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作 者:毛春蓉[1] 仲建新[2] 练云[1] 刘进[1] 王敏[1]
机构地区:[1]江苏省东台市人民医院妇产科,224200 [2]南通大学附属医院
出 处:《中国妇产科临床杂志》2013年第5期395-398,共4页Chinese Journal of Clinical Obstetrics and Gynecology
摘 要:目的探讨促性腺激素释放激素类似物(GnRHa)丙氨瑞林(Alarelin)与顺铂(DDP)对人卵巢癌耐药细胞CoC1/cDDP凋亡的影响。方法 CoC1/cDDP细胞分别加入不同浓度的丙氨瑞林及DDP+丙氨瑞林培养,设空白对照组(不加药),流式细胞仪检测亚G1期细胞及凋亡细胞和线粒体膜电位(ΔΨm),半定量RT-PCR法检测CoC1/cDDP细胞生存素(survivin)-⊿Ex3 mRNA及天冬氨酸特异性半胱氨酸蛋白酶(caspase-3mRNA的表达。采用四甲基偶氮唑蓝(MTT)法测定各组细胞生长抑制率。结果①随DDP浓度增加,亚G1期细胞及AnnexinV+/PI-细胞比例上升,对细胞的抑制作用增强(P<0.05)。丙氨瑞林作用于卵巢癌耐药细胞CoCl/cDDP后,随浓度增加降低ΔΨm,亚G1期细胞及AnnexinV+/PI-细胞比例增加,凋亡细胞增多,细胞增殖抑制率上升(P<0.01)。联合应用丙氨瑞林及10μg/ml DDP后,线粒体膜电位(ΔΨm)降低,Rh123-细胞数增加,G1期细胞及AnnexinV+/PI-细胞增多,细胞抑制率明显上升,强于单用DDP或丙氨瑞林;②丙氨瑞林单独或联合DDP作用于CoCl/cDDP细胞,caspase-3mRNA的表达随丙氨瑞林浓度增加而上调,但survinin-⊿Ex3mRNA表达无明显变化(P>0.05)。结论丙氨瑞林能促进凋亡,逆转CoCl/cDDP细胞对DDP耐药,其机制可能与降低ΔΨm,上调caspase-3mRNA表达有关。Objective To investigate the effect and the mechanisms of Alarelin combined with cisplatin(DDP)on the apoptosis in drug-resistant human ovarian cancer cell line CoC1/cDDP.Methods CoC1/cDDP cell were treated with different concentrations of alarelin,DDP and alarelin+DDP.The survivin-Ex3mRNA,caspase-3 mRNA were measured by RT-PCR.The G1cells and apoptosis cells and the cell mitochondrial membrane potential(ΔΨm)were measured by FCM.The growing inhibiting rates were examined by MTT.Results ① The apoptosis cells and the growing inhibiting rates increased with the concentration of DDP increased(P0.05).Alarelin increased the percentages of sub-G1and AnnexinV+/PI-cells in a dose-dependent manner(P0.01).Compared with separate use alarelin or DDP,after treating with alarelin+10μg/ml DDP,the apoptosis cells increased more obviously.The percentages of sub-G1,AnnexinV+/PI-cells and the percentages of Rh123cells were increased(P 0.01).②Alarelin significantly increased the expression of caspase-3mRNA in a dose-dependent manner(P 0.01),while treating with alarelin or alarelin combined with DDP,the expression of survivin-Ex3mRNA had no significant increased(P0.05).Conclusions Alarelin has strong reversal effects on DDP resistance in CoC1/cDDP,the effects may be related to decreasing theΔΨm and increasing expression of caspase-3mRNA.
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