Experimental combination chemotherapy of pirarubicin with various antitumor drugs against P388 murine leukemia.

Cancer biochemistry biophysics Pub Date : 1994-09-01
H Izumi, S Hirano, Y Matsushita, H Iguchi, H Tone, T Takeuchi
{"title":"Experimental combination chemotherapy of pirarubicin with various antitumor drugs against P388 murine leukemia.","authors":"H Izumi,&nbsp;S Hirano,&nbsp;Y Matsushita,&nbsp;H Iguchi,&nbsp;H Tone,&nbsp;T Takeuchi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>We have examined the therapeutic effects of combination therapy of pirarubicin ((2\"R)-4'-O-tetrahydropyranyladriamycin, THP) with various antitumor agents against P388 murine leukemia. THP showed a high antitumor activity in combination with various antitumor drugs, especially with cyclophosphamide (CPM), cisplatin (CDDP), mitomycin C (MMC), enocitabine (BHAC), vindesine (VDS) or methotrexate (MTX). The effects of combination therapy depended on the order of administration of THP and combined drugs. THP-preceding treatment gave more synergistic effects in combination with 5-fluorouracil (5-FU) or MTX. THP-preceding or simultaneous treatment with etoposide (ETP) indicated the higher synergistic activity than ETP-preceding one. Moreover, THP showed much higher synergistic effects in any order of the combination with CPM, CDDP, MMC, BHAC, VDS or MTX. These results suggest that THP possesses a therapeutic usefulness clinically in combination with various antitumor drugs, if the selection of drugs combined with THP and the order of administration are suitable.</p>","PeriodicalId":9552,"journal":{"name":"Cancer biochemistry biophysics","volume":"14 2","pages":"137-49"},"PeriodicalIF":0.0000,"publicationDate":"1994-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer biochemistry biophysics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

We have examined the therapeutic effects of combination therapy of pirarubicin ((2"R)-4'-O-tetrahydropyranyladriamycin, THP) with various antitumor agents against P388 murine leukemia. THP showed a high antitumor activity in combination with various antitumor drugs, especially with cyclophosphamide (CPM), cisplatin (CDDP), mitomycin C (MMC), enocitabine (BHAC), vindesine (VDS) or methotrexate (MTX). The effects of combination therapy depended on the order of administration of THP and combined drugs. THP-preceding treatment gave more synergistic effects in combination with 5-fluorouracil (5-FU) or MTX. THP-preceding or simultaneous treatment with etoposide (ETP) indicated the higher synergistic activity than ETP-preceding one. Moreover, THP showed much higher synergistic effects in any order of the combination with CPM, CDDP, MMC, BHAC, VDS or MTX. These results suggest that THP possesses a therapeutic usefulness clinically in combination with various antitumor drugs, if the selection of drugs combined with THP and the order of administration are suitable.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
吡柔比星联合多种抗肿瘤药物治疗P388小鼠白血病的实验研究。
我们研究了吡柔比星((2 ' R)-4'- o -四氢吡喃ladriamycin, THP)与各种抗肿瘤药物联合治疗P388小鼠白血病的疗效。THP与多种抗肿瘤药物联用,特别是与环磷酰胺(CPM)、顺铂(CDDP)、丝裂霉素C (MMC)、依诺他滨(BHAC)、长春地西(VDS)或甲氨蝶呤(MTX)联用,均显示出较高的抗肿瘤活性。联合治疗的效果取决于THP和联合用药的给药顺序。thp治疗前联合5-氟尿嘧啶(5-FU)或MTX具有更强的协同作用。在thp之前或与ETP同时处理时,显示出比ETP之前更高的协同活性。此外,THP在与CPM、CDDP、MMC、BHAC、VDS或MTX联合的任何顺序中均表现出更高的协同效应。这些结果表明,如果THP与各种抗肿瘤药物联合使用的药物选择和给药顺序合适,THP在临床上具有治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Lactoferrin expression in human breast cancer. Modulation of the impaired drug metabolism in sarcoma-180-bearing mice by echitamine chloride. Magnetic field induced inhibition of human osteosarcoma cells treated with adriamycin. Modulating effect of new potential antimelanomic agents, spin-labeled triazenes and nitrosoureas on the DOPA-oxidase activity of tyrosinase. Molecular basis of specific inhibition of urokinase plasminogen activator by amiloride.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1