Kawabe Shinichiro, Nishikawa Takashi, Munshi Anupama, Roth Jack A, Chada Sunil, Meyn Raymond E
Department of Experimental Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, Texas 77030, USA.
Mol Ther. 2002 Nov;6(5):637-44.
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.
我们检测了腺病毒介导的黑色素瘤分化相关基因7(Ad-mda-7)对非小细胞肺癌(NSCLC)细胞系(A549(野生型TP53/野生型RB1)和H1299(缺失型TP53/野生型RB1))以及正常人肺成纤维细胞(NHLF)系(CCD-16和MRC-9)的放射增敏能力。克隆形成试验结果表明,Ad-mda7增强了NSCLC细胞的放射敏感性,且与它们的TP53基因状态无关。另一方面,NHLF细胞系似乎对Ad-mda7的细胞毒性作用相对耐药,与NSCLC细胞相比未表现出放射增敏。我们进一步研究了与正常细胞相比,Ad-mda7对NSCLC细胞放射增敏能力存在差异的原因。NSCLC细胞系中辐射诱导的凋亡得以恢复,但正常细胞系中未恢复。蛋白质印迹分析显示,Ad-mda7增强放射敏感性与上调NSCLC细胞中Fas或Bax表达的能力无关。进一步分析表明,Ad-mda7使A549和H1299细胞中磷酸化c-Jun表达增加,但在CCD-16细胞中未增加。这些结果支持将Ad-mda7基因替代与放射治疗联合用于NSCLC的治疗。