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[以E2作为药物载体的定点化疗对人子宫内膜腺癌细胞的体外作用]

[The effects of site-directed chemotherapy due to E2 as a drug carrier to the human endometrial adenocarcinoma cells in vitro].

作者信息

Yoshizumi N

出版信息

Nihon Sanka Fujinka Gakkai Zasshi. 1985 Apr;37(4):637-45.

PMID:3989343
Abstract

The effects of Estracyt, a Nitrogen mustard (HN2) derivative of estradiol-17 beta versus the free HN2 on cell kinetics of the estrogen receptor positive human endometrial cancer cell line HEC-1 were investigated using flow cytometry. The results were as follows. The cell killing effects of Estracyt existed in a dependency on dose and time, whereas those of HN2 were dependent on dose alone. HN2 at 1 microgram/ml showed a marked increase in S phase and decrease in G0+1 phase. However, with equivalent doses of Estracyt at 10 micrograms/ml, even more remarkable was the accumulation in the G2+M phase. Synchronization at S phase with MTX showed no increase in sensitivity to these drugs on cells in S phase. Based on the above results, it was suggested that the free HN2 had an affect regardless of the cell cycle phase, whereas the effects of Estracyt corresponded to the cell cycle phase and Estracyt might have a fixed population of non-target cells existing in the G0+1 and S phase. Synchronization in the G1 phase with Sodium n-butylate could increase the target effects of Estracyt in S phase.

摘要

使用流式细胞术研究了雌二醇 - 17β的氮芥(HN2)衍生物雌莫司汀(Estracyt)与游离HN2对雌激素受体阳性人子宫内膜癌细胞系HEC - 1细胞动力学的影响。结果如下。雌莫司汀的细胞杀伤作用存在剂量和时间依赖性,而HN2的细胞杀伤作用仅依赖于剂量。1微克/毫升的HN2使S期显著增加,G0 + 1期减少。然而,对于10微克/毫升的等效剂量雌莫司汀,更显著的是G2 + M期的积累。用甲氨蝶呤(MTX)使细胞同步于S期并未显示S期细胞对这些药物的敏感性增加。基于上述结果,提示游离HN2对细胞周期各阶段均有影响,而雌莫司汀的作用与细胞周期阶段相关,并且雌莫司汀可能在G0 + 1期和S期存在一定数量的非靶细胞群体。用正丁酸钠使细胞同步于G1期可增加雌莫司汀在S期的靶向作用。

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