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与千金藤素联合使用增强抗癌剂对B16黑色素瘤细胞的作用——II. 抗代谢物、烷化剂、亚硝基脲

[Enhancement of the effects of anticancer agents on B16 melanoma cells by combination with cepharanthine--II. Antimetabolite, alkylating agent, nitrosourea].

作者信息

Kubota R, Kubota K, Yamada S

机构信息

Dept. of Radiology & Nuclear Medicine, Tohoku University, Sendai, Japan.

出版信息

Gan To Kagaku Ryoho. 1992 Nov;19(13):2169-74.

PMID:1444482
Abstract

We have studied chemotherapy enhancement by the combination of the biscoclaurine alkaloid, Cepharanthine (Ceph), using the inhibition of colony forming efficiency (CFE) of B16 melanoma cells in vitro. Hydroxyurea, antimetabolite, showed a time-dependent inhibition of CFE, and the combination with Ceph enhanced CFE inhibition by 29%, which is stable and independent of the treatment time. Dacarbazine, a biological alkylating agent, given with Ceph showed a time-dependent inhibition of CFE (43%). MCNU, a nitrosourea, with Ceph showed the greatest inhibition of CFE (67%) among the anticancer agents used. The CFE inhibition was time-dependent and required a higher concentration of MCNU. In this series of studies using CFE inhibition of B16 melanoma cells in vitro, etoposide showed the best effect by the combination with Ceph, which seems to be a candidate for in vivo evaluation.

摘要

我们利用体外抑制B16黑色素瘤细胞集落形成效率(CFE)的方法,研究了双苄基异喹啉生物碱汉防己甲素(Ceph)联合使用时对化疗的增强作用。抗代谢药羟基脲对CFE有时间依赖性抑制作用,与Ceph联合使用时,CFE抑制作用增强了29%,且该增强作用稳定,与处理时间无关。生物烷化剂达卡巴嗪与Ceph联合使用时,对CFE有时间依赖性抑制作用(43%)。亚硝基脲类药物甲环亚硝脲与Ceph联合使用时,在所使用的抗癌药物中对CFE的抑制作用最强(67%)。CFE抑制作用具有时间依赖性,且需要更高浓度的甲环亚硝脲。在这一系列利用体外抑制B16黑色素瘤细胞CFE的研究中,依托泊苷与Ceph联合使用时效果最佳,似乎是体内评估的一个候选药物。

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