Takai Noriyuki, Ueda Tami, Nishida Masakazu, Nasu Kaei, Narahara Hisashi
Department of Obstetrics and Gynecology, Oita University Faculty of Medicine, Hasama-machi, Yufu-shi, Oita 879-5593, Japan.
Int J Mol Med. 2008 Jan;21(1):109-15.
We investigated the effect of five histone deacetylase inhibitors (HDACIs) on the choriocarcinoma cell line, BeWo. BeWo cells were treated with various concentrations of five HDACIs, and their effects on cell growth, cell cycle, apoptosis, and related measurements were investigated. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assays showed that the BeWo choriocarcinoma cell line was sensitive to the growth inhibitory effect of five HDACIs. Cell cycle analysis indicated that exposure to HDACIs decreased the proportion of cells in the S-phase and increased the proportion in the G0/G1 phases of the cell cycle. Induction of apoptosis was confirmed by annexin V staining of externalized phosphatidylserine and loss of the transmembrane potential of mitochondria. This induction occurred in concert with altered expression of genes related to cell growth, malignant phenotype, and apoptosis. Furthermore, HDACI treatment of this cell line increased acetylation of H3 and H4 histone tails. These results raise the possibility that HDACIs may prove particularly effective in the treatment of choriocarcinoma.
我们研究了五种组蛋白去乙酰化酶抑制剂(HDACIs)对绒毛膜癌细胞系BeWo的影响。用不同浓度的五种HDACIs处理BeWo细胞,并研究它们对细胞生长、细胞周期、凋亡及相关指标的影响。3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑蓝检测表明,BeWo绒毛膜癌细胞系对五种HDACIs的生长抑制作用敏感。细胞周期分析表明,暴露于HDACIs会降低S期细胞比例,增加细胞周期G0/G1期的比例。通过膜联蛋白V对外化磷脂酰丝氨酸的染色及线粒体跨膜电位的丧失证实了凋亡的诱导。这种诱导与细胞生长、恶性表型和凋亡相关基因表达的改变同时发生。此外,用HDACIs处理该细胞系会增加H3和H4组蛋白尾部的乙酰化。这些结果增加了HDACIs可能在绒毛膜癌治疗中特别有效的可能性。