) and t-AML t(9;11) cells. Of these transcripts, 301 (91%) matched known genes or ESTs and were classified according to functional categorlies (http://david.abcc.ncifcrf.gov/). The majority of differentially expressed genes in t-AML t(9;11) were involved in the regulation of biological and metabolic processes. Especially prominent among these were genes related to immune and drug responses. These results establish a framework for developing new drugs for the treatment of t-AML.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.subjectACUTE MYELOID-LEUKEMIA-
dc.subjectPROTEIN-
dc.subjectAPOPTOSIS-
dc.subjectMYELODYSPLASIA-
dc.subjectTRANSLOCATIONS-
dc.subjectSUPPRESSION-
dc.subjectMECHANISMS-
dc.subjectGROWTH-
dc.subjectDOMAIN-
dc.titleA Comparison of Gene Expression Profiles between Primary Human AML Cells and Therapy-related AML Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, So-Young-
dc.identifier.doi10.4062/biomolther.2008.16.4.431-
dc.identifier.scopusid2-s2.0-69549129355-
dc.identifier.wosid000262747300019-
dc.identifier.bibliographicCitationBIOMOLECULES & THERAPEUTICS, v.16, no.4, pp.431 - 436-
dc.relation.isPartOfBIOMOLECULES & THERAPEUTICS-
dc.citation.titleBIOMOLECULES & THERAPEUTICS-
dc.citation.volume16-
dc.citation.number4-
dc.citation.startPage431-
dc.citation.endPage436-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001300641-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusACUTE MYELOID-LEUKEMIA-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusMYELODYSPLASIA-
dc.subject.keywordPlusTRANSLOCATIONS-
dc.subject.keywordPlusSUPPRESSION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusDOMAIN-
dc.subject.keywordAuthorTherapy-related AML-
dc.subject.keywordAuthorGene expression-
dc.subject.keywordAuthorSAGE-
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