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dc.contributor.author홍영숙*
dc.contributor.author박혜영*
dc.date.accessioned2018-06-02T08:15:05Z-
dc.date.available2018-06-02T08:15:05Z-
dc.date.issued1997*
dc.identifier.issn0378-8512*
dc.identifier.otherOAK-17061*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/244385-
dc.description.abstractTo investigate whether transforming growth factor α (TGFα) treatment of human ovarian cancer cells was associated with the induction of c-myc protooncogene, the expression of this gene in NIH:OVCAR-3 cells was examined. TGFα induced increase in c-myc mRNA level, with a peak after 1 h of treatment; this stimulation was dose-dependent, with an optimal concentration of 5 ng/ml TGFα. Its primary action is probably at the transcription level since the half-life of c-myc mRNA measured in the presence of actinomycin D was not modified by TGFα treatment. In addition, TGFα stimulation of c-myc mRNA did not require protein synthesis since it was not suppressed by cycloheximide treatment. Antisense phosphorothioate oligonucleotide to c-myc specifically inhibited the TGFα-stimulated c-Myc protein expression and growth of NIH:OVCAR-3 cells. Our results indicate that induction of c-myc expression by TGFα plays an important role in the growth of NIH:OVCAR-3 cells.*
dc.languageEnglish*
dc.titleStimulation of c-myc protooncogene expression by transforming growth factor a in human ovarian cancer cells*
dc.typeArticle*
dc.relation.issue4*
dc.relation.volume29*
dc.relation.indexSCOPUS*
dc.relation.startpage203*
dc.relation.lastpage208*
dc.relation.journaltitleExperimental and Molecular Medicine*
dc.identifier.scopusid2-s2.0-0031593211*
dc.author.googleChoi J.-Y.*
dc.author.googleHong Y.-S.*
dc.author.googlePark H.-Y.*
dc.contributor.scopusid홍영숙(57218968598)*
dc.contributor.scopusid박혜영(7601567979)*
dc.date.modifydate20240301081003*
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의과대학 > 의학과 > Journal papers
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