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利用啮齿动物致癌性试验结果来确定对人类的潜在癌症风险。

Use of rodent carcinogenicity test results for determining potential cancer risk to humans.

作者信息

Infante P F

机构信息

Health Standards Program, Occupational Safety & Health Administration, Washington, DC 20210.

出版信息

Environ Health Perspect. 1993 Dec;101 Suppl 5(Suppl 5):143-8. doi: 10.1289/ehp.93101s5143.

Abstract

A high proportion of "human" and "probable human" carcinogens as categorized by the International Agency for Research on Cancer have been identified through observations in workers. The excess cancer risk has often been quite high. Most substances known to cause cancer in humans are now known to cause cancer in animals. In the past two decades, an increasing number of substances first shown to cause cancer in animals are now known to cause or are highly suspected of causing cancer in humans (and quite often in workers). The observations necessitate the use of rodent cancer test results for identifying and regulating potential environmental carcinogens. The role of cell proliferation (CP) in the carcinogenic response is important from a regulatory view in terms of both qualitative and quantitative evidence. If CP influences the carcinogenic response, the use of such data to modify dose response in the low-dose range is another factor that needs to be considered. Presentations at this symposium, however, indicate that CP data at the present time should not be incorporated into cancer risk assessments. More simple concepts that affect quantitative dose response and that may result in an artificially low estimated risk but could be adjusted for in the bioassay protocol have usually been ignored. A balanced approach would be to incorporate all known factors that influence quantitative estimates of cancer risk when conducting animal cancer bioassays and extrapolating those results to humans.

摘要

国际癌症研究机构分类的“人类”和“可能的人类”致癌物中,很大一部分是通过对工人的观察确定的。额外的癌症风险往往相当高。现在已知大多数在人类中致癌的物质在动物中也会致癌。在过去二十年中,越来越多最初在动物中显示致癌的物质现在已知会导致或高度怀疑会导致人类(而且通常是工人)患癌。这些观察结果使得有必要利用啮齿动物癌症试验结果来识别和监管潜在的环境致癌物。从定性和定量证据的监管角度来看,细胞增殖(CP)在致癌反应中的作用很重要。如果CP影响致癌反应,那么利用此类数据在低剂量范围内修改剂量反应是另一个需要考虑的因素。然而,本次研讨会的报告表明,目前CP数据不应纳入癌症风险评估。影响定量剂量反应且可能导致人为低估风险但可在生物测定方案中进行调整的更简单概念通常被忽视。一种平衡的方法是在进行动物癌症生物测定并将结果外推至人类时,纳入所有已知影响癌症风险定量估计的因素。

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