Ames B N, Shigenaga M K, Gold L S
Division of Biochemistry and Molecular Biology, University of California, Berkeley 94720.
Environ Health Perspect. 1993 Dec;101 Suppl 5(Suppl 5):35-44. doi: 10.1289/ehp.93101s535.
DNA lesions that escape repair have a certain probability of giving rise to mutations when the cell divides. Endogenous DNA damage is high: 10(6) oxidative lesions are present per rat cell. An exogenous mutagen produces an increment in lesions over the background rate of endogenous lesions. The effectiveness of a particular lesion depends on whether it is excised by a DNA repair system and the probability that it gives rise to a mutation when the cell divides. When the cell divides, an unrepaired DNA lesion has a certain probability of giving rise to a mutation. Thus, an important factor in the mutagenic effect of an exogenous agent whether it is genotoxic or non-genotoxic, is the increment it causes over the background cell division rate (mitogenesis) in cells that appear to matter most in cancer, the stem cells, which are not on their way to being discarded. Increasing their cell division rate increases mutation and therefore cancer. There is little cancer from nondividing cells. Endogenous cell division rates can be influenced by hormone levels, decreased by calorie restriction, or increased by high doses of chemicals. If both the rate of DNA lesions and cell division are increased, then there will be a multiplicative effect on mutagenesis (and carcinogenesis), for example, by high doses of a mutagen that also increases mitogenesis through cell killing. The defense system against reactive electrophilic mutagens, such as the glutathione transferases, are also almost all inducible and buffer cells against increments in active forms of chemicals that can cause DNA lesions. A variety of DNA repair defense systems, almost all inducible, buffer the cell against any increment in DNA lesions. Therefore, the effect of a particular chemical insult depends on the level of each defense, which in turn depends on the past history of exposure. Exogenous agents can influence the induction and effectiveness of these defenses. Defenses can be partially disabled by lack of particular micronutrients in the diet (e.g., antioxidants).
逃避修复的DNA损伤在细胞分裂时有一定概率引发突变。内源性DNA损伤程度很高:每只大鼠细胞中存在10⁶个氧化性损伤。外源性诱变剂会使损伤数量在内源性损伤的背景发生率之上有所增加。特定损伤的有效性取决于它是否能被DNA修复系统切除,以及细胞分裂时其引发突变的概率。当细胞分裂时,未修复的DNA损伤有一定概率引发突变。因此,对于一种外源性物质(无论其是否具有基因毒性)的诱变效应而言,一个重要因素是它在对癌症似乎最为关键的细胞(即干细胞,这些细胞并非即将被淘汰)中,相对于背景细胞分裂速率(有丝分裂)所导致的增加量。提高它们的细胞分裂速率会增加突变,进而引发癌症。非分裂细胞几乎不会引发癌症。内源性细胞分裂速率可受激素水平影响,热量限制会使其降低,而高剂量化学物质会使其升高。如果DNA损伤速率和细胞分裂速率都增加,那么对诱变作用(以及致癌作用)将产生倍增效应,例如,高剂量的诱变剂通过细胞杀伤作用增加有丝分裂时就是如此。针对活性亲电诱变剂的防御系统,如谷胱甘肽转移酶,几乎都是可诱导的,可保护细胞免受能导致DNA损伤的化学物质活性形式增加的影响。多种DNA修复防御系统,几乎都是可诱导的,可保护细胞免受DNA损伤的任何增加。因此,特定化学损伤的影响取决于每种防御的水平,而这又取决于过去的接触史。外源性物质可影响这些防御的诱导和有效性。饮食中缺乏特定的微量营养素(如抗氧化剂)可使防御功能部分丧失。