Chen M J, Holskin B, Strickler J, Gorniak J, Clark M A, Johnson P J, Mitcho M, Shalloway D
Department of Molecular Genetics, Smith Kline and French Laboratories, King of Prussia, Pennsylvania 19406.
Nature. 1987;330(6148):581-3. doi: 10.1038/330581a0.
Tumour necrosis factor alpha (ref. 1), synthesized primarily by monocytes in response to various invasive agents, induces a wide variety of biological effects relevant to regulating cell growth and differentiation, including the selective killing of some tumour cells and the growth stimulation of some normal fibroblasts. As tumour necrosis factor (TNF) appears to kill tumour cells preferentially, we asked whether TNF sensitivity correlates with the expression of specific oncogene(s). If so, by examining the cellular target(s) of the oncogene product, it might be possible to identify specific factor(s) which mediate TNF action. By using an in vitro cytotoxicity assay with NIH 3T3 and Fisher BRK-derived cells expressing exogenously introduced oncogenes, we found that adenovirus E1A proteins induce susceptibility to TNF killing.
肿瘤坏死因子α(参考文献1)主要由单核细胞响应各种侵袭性因子而合成,可诱导多种与调节细胞生长和分化相关的生物学效应,包括选择性杀伤某些肿瘤细胞以及刺激某些正常成纤维细胞生长。由于肿瘤坏死因子(TNF)似乎优先杀伤肿瘤细胞,我们不禁要问,TNF敏感性是否与特定癌基因的表达相关。如果是这样,通过检查癌基因产物的细胞靶点,或许能够识别介导TNF作用的特定因子。通过使用体外细胞毒性试验,对表达外源导入癌基因的NIH 3T3细胞和Fisher BRK衍生细胞进行检测,我们发现腺病毒E1A蛋白可诱导细胞对TNF杀伤的敏感性。