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2-甲氧基雌二醇对SNO食管癌细胞的细胞形态和Cdc2激酶活性的体外作用

In vitro effects of 2-methoxyestradiol on cell morphology and Cdc2 kinase activity in SNO oesophageal carcinoma cells.

作者信息

Joubert Annie, Marais Sumari

机构信息

Department of Physiology, University of Pretoria, Pretoria, South Africa.

出版信息

Cell Biochem Funct. 2007 May-Jun;25(3):357-62. doi: 10.1002/cbf.1409.

Abstract

The effects of 1 x 10(-6) M exogenous 2-methoxyestradiol (2 ME) were determined on cell morphology and cell division cycle (Cdc) 2 kinase activity in SNO oesophageal carcinoma cells. Mitotic indices revealed an increase in metaphase cells (11.2%) when compared to the 0.5% vehicle-treated cells after 18 h of exposure to 2 ME. Vehicle-treated control cells did not show any hallmarks of apoptosis after 18 h of exposure to dimethyl sulphoxide. Only 0.5% of 2 ME-treated cells showed characteristics of apoptosis. Conversely, increased morphological hallmarks of apoptosis were observed in SNO-treated cells after 21.5 h of 2 ME exposure. When compared to the 0.5% in vehicle-treated cells, 4.7% of cells were in apoptosis. Furthermore, 34.1% of cells were blocked in metaphase after 21.5 h of 2 ME exposure compared to 0.6% of vehicle-control cells. In addition, Cdc2 kinase activity was statistically significantly increased (1.3-fold) (p<0.005) in 2 ME-treated cells when compared to vehicle-treated controls. The present preliminary study suggests that the accumulation observed in metaphase cells and the increase in Cdc2 kinase activity caused by 2 ME are consistent with morphological hallmarks of mitotic arrest and disrupted mitotic spindle formation, thus leading to induction of apoptosis in SNO cells.

摘要

研究了1×10⁻⁶ M外源性2-甲氧基雌二醇(2 ME)对SNO食管癌细胞的细胞形态和细胞分裂周期(Cdc)2激酶活性的影响。有丝分裂指数显示,在暴露于2 ME 18小时后,与0.5%溶媒处理的细胞相比,中期细胞增加(11.2%)。暴露于二甲基亚砜18小时后,溶媒处理的对照细胞未显示任何凋亡特征。仅0.5%的2 ME处理细胞显示出凋亡特征。相反,在暴露于2 ME 21.5小时后的SNO处理细胞中观察到凋亡的形态学特征增加。与溶媒处理细胞中的0.5%相比,4.7%的细胞发生凋亡。此外,暴露于2 ME 21.5小时后,34.1%的细胞停滞在中期,而溶媒对照细胞为0.6%。此外,与溶媒处理的对照相比,2 ME处理细胞中的Cdc2激酶活性在统计学上显著增加(1.3倍)(p<0.005)。本初步研究表明,2 ME导致的中期细胞积累和Cdc2激酶活性增加与有丝分裂停滞和有丝分裂纺锤体形成破坏的形态学特征一致,从而导致SNO细胞凋亡。

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