首页> 外文期刊>Technology in cancer research & treatment. >Upregulation of FoxM1 by MnSOD Overexpression Contributes to Cancer Stem-Like Cell Characteristics in the Lung Cancer H460 Cell Line
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Upregulation of FoxM1 by MnSOD Overexpression Contributes to Cancer Stem-Like Cell Characteristics in the Lung Cancer H460 Cell Line

机译:MnSOD过量表达对FoxM1的上调有助于肺癌H460细胞系中的癌干细胞特性

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Manganese superoxide dismutase promotes migration and invasion in lung cancer cells via upregulation of the transcription factor forkhead box M1. Here, we assessed whether upregulation of forkhead box M1 by manganese superoxide dismutase overexpression mediates the acquisition of cancer stem-like cell characteristics in non-small cell lung cancer H460 cells. The second-generation spheroids from H460 cells were used as lung cancer stem-like cells. The levels of manganese superoxide dismutase, forkhead box M1, stemness markers (CD133, CD44, and ALDH1), and transcription factors (Bmi1, Nanog, and Sox2) were analyzed by Western blot. Sphere formation in vitro and carcinogenicity of lung cancer stem-like cells were evaluated by spheroid formation assay and limited dilution xenograft assays. Knockdown or overexpression of manganese superoxide dismutase or/and forkhead box M1 by transduction with short hairpin RNA(shRNA) or complementary DNA were performed for mechanistic studies. We showed that manganese superoxide dismutase and forkhead box M1 amounts as well as the expression levels of stemness markers and transcription factors sphere formation in vitro, and carcinogenicity of lung cancer stem-like cells were higher than in monolayer cells. Lung cancer stem-like cells transduced with manganese superoxide dismutase shRNA or FoxM1 shRNA exhibited decreased sphere formation and lower amounts of stemness markers and transcription factors. Overexpression of manganese superoxide dismutase or FoxM1 in H460 cells resulted in elevated sphere formation rates and protein levels of stemness markers and transcription factors. Meanwhile, manganese superoxide dismutase knockdown or overexpression accordingly altered forkhead box M1 levels. However, forkhead box M1 knockdown or overexpression had no effect on manganese superoxide dismutase levels but inhibited or promoted lung cancer stem-like cell functions. Interestingly, forkhead box M1 overexpression alleviated the inhibitory effects of manganese superoxide dismutase knockdown in lung cancer stem-like cells. In a panel of non-small cell lung cancer cells, including H441, H1299, and H358 cells, compared to the respective monolayer counterparts, the expression levels of manganese superoxide dismutase and forkhead box M1 were elevated in the corresponding spheroids. These findings revealed the role of forkhead box M1 upregulation by manganese superoxide dismutase overexpression in maintaining lung cancer stem-like cell properties. Therefore, inhibition of forkhead box M1 upregulation by manganese superoxide dismutase overexpression may represent an effective therapeutic strategy for non-small cell lung cancer.
机译:锰超氧化物歧化酶通过上调转录因子叉头盒M1促进肺癌细胞的迁移和侵袭。在这里,我们评估了锰超氧化物歧化酶过表达对叉头箱M1的上调是否介导了非小细胞肺癌H460细胞中癌干样细胞特性的获得。 H460细胞的第二代球体被用作肺癌干细胞样细胞。通过蛋白质印迹分析了锰超氧化物歧化酶,叉头盒M1,茎标记(CD133,CD44和ALDH1)和转录因子(Bmi1,Nanog和Sox2)的水平。通过球体形成测定和有限稀释异种移植测定评估了体外球形成和肺癌干样细胞的致癌性。通过短发夹RNA(shRNA)或互补DNA的转导来敲除或超表达锰超氧化物歧化酶或/和叉头盒M1进行机理研究。我们发现锰超氧化物歧化酶和叉头盒M1的数量以及干细胞标志物和转录因子球形成的表达水平在体外,肺癌干样细胞的致癌性高于单层细胞。用锰超氧化物歧化酶shRNA或FoxM1 shRNA转导的肺癌干样细胞显示出减少的球体形成和较低的茎干标记和转录因子。锰超氧化物歧化酶或FoxM1在H460细胞中的过表达导致球形成率提高以及茎标记和转录因子的蛋白水平升高。同时,锰超氧化物歧化酶的敲低或过表达相应地改变了叉头箱M1的水平。但是,叉头盒M1的敲低或过表达对锰超氧化物歧化酶水平没有影响,但抑制或促进了肺癌干样细胞功能。有趣的是,叉头盒M1的过表达减轻了锰超氧化物歧化酶敲除对肺癌干样细胞的抑制作用。与相应的单层对应物相比,在一组包括H441,H1299和H358细胞的非小细胞肺癌细胞中,锰超氧化物歧化酶和叉头盒M1的表达水平在相应的球体中升高。这些发现揭示了锰超氧化物歧化酶过表达导致叉头箱M1上调在维持肺癌干细胞样细胞特性中的作用。因此,锰超氧化物歧化酶过表达抑制叉头箱M1上调可能代表了非小细胞肺癌的有效治疗策略。

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