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38_1319.pdf | 4.66 MB | Adobe PDF | 見る/開く |
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DCフィールド | 値 | 言語 |
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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.alternative | Kakehi, Yoshiyuki | en |
dc.contributor.alternative | Segawa, Takehiko | en |
dc.contributor.alternative | Hashimura, Takayuki | en |
dc.contributor.alternative | Yoshida, Osamu | en |
dc.date.accessioned | 2010-06-01T02:57:01Z | - |
dc.date.available | 2010-06-01T02:57:01Z | - |
dc.date.issued | 1992-11 | - |
dc.identifier.issn | 0018-1994 | - |
dc.identifier.uri | http://hdl.handle.net/2433/117691 | - |
dc.description.abstract | Cep, 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.abstract | Most 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.mimetype | application/pdf | - |
dc.language.iso | jpn | - |
dc.publisher | 泌尿器科紀要刊行会 | ja |
dc.subject | Renal cancer | en |
dc.subject | Multidrug resistance | en |
dc.subject | MDR-overcoming agents | en |
dc.subject.ndc | 494.9 | - |
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.alternative | Circumvention of the intrinsic multidrug-resistance in renal cell carcinoma | en |
dc.type | departmental bulletin paper | - |
dc.type.niitype | Departmental Bulletin Paper | - |
dc.identifier.ncid | AN00208315 | - |
dc.identifier.jtitle | 泌尿器科紀要 | ja |
dc.identifier.volume | 38 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 1319 | - |
dc.identifier.epage | 1324 | - |
dc.textversion | publisher | - |
dc.sortkey | 21 | - |
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.alternative | the Department of Urology, National Himeji Hospital | en |
dc.address.alternative | the Department of Urology, National Himeji Hospital | en |
dc.address.alternative | the Department of Urology, Kyoto University Faculty of Medicine | en |
dc.address.alternative | the Department of Urology, Kyoto University Faculty of Medicine | en |
dc.identifier.pmid | 1485588 | - |
dcterms.accessRights | open access | - |
dc.identifier.pissn | 0018-1994 | - |
dc.identifier.jtitle-alternative | Acta urologica Japonica | la |
dc.identifier.jtitle-alternative | Hinyokika Kiyo | en |
出現コレクション: | Vol.38 No.11 |

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