Koumenis C, Giaccia A
Department of Radiation Oncology, Stanford University School of Medicine, California 94305, USA.
Mol Cell Biol. 1997 Dec;17(12):7306-16. doi: 10.1128/MCB.17.12.7306.
Studies have indicated that deregulated oncogene expression can result in either programmed cell death or proliferation, depending on the cellular microenvironment. However, little is known about whether oncogenic signals in themselves are able to activate a cellular apoptotic program. We have tested the hypothesis that oncogenic signals in the absence of gene expression are sufficient to induce cell death, which would indicate that constitutive expression of antiapoptotic genes is necessary for maintenance of the transformed state. Using two highly specific RNA polymerase (RNAP) II inhibitors, 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB) and alpha-amanitin, which inhibit RNAP II function by two distinct mechanisms, we found that inhibition of gene expression substantially increased apoptosis in a time- and dose-dependent manner in p53+/+- and p53(-/-)-transformed mouse embryonic fibroblasts and in HeLa cells, demonstrating that this type of apoptosis does not require wild-type p53. Engineered expression of an alpha-amanitin resistance RNAP II gene rendered cells resistant to induction of apoptosis by alpha-amanitin without affecting their sensitivity to DRB, indicating that alpha-amanitin induces apoptosis solely by inhibiting RNAP II function and not by a nonspecific mechanism. DRB-induced apoptosis was independent of the cell cycle or ongoing DNA replication, since DRB induced similar levels of apoptosis in asynchronous cells and cells synchronized by collection at mitosis. Inhibition of RNAP II in untransformed cells like Rat-1 or human AG1522 fibroblasts resulted not in apoptosis but in growth arrest. In contrast, deregulated expression of c-Myc in Rat-1 cells dramatically increased their sensitivity to DRB, directly demonstrating that apoptosis following inhibition of RNAP II function is greatly enhanced by oncogenic expression. The requirement for RNAP II function to prevent oncogene-induced apoptosis implies the need for the constitutive expression of an antiapoptotic gene(s) to maintain the transformed state. The differential sensitivities of untransformed and transformed cells to induction of apoptosis by transcriptional inhibition, coupled with the finding that this type of apoptosis is independent of p53 status, suggest that inhibition of RNAP II may be exploited therapeutically for the design of successful antitumor agents.
研究表明,癌基因表达失调可导致程序性细胞死亡或增殖,这取决于细胞微环境。然而,关于致癌信号本身是否能够激活细胞凋亡程序,人们所知甚少。我们检验了这样一个假设:在不存在基因表达的情况下,致癌信号足以诱导细胞死亡,这将表明抗凋亡基因的组成型表达对于维持转化状态是必要的。使用两种高度特异性的RNA聚合酶(RNAP)II抑制剂,5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)和α-鹅膏蕈碱,它们通过两种不同机制抑制RNAP II功能,我们发现抑制基因表达在p53+/+-和p53(-/-)-转化的小鼠胚胎成纤维细胞以及HeLa细胞中以时间和剂量依赖性方式显著增加凋亡,表明这种类型的凋亡不需要野生型p53。工程化表达α-鹅膏蕈碱抗性RNAP II基因使细胞对α-鹅膏蕈碱诱导的凋亡产生抗性,而不影响它们对DRB的敏感性,表明α-鹅膏蕈碱仅通过抑制RNAP II功能而非非特异性机制诱导凋亡。DRB诱导的凋亡与细胞周期或正在进行的DNA复制无关,因为DRB在异步细胞和通过有丝分裂收集同步化的细胞中诱导相似水平的凋亡。在未转化的细胞如Rat-1或人AG1522成纤维细胞中抑制RNAP II不会导致凋亡而是导致生长停滞。相反,Rat-1细胞中c-Myc的失调表达显著增加了它们对DRB的敏感性,直接证明致癌表达大大增强了抑制RNAP II功能后的凋亡。防止癌基因诱导凋亡对RNAP II功能的需求意味着需要抗凋亡基因的组成型表达来维持转化状态。未转化和转化细胞对转录抑制诱导凋亡的不同敏感性,以及这种类型的凋亡与p53状态无关的发现,表明抑制RNAP II可能在治疗上被用于设计成功的抗肿瘤药物。