Wyllie F S, Haughton M F, Rowson J M, Wynford-Thomas D
Department of Pathology, University of Wales College of Medicine, Cardiff, UK.
Br J Cancer. 1999 Mar;79(7-8):1111-20. doi: 10.1038/sj.bjc.6690177.
Differentiated thyroid carcinomas (in contrast to the rarer anaplastic form) are unusual among human cancers in displaying a remarkably low frequency of p53 mutation and appear to retain wild-type (wt) p53 function as assessed by the response of derived cell lines to DNA damage. Using one such cell line, K1, we have tested the effect of experimental abrogation of p53 function by generating matched sub-clones stably expressing either a neo control gene, a dominant-negative mutant p53 (143ala) or human papilloma virus protein HPV16 E6. Loss of p53 function in the latter two groups was confirmed by abolition of p53-dependent 'stress' responses including induction of the cyclin/CDK inhibitor p21WAF1 and G1/S arrest following DNA-damage. In contrast, no change was detected in the phenotype of 'unstressed' clones, with respect to any of the following parameters: proliferation rate in monolayer, serum-dependence for proliferation or survival, tumorigenicity, cellular morphology, or tissue-specific differentiation markers. The K1 line therefore represents a 'neutral' background with respect to p53 function, permitting the derivation of functionally p53 + or - clones which are not only iso-genic but also iso-phenotypic. Such a panel should be an ideal tool with which to test the p53-dependence of cellular stress responses, particularly the sensitivity to potential therapeutic agents, free from the confounding additional phenotypic differences which usually accompany loss of p53 function. The results also further support the hypothesis that p53 mutation alone is not sufficient to drive progression of thyroid cancer to the aggressive anaplastic form.
分化型甲状腺癌(与罕见的未分化型不同)在人类癌症中较为特殊,其p53突变频率极低,并且从衍生细胞系对DNA损伤的反应来看,似乎保留了野生型(wt)p53功能。利用其中一种细胞系K1,我们通过构建稳定表达新霉素对照基因、显性负性突变体p53(143ala)或人乳头瘤病毒蛋白HPV16 E6的匹配亚克隆,测试了实验性消除p53功能的效果。后两组中p53功能的丧失通过消除p53依赖性“应激”反应得以证实,包括细胞周期蛋白/周期蛋白依赖性激酶抑制剂p21WAF1的诱导以及DNA损伤后的G1/S期阻滞。相比之下,在“未受应激”的克隆中,未检测到以下任何参数的变化:单层增殖率、增殖或存活的血清依赖性、致瘤性、细胞形态或组织特异性分化标志物。因此,K1细胞系在p53功能方面代表了一个“中性”背景,允许衍生出功能上p53阳性或阴性的克隆,这些克隆不仅是同基因的,而且是同表型的。这样一组克隆应该是测试细胞应激反应对p53依赖性的理想工具,特别是对潜在治疗药物的敏感性,而不受通常伴随p53功能丧失的额外表型差异的干扰。这些结果也进一步支持了以下假说,即仅p53突变不足以促使甲状腺癌发展为侵袭性未分化型。