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拓扑替康在依赖于给药方案的过程中增加拓扑异构酶IIα水平并提高对依托泊苷治疗的敏感性。

Topotecan increases topoisomerase IIalpha levels and sensitivity to treatment with etoposide in schedule-dependent process.

作者信息

Whitacre C M, Zborowska E, Gordon N H, Mackay W, Berger N A

机构信息

Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106-4937, USA.

出版信息

Cancer Res. 1997 Apr 15;57(8):1425-8.

PMID:9108439
Abstract

To elucidate the effect of topoisomerase (Topo) I inhibitors in the modulation of Topo II levels and sensitivity to Topo II-directed drugs, athymic mice bearing SW480 human colon cancer xenografts were treated with simultaneous, subsequent, or distant doses of topotecan and etoposide. This in vivo study demonstrates that simultaneous administration of topotecan and etoposide results in an antagonistic response. In contrast, inhibition of Topo I by topotecan results in a compensatory increase in Topo II alpha levels associated with increasing sensitivity of tumors to subsequent treatment with the Topo II inhibitor etoposide. Furthermore, we show that Topo II alpha levels decline 5 days after the last dose of topotecan, resulting in restoration of the original response of the xenografts to etoposide. Thus, this study emphasizes the critical role of schedule dependency to optimize the effectiveness of combination chemotherapy with Topo I and Topo II inhibitors.

摘要

为阐明拓扑异构酶(Topo)I抑制剂在调节Topo II水平及对Topo II靶向药物敏感性方面的作用,对携带SW480人结肠癌异种移植瘤的无胸腺小鼠同时、先后或间隔给予拓扑替康和依托泊苷进行治疗。这项体内研究表明,同时给予拓扑替康和依托泊苷会产生拮抗反应。相反,拓扑替康对Topo I的抑制导致Topo IIα水平的代偿性增加,这与肿瘤对随后使用Topo II抑制剂依托泊苷治疗的敏感性增加相关。此外,我们发现最后一剂拓扑替康给药5天后Topo IIα水平下降,导致异种移植瘤对依托泊苷的原始反应恢复。因此,本研究强调了给药方案依赖性在优化Topo I和Topo II抑制剂联合化疗有效性方面的关键作用。

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