Weisburger J H, Williams G M
Environ Health Perspect. 1983 Apr;50:233-45. doi: 10.1289/ehp.8350233.
Health risk analysis needs to apply newer developments in the understanding of the underlying mechanisms of the carcinogenic process which has allowed for the classification of chemical carcinogens into those that damage genetic material directly (genotoxic carcinogens) and those that operate by indirect or epigenetic mechanisms. We propose a systematic decision point approach for detecting and evaluating substances for carcinogenic risk. This approach recognizes that genotoxic and epigenetic agents operate by different mechanisms and distinguishes between these two categories of carcinogens primarily on the basis of results in a battery of short-term tests that includes systems which reliably detect genotoxic carcinogens and others which may respond to epigenetic agents. Genotoxic carcinogens at very low dosages may have practical, effective threshold no-effect levels, but, nevertheless, because of their mechanism of action they are regarded as a qualitative hazard. The action of epigenetic agents of the promoter class is highly dose-dependent and reversible, and thus, a distinctively different health risk analysis is required for these agents to take account of their quantitatively lesser hazard.
健康风险分析需要应用对致癌过程潜在机制理解方面的最新进展,这使得化学致癌物能够被分类为直接损害遗传物质的致癌物(遗传毒性致癌物)和通过间接或表观遗传机制起作用的致癌物。我们提出一种系统的决策点方法来检测和评估物质的致癌风险。这种方法认识到遗传毒性和表观遗传剂通过不同机制起作用,并主要根据一系列短期试验的结果区分这两类致癌物,这些试验包括能够可靠检测遗传毒性致癌物的系统和可能对表观遗传剂有反应的其他系统。极低剂量的遗传毒性致癌物可能有实际、有效的阈值无效应水平,但是,由于其作用机制,它们被视为一种定性危害。启动子类表观遗传剂的作用高度依赖剂量且是可逆的,因此,对于这些物质需要进行明显不同的健康风险分析,以考虑其在数量上较小的危害。