Oya Natsuo, Zölzer Friedo, Werner Frank, Streffer Christian
Institute for Medical Radiation Biology, University Hospital Essen, Germany.
Strahlenther Onkol. 2003 Feb;179(2):99-106. doi: 10.1007/s00066-003-0973-8.
The effects of serum starvation on radiation sensitivity, cell proliferation and apoptosis were investigated with particular consideration of the p53 status.
Four human tumor cell lines, Be11 (melanoma, p53 wild-type), MeWo (melanoma, p53 mutant), 4197 (squamous cell carcinoma, p53 wild-type) and 4451 (squamous cell carcinoma, p53 mutant), were used. After the cells had been incubated in starvation medium (0.5% FCS) for 1-6 days, changes in cell cycle distribution, induction of apoptosis and necrosis, and changes in radiation sensitivity were assessed by two-parameter flow cytometric measurements of DNA-dye-exclusion/Annexin V binding, and a conventional colony assay, respectively.
p53 wild-type cell lines showed a decrease in the BrdU labeling index and an increase in the apoptotic cell frequency in starvation medium. p53 mutant cell lines showed a decrease in the BrdU labeling index but no evidence of apoptosis. These cells went into necrosis instead. The radiation sensitivity was increased in 4451 and slightly decreased in Be11 and 4197 in starvation medium.
These data suggest a functional involvement of p53 in starvation-induced G1-block and apoptosis in tumor cells. Altered radiosensitivity after culture in starvation medium seemed to be explained at least in part by the starvation-induced G1-block. The frequency of starvation-induced apoptosis or necrosis was not correlated with radiation sensitivity.
研究血清饥饿对辐射敏感性、细胞增殖和凋亡的影响,并特别考虑p53状态。
使用四种人类肿瘤细胞系,即Be11(黑色素瘤,p53野生型)、MeWo(黑色素瘤,p53突变型)、4197(鳞状细胞癌,p53野生型)和4451(鳞状细胞癌,p53突变型)。细胞在饥饿培养基(0.5%胎牛血清)中孵育1 - 6天后,分别通过DNA染料排除/膜联蛋白V结合的双参数流式细胞术测量以及传统的集落形成试验评估细胞周期分布的变化、凋亡和坏死的诱导情况以及辐射敏感性的变化。
p53野生型细胞系在饥饿培养基中BrdU标记指数降低,凋亡细胞频率增加。p53突变型细胞系BrdU标记指数降低,但无凋亡迹象,这些细胞反而发生坏死。在饥饿培养基中,4451的辐射敏感性增加,Be11和4197的辐射敏感性略有降低。
这些数据表明p53在肿瘤细胞饥饿诱导的G1期阻滞和凋亡中发挥功能性作用。饥饿培养基培养后辐射敏感性的改变似乎至少部分可以由饥饿诱导的G1期阻滞来解释。饥饿诱导的凋亡或坏死频率与辐射敏感性无关。