DeMarini D M, Lewtas J, Brockman H E
Genetic Toxicology Division, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711.
Cell Biol Toxicol. 1989 Jun;5(2):189-200. doi: 10.1007/BF00122652.
By definition, short-term tests (STTs) for genetic toxicity detect genotoxic agents, not carcinogens specifically. However, there is sufficient evidence, based on mechanistic considerations alone, to say that genotoxic agents are potential carcinogens. STTs have high statistical power, are almost always replicated, can be performed rather easily under various sets of experimental conditions, are relatively inexpensive, and detect a variety of endpoints relevant to carcinogenesis. In addition, several STTs have shown considerable utility in evaluating the genotoxic effects of real-world, environmental complex mixtures as well as the antimutagenic effects of various pure compounds and complex mixtures. STTs are likely to continue to be refined, resulting in STTs that are increasingly more relevant to human mutation and disease. Their utility should not be judged solely against the questionable standard of a rodent carcinogenicity assay.
根据定义,遗传毒性短期试验(STT)检测的是遗传毒性剂,而非特定的致癌物。然而,仅基于机制方面的考虑就有充分证据表明,遗传毒性剂是潜在的致癌物。STT具有较高的统计效力,几乎总是可重复的,能在各种实验条件下较为容易地进行,成本相对较低,并且能检测与致癌作用相关的多种终点指标。此外,几种STT在评估现实世界中的环境复杂混合物的遗传毒性效应以及各种纯化合物和复杂混合物的抗诱变效应方面已显示出相当大的实用性。STT可能会继续得到改进,从而产生与人类突变和疾病越来越相关的STT。其效用不应仅以啮齿动物致癌性试验这一有问题的标准来评判。