Beregovskaia N N, Maĭboroda R E, Skorbun A D
Biofizika. 1995 Jan-Feb;40(1):98-105.
A concept is advanced according to which the processes of ageing, non-specific pathology and malignant transformation are caused by mutations of mitochondrial DNA which controls protein synthesis of the oxidation phosphorylation system. A mathematical model is plotted for describing the efficiency of the system of energy supply of mammalian cells as a function of accumulation of mtDNA mutations. It is shown that at a definite degree of heterogeneity of mitochondria population malignant transformation proceeds. Explanations are presented of the existence of a latent period between the effect of cancerogenic agent and occurrence of tumour, mechanism of the realization of remote effects of chronic action of low intensity agents (these explanations are absent in modern theories of cancerogenesis and quantitative radiobiology).
提出了一个概念,即衰老、非特异性病理和恶性转化过程是由控制氧化磷酸化系统蛋白质合成的线粒体DNA突变引起的。绘制了一个数学模型来描述哺乳动物细胞能量供应系统的效率与线粒体DNA突变积累的函数关系。结果表明,当线粒体群体存在一定程度的异质性时,恶性转化就会发生。文中解释了致癌剂作用与肿瘤发生之间潜伏期的存在,以及低强度因素慢性作用的远程效应的实现机制(这些解释在现代癌症发生理论和定量放射生物学中并不存在)。