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首页> 外文期刊>Molecular therapy: the journal of the American Society of Gene Therapy >Adenovirus-mediated mda-7 gene expression radiosensitizes non-small cell lung cancer cells via TP53-independent mechanisms.
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Adenovirus-mediated mda-7 gene expression radiosensitizes non-small cell lung cancer cells via TP53-independent mechanisms.

机译:腺病毒介导的mda-7基因表达通过不依赖TP53的机制放射增敏非小细胞肺癌细胞。

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We examined the ability of adenoviral-mediated expression of the melanoma differentiation associated gene-7 (Ad-mda-7), to radiosensitize non-small cell lung cancer (NSCLC) cell lines (A549 (wt-TP53/wt-RB1) and H1299 (del-TP53/wt-RB1)), and normal human lung fibroblast (NHLF) lines (CCD-16 and MRC-9). Results of clonogenic assays indicated that Ad-mda7 enhanced the radiosensitivity of the NSCLC cells independent of their TP53 gene status. On the other hand, the NHLF cell lines seemed to be relatively resistant to the cytotoxic effects of Ad-mda7 and were not radiosensitized compared with the NSCLC cells. We further examined the basis for this difference in the ability of Ad-mda7 to radiosensitize NSCLC cells compared with normal cells. Radiation-induced apoptosis was restored in the NSCLC lines, but not in the normal lines. Western blot analysis revealed that Ad-mda7 enhances radiosensitivity independently of any ability to upregulate the expression of Fas or Bax in NSCLC cells. Further analysis indicated that phosphorylated c-Jun expression was increased by Ad-mda7 in both A549 and H1299 cells, but not in CCD-16 cells. These results support the use of gene replacement with Ad-mda7 in combination with radiotherapy for the treatment of NSCLC.
机译:我们检查了黑色素瘤分化相关基因7(Ad-mda-7)的腺病毒介导的表达对非小细胞肺癌(NSCLC)细胞系(A549(wt-TP53 / wt-RB1)和H1299(del-TP53 / wt-RB1))和正常人肺成纤维细胞(NHLF)系(CCD-16和MRC-9)。克隆形成试验的结果表明,Ad-mda7增强了NSCLC细胞的放射敏感性,而与它们的TP53基因状态无关。另一方面,与NSCLC细胞相比,NHLF细胞系似乎对Ad-mda7的细胞毒性作用具有相对抗性,并且没有放射致敏作用。我们进一步检查了与正常细胞相比,Ad-mda7对NSCLC细胞放射增敏能力差异的基础。辐射诱导的细胞凋亡在NSCLC细胞系中得以恢复,但在正常细胞系中未恢复。蛋白质印迹分析表明,Ad-mda7可以增强放射敏感性,而与任何在NSCLC细胞中上调Fas或Bax表达的能力无关。进一步的分析表明,Ad-mda7在A549和H1299细胞中均可磷酸化c-Jun表达,而在CCD-16细胞中则不会。这些结果支持使用Ad-mda7替代基因并结合放射疗法治疗NSCLC。

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