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多西紫杉醇对人胃癌细胞株MKN-45的抑制及诱导凋亡作用的研究
作者:王彩莲1 陈宝安1 余卫平2 高峰3 宋萍3 
单位:1.东南大学,附属中大医院,江苏,南京,210009; 2.东南大学,基础医学院,江苏,南京,210009; 3.东南大学,临床医学院,江苏,南京,210009
关键词:人胃腺癌细胞株 多西紫杉醇 细胞增殖抑制 细胞凋亡 
分类号:R-332, R730.53, R735.2
出版年·卷·期(页码):2006·25·第四期(262-264)
摘要:

目的:研究多西紫杉醇对人胃腺癌MKN-45细胞的生长抑制作用及诱导人胃腺癌细胞凋亡作用.方法:采用MTT法测定细胞增殖抑制率,流式细胞技术检测细胞周期分布和凋亡率,应用电镜观察细胞凋亡的形态特点. 结果:(1) 多西紫杉醇在1.25~80μg·ml-1质量浓度范围内对MKN-45细胞株有抑制增殖作用,此作用与药物质量浓度呈正相关.(2)终质量浓度为20μg·ml-1的多西紫杉醇作用于MKN-45细胞8h有凋亡峰的出现,12h凋亡率接近50%.(3) 以20μg·ml-1的多西紫杉醇诱导MKN-45细胞凋亡3h和6h与未加药的对照组比较,可见MKN-45细胞周期被阻滞在G2/M期,S期比例减少.(4)20μg·ml-1的多西紫杉醇作用MKN-45细胞12h,可见典型的凋亡形态学改变.结论:多西紫杉醇可抑制人胃腺癌MKN-45细胞增殖,诱导MKN-45细胞凋亡.

Objective To study the inhibiting effect of docetaxel on the growth of human gastric cells(MKN-45) and the apoptosis induced by docetaxel in human gastric cells and its mechanism in inducing apoptosis.Methods MTT was used to detect the inhibition of cell proliferation.FCM was used to test the distribution of cell phases and the ratio of apoptosis.Electronic microscope was used to observe the configuration of the distribution of cell apoptosis.Results 1.The effective doses of docetaxel to inhibit the proliferation of human gastric cancer cells(MKN-45) was within the range of 1.25()μg·ml^{-1} to 80()μg·ml^{-1};and was positively correlated with the dosage.2.FCM test identified no apoptosis peak after 3()h to 6()h,but did after 8()h with the final dosage of docetaxel of 20()μg·ml^{-1}.The ratio of apotosis was close to 50% in 12()h.3.Compared with the control group,the arrest of cell phase was seen at phase G_2/M after induced for 3()h to 6()h with the dosage of docetaxel of 20()μg·ml^{-1} and the ratio of S phase was decreased.4.Typical morphological changes were seen in cells treated with docetaxel of 20()μg·ml^{-1} for 12()h.Conclusion The new generation of taxanes drug-docetaxel can inhibit the proliferation of MKN-45 and induce apoptosis.

参考文献:

[1] 王彩莲, 陈宝安. 多西紫杉醇治疗晚期胃癌的进展. 现代医学2005(1). doi:10.3969/j.issn.1671-7562.2005.01.023
[2] AJANI J A. Docetaxel for gastric and esophageal carcinomas, 2002
[3] LAVELLE F, FIZAMES C, GUéRITTE-VOEGELEIN F. Experimental properties of RP 56976,a Taxel derivative, 1989
[4] RIOU J F, NAUDIN A, LAVELLE F. Effects of Taxotere on murine and human tumour cell lines. 1992. doi:10.1016/S0006-291X(5)81474-3
[5] HILL B T, WHELAN R D H, SHELLARD S A. Differential cytotoxic effects of docetaxel in a range of mammalian tumour cell lines and certain drug resistant cell lines in vitro. 1994(12). doi:10.1007/BF00873957
[6] WIJKE H J, van CUTSEM E. Current treatments and future perspectives in colorectal and gastric cancer. 2003(2) 

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