Munro I C
Canadian Centre for Toxicology, Guelph, Ontario.
Biomed Environ Sci. 1988 Jun;1(1):51-8.
Regulatory agencies and public health authorities make extensive use of laboratory data on chemical carcinogenicity in the establishment of acceptable human exposure standards. Risk assessment practices require the quantitative extrapolation of animal data to the human setting. In this paper, the scientific assumptions underlying risk assessment are evaluated and future research needs are identified. Consideration also is given to the role of promotion assays in the evaluation of carcinogenesis and the part played by short-term tests for carcinogenicity in the regulatory process.
监管机构和公共卫生当局在制定可接受的人体接触标准时,广泛使用有关化学致癌性的实验室数据。风险评估实践要求将动物数据定量外推至人体情况。本文评估了风险评估背后的科学假设,并确定了未来的研究需求。同时还考虑了促癌试验在致癌作用评估中的作用以及短期致癌性试验在监管过程中所起的作用。