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dc.contributor.author筧, 善行ja
dc.contributor.author清川, 岳彦ja
dc.contributor.author橋村, 孝幸ja
dc.contributor.author吉田, 修ja
dc.contributor.alternativeKakehi, Yoshiyukien
dc.contributor.alternativeSegawa, Takehikoen
dc.contributor.alternativeHashimura, Takayukien
dc.contributor.alternativeYoshida, Osamuen
dc.date.accessioned2010-06-01T02:57:01Z-
dc.date.available2010-06-01T02:57:01Z-
dc.date.issued1992-11-
dc.identifier.issn0018-1994-
dc.identifier.urihttp://hdl.handle.net/2433/117691-
dc.description.abstractCep, およびSDB-ethylenediamine(N1379)の2剤について検討した。CepはP糖蛋白質の発現の高い腎癌細胞でVBLやADMに対して明らかな感受性増強効果を示したja
dc.description.abstractMost of renal cell carcinomas (RCCs) are refractory at the start of chemotherapy. We have demonstrated that the frequently elevated expression of the multidrug resistance gene (MDR) in RCCs is associated with the intrinsic vinca alkaloids and anthracyclines resistance. The preliminary clinical trials using verapamil or amiodarone in combination with vinblastine or doxorubicin to overcome multidrug-resistant (MDR) tumors could not achieve satisfactory results owing to severe cardiovascular toxicities of such reversing agents. In the present study, we studied the sensitizing ability of bis-benzyl-isoquinoline (cepharanthine) and SDB-ethylenediamine (N-1379) in natural MDR kidney cancer cells. Cepharanthine remarkably sensitized vinblastine and doxorubicin sensitivities in those cells with high MDR RNA levels. From a clinical point of view, cepharanthine seems to be a potent and less toxic agent to treat natural MDR kidney cancers.en
dc.format.mimetypeapplication/pdf-
dc.language.isojpn-
dc.publisher泌尿器科紀要刊行会ja
dc.subjectRenal canceren
dc.subjectMultidrug resistanceen
dc.subjectMDR-overcoming agentsen
dc.subject.ndc494.9-
dc.title腎細胞癌における内因性多剤耐性とその克服ja
dc.title.alternativeCircumvention of the intrinsic multidrug-resistance in renal cell carcinomaen
dc.typedepartmental bulletin paper-
dc.type.niitypeDepartmental Bulletin Paper-
dc.identifier.ncidAN00208315-
dc.identifier.jtitle泌尿器科紀要ja
dc.identifier.volume38-
dc.identifier.issue11-
dc.identifier.spage1319-
dc.identifier.epage1324-
dc.textversionpublisher-
dc.sortkey21-
dc.address国立姫路病院泌尿器科ja
dc.address国立姫路病院泌尿器科ja
dc.address京都大学医学部泌尿器科学教室ja
dc.address京都大学医学部泌尿器科学教室ja
dc.address.alternativethe Department of Urology, National Himeji Hospitalen
dc.address.alternativethe Department of Urology, National Himeji Hospitalen
dc.address.alternativethe Department of Urology, Kyoto University Faculty of Medicineen
dc.address.alternativethe Department of Urology, Kyoto University Faculty of Medicineen
dc.identifier.pmid1485588-
dcterms.accessRightsopen access-
dc.identifier.pissn0018-1994-
dc.identifier.jtitle-alternativeActa urologica Japonicala
dc.identifier.jtitle-alternativeHinyokika Kiyoen
出現コレクション:Vol.38 No.11

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