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作 者:葛雅琨[1] 张元新[1] 陈云鹏[2] 柏旭[2] 施维[3]
机构地区:[1]吉林化工学院环境与生物工程学院,132022 [2]吉林大学组合化学与新药创制研究中心,132022 [3]分子酶学工程教育部重点实验室,132022
出 处:《中华肿瘤杂志》2012年第2期100-103,共4页Chinese Journal of Oncology
基 金:吉林省科委重点项目(20080932);长春市科技计划项目(长科合2006224)
摘 要:目的研究新型Nutlins类似物NL-608在体外诱导乳腺癌MCF-7细胞凋亡的作用,并初步探讨其可能的凋亡通路。方法采用四甲基偶氮唑蓝(MTT)法检测NL-608化合物对MCF-7细胞增殖的影响;采用流式细胞仪(FCM)检测NL-608诱导MCF-7细胞凋亡情况;采用Westernblot方法检测多聚ADP-核糖聚合酶(PARP)、半胱天冬酶(pro-caspase3、pro-caspase8、pro-caspase9)以及Fas和Fas配体(FasL)的变化,并利用活力检测试剂盒检测caspase3、caspase8、caspase9的活力。结果NL-608对MCF-7细胞的增殖具有抑制作用,并呈浓度依赖性,100、33、11、3.7、1.2、0.4、0.14Ixmol/LNL-608作用后,MCF-7细胞的存活率分别为(6.70±1.27)%、(10.90±5.08)%、(24.31±3.77)%、(45.144±5.14)%、(79.16±10.01)%、(97.00±2.31)%和(99.90±0.01)%。随着NL-608浓度的增加,PARP被切割,pro-caspase3和pro—caspase8的Westernblot条带变淡,但pro-caspase9的条带无变化。活力测定结果进一步显示,easpase3和caspase8被激活,其相对活力与对照组相比分别为(3.76±0.35)倍和(2.71±0.27)倍;而caspase9的相对活力为(1.03±0.08)倍,即对easpase9无明显影响。Westernblot结果显示,Fas和FasL的表达量均随NL-608浓度的增加而增加。结论NL-608化合物能够有效地在体外诱导MCF-7细胞凋亡,且可能依赖于easpase3和caspase8相关的死亡受体凋亡途径,为进一步研发乳腺癌治疗药物奠定了实验基础。Objective To observe the effect of NL-608 (a nutlin analog) on apoptosis induction in human breast cancer MCF-7 cells in vitro, and investigate the relevant molecular mechanism. Methods The effect of NL-608 on proliferation of MCF-7 cells was determined by MTI" assay. The apoptosis in MCF-7 cells was determined by flow cytometry with annexin V-FITC and PI. The activity of caspase 3, caspase 8 and caspase 9 was determined with caspase activity assay kit and Western blot, and the proteins of Fas and FasL were determined by Western blot. Results NL-608 showed a dose-dependent inhibitory effect on the proliferation of MCF-7 cells. It induced apoptosis in MCF-7 cells in a dose-dependent manner. The activity of caspase 3 and easpase 8 in MCF-7 cells was increased with the increasing concentration of NL-608, but caspase 9 had no changes. The proteins of Fas and FasL were increased in a dose-dependent manner. Conclusion NL-608 induces apoptosis in MCF-7 cells in vitro through inducing caspase 3 activity and death receotor-mediated signal oathwav.
关 键 词:乳腺肿瘤 MCF-7细胞 Nutlins类似物 凋亡
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