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首页> 外文期刊>The international journal of biochemistry and cell biology >SOD2 is a C-myc target gene that promotes the migration and invasion of tongue squamous cell carcinoma involving cancer stem-like cells
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SOD2 is a C-myc target gene that promotes the migration and invasion of tongue squamous cell carcinoma involving cancer stem-like cells

机译:SOD2是C-myc靶基因,可促进涉及癌干样细胞的舌鳞癌的迁移和侵袭

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Our previous studies revealed that manganese superoxide dismutase (SOD2) contributes to the migration and invasion of tongue squamous cell carcinoma (TSCC). The purpose of the current study was to further clarify the mechanisms of SOD2 in the migration and invasion of TSCC. Side population (SP) cells were used as cancer stem-like cells and further assessed by sphere and colony formation assays, and the expression of stem cell markers (Bmi1, Nanog and ABCG2). We found that UM1 cells (TSCC cells with increased SOD2 expression, migration and invasion abilities) possessed a higher proportion of SP cells, sphere and colony formation, and expressed a higher level of stem cell markers compared to UM2 cells (reduced SOD2 expression, migration and invasion abilities). SOD2 expression as well as migration and invasion abilities were enhanced in SP cells compared to non-SP cells. Knockdown of SOD2 in UM1 cells or SP cells inhibited the migration and invasion abilities, reduced sphere and colony formation, and the expression of stem cell markers. Direct binding of the C-myc protein to the SOD2 promoter was demonstrated by chromatin immunoprecipitation and luciferase assays. Knockdown of C-myc in UM1 cells inhibited SOD2 expression as well as migration and invasion abilities. Our results indicate that cancer stem-like cells play an important role in the migration and invasion of TSCC. SOD2 is a direct target gene of C-myc and C-myc-SOD2-mediated migration and invasion of TSCC involve cancer stem-like cells. (C) 2015 Elsevier Ltd. All rights reserved.
机译:我们以前的研究表明,锰超氧化物歧化酶(SOD2)有助于舌鳞状细胞癌(TSCC)的迁移和侵袭。本研究的目的是进一步阐明SOD2在TSCC迁移和侵袭中的机制。侧群(SP)细胞用作癌症干细胞样细胞,并通过球体和集落形成测定法以及干细胞标志物(Bmi1,Nanog和ABCG2)的表达进行进一步评估。我们发现,与UM2细胞相比,UM1细胞(具有增加的SOD2表达,迁移和侵袭能力的TSCC细胞)具有更高比例的SP细胞,球体和集落形成,并表达了更高水平的干细胞标记(降低了SOD2表达,迁移和迁移)。和入侵能力)。与非SP细胞相比,SP细胞的SOD2表达以及迁移和侵袭能力均得到增强。敲低UM1细胞或SP细胞中的SOD2抑制了迁移和侵袭能力,减少了球体和集落的形成,并抑制了干细胞标志物的表达。 C-myc蛋白与SOD2启动子的直接结合通过染色质免疫沉淀和萤光素酶测定法得到证实。敲低UM1细胞中的C-myc抑制了SOD2的表达以及迁移和侵袭能力。我们的结果表明,癌干样细胞在TSCC的迁移和侵袭中起重要作用。 SOD2是C-myc和C-myc-SOD2介导的迁移的直接靶基因,TSCC的侵袭涉及癌干样细胞。 (C)2015 Elsevier Ltd.保留所有权利。

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