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拓扑替康单药及联合化疗方案的时间依赖性细胞毒性。

Schedule-dependent cytotoxicity of topotecan alone and in combination chemotherapy regimens.

作者信息

Cheng M F, Chatterjee S, Berger N A

机构信息

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

出版信息

Oncol Res. 1994;6(6):269-79.

PMID:7865902
Abstract

The schedule-dependent cytotoxic effects of topotecan were evaluated in tissue culture experiments with Chinese hamster V79 cells. One hour exposure to topotecan resulted in a typical phase-specific cell killing curve in which increasing concentrations kill progressively more cells and then reach a plateau when all susceptible cells are killed. In contrast, exposure for 24 h results in a steep concentration-response curve with no plateau. Other S-phase agents such as hydroxyurea or aphidicolin antagonized cytotoxicity when administered by simultaneous exposure with topotecan. Combinations of melphalan, BCNU (1,3 bis(2-chloroethyl)-1-nitrosourea), or cisplatinum with topotecan were most effective when cells were exposed to the alkylating agent or platinating agent during the first hour of a 24-h topotecan exposure. Combinations of topotecan with etoposide or adriamycin produce more cytotoxicity when topotecan is administered by prolonged exposure; however, there is no significant difference depending on whether the topoisomerase II inhibitor is added at the beginning or end of the topotecan exposure. These studies show the importance of appropriate dose scheduling to obtain optimal interaction of chemotherapeutic agents given in combination with topotecan.

摘要

在使用中国仓鼠V79细胞的组织培养实验中评估了拓扑替康的时间依赖性细胞毒性作用。用拓扑替康处理1小时会产生典型的时相特异性细胞杀伤曲线,即随着浓度增加,杀伤的细胞逐渐增多,当所有易感细胞被杀死后达到平台期。相比之下,处理24小时会产生一条陡峭的浓度 - 反应曲线,没有平台期。其他S期作用药物,如羟基脲或阿非迪霉素,与拓扑替康同时给药时会拮抗细胞毒性。当在24小时拓扑替康处理的第一小时内使细胞暴露于美法仑、卡莫司汀(1,3 - 双(2 - 氯乙基)-1 - 亚硝基脲)或顺铂时,它们与拓扑替康的联合最为有效。当长时间给予拓扑替康时,拓扑替康与依托泊苷或阿霉素的联合产生更大的细胞毒性;然而,拓扑异构酶II抑制剂在拓扑替康处理开始时或结束时添加,细胞毒性没有显著差异。这些研究表明了合适的给药时间安排对于获得与拓扑替康联合使用的化疗药物的最佳相互作用的重要性。

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