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pubmed-article:9299536pubmed:dateCreated1997-10-16lld:pubmed
pubmed-article:9299536pubmed:abstractTextThe mdr-1 gene has been shown to confer resistance to chemotherapy of multiple drugs which share no obvious structural similarities. We and others have previously reported that some virus-associated malignant cells express high levels of MDR-1 (1,2), probably regulated by some viral proteins. In this study we have examined the role of Tax, the key protein of HTLV-1. An excellent correlation was found between the existence of HTLV-1 and the expression of MDR-1 among seven human T-cell lines. In the second part of the study, a 1. 76-kb DNA fragment representing the upstream regulatory elements of human mdr-1 gene was cloned into the CAT reporter plasmid. When the Tax expression plasmid was co-transfected with the MDR-1 reporter plasmid, a significant induction of CAT activity was observed. We conclude that Tax protein may up-regulate the expression of the mdr-1 gene.lld:pubmed
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pubmed-article:9299536pubmed:statusMEDLINElld:pubmed
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pubmed-article:9299536pubmed:issn0006-291Xlld:pubmed
pubmed-article:9299536pubmed:authorpubmed-author:LinM TMTlld:pubmed
pubmed-article:9299536pubmed:authorpubmed-author:ChengA LALlld:pubmed
pubmed-article:9299536pubmed:authorpubmed-author:DoongS LSLlld:pubmed
pubmed-article:9299536pubmed:authorpubmed-author:ChuangS ESElld:pubmed
pubmed-article:9299536pubmed:copyrightInfoCopyright 1997 Academic Press.lld:pubmed
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pubmed-article:9299536pubmed:day18lld:pubmed
pubmed-article:9299536pubmed:volume238lld:pubmed
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pubmed-article:9299536pubmed:pagination482-6lld:pubmed
pubmed-article:9299536pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:9299536pubmed:year1997lld:pubmed
pubmed-article:9299536pubmed:articleTitleTax of the human T-lymphotropic virus type I transactivates promoter of the MDR-1 gene.lld:pubmed
pubmed-article:9299536pubmed:affiliationCancer Research Center, National Taiwan University College of Medicine, Taipei, Taiwan, Republic of China.lld:pubmed
pubmed-article:9299536pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9299536pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed