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首页> 外文期刊>Cancer gene therapy >Enhancement of adenoviral MDA-7-mediated cell killing in human lung cancer cells by geldanamycin and its 17-allyl- amino-17-demethoxy analogue
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Enhancement of adenoviral MDA-7-mediated cell killing in human lung cancer cells by geldanamycin and its 17-allyl- amino-17-demethoxy analogue

机译:格尔德霉素及其17-烯丙基-氨基-17-去甲氧基类似物增强腺病毒MDA-7介导的对人肺癌细胞的杀伤作用

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Our previous studies demonstrated that adenovirus-mediated overexpression of melanoma differentiation-associated gene-7 (Ad-mda7) leads to rapid induction of double-stranded RNA-dependent protein kinase (PKR) and activation of its downstream targets, resulting in apoptosis induction in human lung cancer cells. Here, we report that Ad-mda7 and the benzoquinone ansamycin geldanamycin (GA) interact in a highly synergistic manner to induce cell death in human lung cancer cells. Co-administration of Ad-mda7 and GA did not modify expression of MDA-7, and was not associated with further PKR induction and activation; instead the enhanced cytotoxicity of this combination was associated with inactivation of AKT by GA. By surface staining using anti-E-cadherin monoclonal antibody and flow cytometry, we found that treatment with the combination of Ad-mda7 and GA increased E-cadherin levels in these cancer cells. Ad-mda7 and GA cotreatment also inhibited lung cancer cell motility by increasing the |[beta]|-catenin|[sol]|E-cadherin association. Moreover, combination of GA derivative 17-allyl-amino, 17-demethoxygeldanamycin (17AAG), with Ad-mda7 resulted in enhancement of cell death in A549 and H460 human lung cancer cells.
机译:我们以前的研究表明,腺病毒介导的黑色素瘤分化相关基因7(Ad-mda7)的过度表达导致双链RNA依赖性蛋白激酶(PKR)的快速诱导和其下游靶标的活化,从而导致凋亡诱导。人肺癌细胞。在这里,我们报告Ad-mda7和苯醌安沙霉素格尔德霉素(GA)相互作用以高度协同的方式诱导人肺癌细胞死亡。 Ad-mda7和GA的共同给药不会改变MDA-7的表达,并且与进一步的PKR诱导和激活无关。相反,这种组合的增强的细胞毒性与GA灭活AKT有关。通过使用抗E-钙粘蛋白单克隆抗体的表面染色和流式细胞仪,我们发现Ad-mda7和GA的组合治疗可增加这些癌细胞中E-钙粘蛋白的水平。 Ad-mda7和GA协同治疗还通过增加|β| -catenin | [sol] | E-钙粘着蛋白的结合来抑制肺癌细胞的运动。而且,GA衍生物17-烯丙基-氨基,17-去甲氧基格尔德霉素(17AAG)与Ad-mda7的组合导致A549和H460人肺癌细胞的细胞死亡增加。

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