Gold L S, Ward J M, Bernstein L, Stern B
Fundam Appl Toxicol. 1986 May;6(4):677-90. doi: 10.1016/0272-0590(86)90181-8.
Carcinogenic potency (TD50) estimated from the results of 88 NCI/NTP carcinogenesis bioassays was examined by common target sites in rats and mice. Other indicators of a chemical's hazard were investigated, including whether tumors were induced at more than one site in a single sex-species group of test animals, whether tumors may have caused the death of the animal or were found at sacrifice, and whether metastases of induced tumors occurred. These hazard indicators are sometimes interrelated; however, the potency (TD50) values of chemicals which are hazardous by each of these measures spanned a wide range. Carcinogens which caused some type of fatal tumor were more likely than other carcinogens to cause tumors in multiple organ sites and multiple sex-species groups. Since these other hazard indicators were not related to carcinogenic potency, they should be included along with potency estimates such as the TD50 in summarizing the potential dangers of human exposures to a carcinogen and in comparisons of hazard among carcinogens.
根据88项美国国立癌症研究所/国家毒理学计划致癌生物测定结果估算的致癌效力(半数致癌剂量),通过大鼠和小鼠的常见靶位点进行了研究。还调查了化学物质危害的其他指标,包括在单一性别-物种组的试验动物中是否在多个部位诱发肿瘤、肿瘤是否可能导致动物死亡或在处死后发现,以及诱发肿瘤是否发生转移。这些危害指标有时相互关联;然而,通过这些措施中的每一项判定为有害的化学物质的效力(半数致癌剂量)值范围很广。导致某种致命肿瘤的致癌物比其他致癌物更有可能在多个器官部位和多个性别-物种组中诱发肿瘤。由于这些其他危害指标与致癌效力无关,因此在总结人类接触致癌物的潜在危险以及比较致癌物之间的危害时,应将它们与诸如半数致癌剂量之类的效力估计值一起纳入。