Meins F
Am J Pathol. 1977 Dec;89(3):687-702.
Crown-gall transformation involves the gradual and progressive activation of several biosynthetic capacities of the normal cell. These changes in cellular heredity, although extremely stable, are nonetheless potentially reversible and leave the cell totipotent. There is growing evidence that tumor-inducing principle is a self-replicating entity similar to a plasmid. Thus, it could be argued that tumor progression involves changes in the number or state of these entities in the cell. Studies of CDF habituation bear directly on this problem. Conversion of a cell division factor (CDF)-requiring normal cell to the CDF-autotrophic state is a key event in transformation. The fact that CDF habituation is progressive, occurs in the absence of agents of bacterial origin, and has an epigenetic basis indicates that it is not necessary to invoke either somatic mutation or the addition of foreign genes to account for tumor stability and progression in crown-gall. This conclusion provides further support for the hypothesis that, in the words of Braun,(78) "... the cancer problem is basically a problem of anomolous differentiation... Neoplastic growth, like developmental processes, stems from epigenetic modifications against a constant cellular genome."
冠瘿瘤转化涉及正常细胞几种生物合成能力的逐步激活。细胞遗传的这些变化虽然极其稳定,但仍有可能逆转,并且使细胞保持全能性。越来越多的证据表明,致瘤因子是一种类似于质粒的自我复制实体。因此,可以认为肿瘤进展涉及细胞中这些实体数量或状态的变化。对细胞分裂因子(CDF)适应性的研究直接涉及这个问题。将需要细胞分裂因子(CDF)的正常细胞转化为CDF自养状态是转化过程中的关键事件。CDF适应性是渐进性的,在没有细菌来源因子的情况下发生,并且具有表观遗传基础,这一事实表明,不必援引体细胞突变或外源基因的添加来解释冠瘿瘤中肿瘤的稳定性和进展。这一结论进一步支持了这样的假说,用布劳恩的话说,(78)“……癌症问题基本上是一个异常分化的问题……肿瘤生长,如同发育过程一样,源于针对恒定细胞基因组的表观遗传修饰。”