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7-顺式-O-甲基诺加罗醇对中国仓鼠卵巢细胞DNA合成、存活及细胞周期进程的影响。

Effect of 7-con-O-methylnogarol on DNA synthesis, survival, and cell cycle progression of Chinese hamster ovary cells.

作者信息

Adams E G, Crampton S L, Bhuyan B K

出版信息

Cancer Res. 1981 Dec;41(12 Pt 1):4981-7.

PMID:6458356
Abstract

The effect of 7-con-O-methylnogarol (7-OMEN) on the survival of exponentially growing and plateau-phase Chinese hamster ovary cells was determined in a cloning assay. After 2 hr of exposure, the 50% lethal dose for exponential and plateau-phase cells was 0.3 and 1.5 microgram/ml, respectively. Drug doses for cell progression studies were based upon drug lethality; therefore, higher doses were used for plateau than for exponential populations. The effect of 7-OMEN on cell progression was studied by DNA flow cytometry under the following conditions: (a) during 24 hr of continuous exposure of exponentially growing cells; (b) during recovery of exponential cells after 2 or 7 hr of drug exposure; and (c) during recovery of plateau-phase cells after 2 hr of exposure. Exponential cells exposed continuously for 24 hr progressed normally from M to G1 phase and from G1 to S phase, progression through S phase was slowed, and cells were ultimately blocked in G2 + M. Inhibition of S-phase progression was dose dependent, 0.2 microgram/ml having only slight effect and 1.0 microgram/ml accumulating a large fraction in S phase. Inhibition of S-phase progression correlated with DNA synthesis inhibition. Similar inhibitory effects were observed after pulsed (2- or 7-hr) exposure of exponential cells. 7-OMEN also blocked plateau-phase cells in G2 + M after 2 hr of exposure, but higher doses (3.0 microgram/ml) were required. Simultaneous exposure of exponential cells to Colcemid (which blocks cells in metaphase) and 1.0 microgram 7-OMEN per ml completely inhibited the expected increase in mitotic index, indicating that the G2 + M block observed by DNA flow cytometry was a block in G2 or prophase.

摘要

在克隆试验中测定了7-顺式-O-甲基诺加罗醇(7-OMEN)对指数生长期和平稳期中国仓鼠卵巢细胞存活的影响。暴露2小时后,指数生长期细胞和平稳期细胞的50%致死剂量分别为0.3和1.5微克/毫升。用于细胞进程研究的药物剂量基于药物致死率;因此,平稳期细胞使用的剂量高于指数生长期细胞。在以下条件下,通过DNA流式细胞术研究了7-OMEN对细胞进程的影响:(a)指数生长期细胞连续暴露24小时期间;(b)药物暴露2或7小时后指数生长期细胞恢复期间;(c)暴露2小时后平稳期细胞恢复期间。连续暴露24小时的指数生长期细胞正常地从M期进入G1期,从G1期进入S期,S期进程减慢,细胞最终停滞在G2+M期。S期进程的抑制呈剂量依赖性,0.2微克/毫升只有轻微影响,1.0微克/毫升使很大一部分细胞积聚在S期。S期进程的抑制与DNA合成抑制相关。指数生长期细胞脉冲(2或7小时)暴露后观察到类似的抑制作用。暴露2小时后,7-OMEN也使平稳期细胞停滞在G2+M期,但需要更高的剂量(3.0微克/毫升)。指数生长期细胞同时暴露于秋水仙酰胺(使细胞停滞在中期)和每毫升1.0微克7-OMEN完全抑制了预期的有丝分裂指数增加,表明通过DNA流式细胞术观察到的G2+M期停滞是在G2期或前期的停滞。

相似文献

1
Effect of 7-con-O-methylnogarol on DNA synthesis, survival, and cell cycle progression of Chinese hamster ovary cells.7-顺式-O-甲基诺加罗醇对中国仓鼠卵巢细胞DNA合成、存活及细胞周期进程的影响。
Cancer Res. 1981 Dec;41(12 Pt 1):4981-7.
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Cancer Res. 1988 Jan 1;48(1):109-16.

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Invest New Drugs. 1984;2(4):359-67. doi: 10.1007/BF00171586.
2
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Invest New Drugs. 1987;5(3):219-29. doi: 10.1007/BF00175291.
3
Cytotoxicity of combinations of prostaglandin D2 (PGD2) and antitumor drugs for B16 melanoma cells in culture.
Invest New Drugs. 1986;4(4):315-23. doi: 10.1007/BF00173504.
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Invest New Drugs. 1985;3(3):233-44. doi: 10.1007/BF00179427.
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J Cell Biol. 1988 Feb;106(2):415-22. doi: 10.1083/jcb.106.2.415.
6
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Invest New Drugs. 1991 Nov;9(4):349-51. doi: 10.1007/BF00183579.
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Invest New Drugs. 1991 Aug;9(3):261-2. doi: 10.1007/BF00176980.
8
Adozelesin, a potent new alkylating agent: cell-killing kinetics and cell-cycle effects.
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