Krewski D, Gaylor D W, Soms A P, Szyszkowicz M
Health Protection Branch, Health and Welfare Canada Ottawa, Ontario, Canada.
Risk Anal. 1993 Aug;13(4):383-98. doi: 10.1111/j.1539-6924.1993.tb00738.x.
Current practice in carcinogen bioassay calls for exposure of experimental animals at doses up to and including the maximum tolerated dose (MTD). Such studies have been used to compute measures of carcinogenic potency such as the TD50 as well as unit risk factors such as q1 * for predicting low-dose risks. Recent studies have indicated that these measures of carcinogenic potency are highly correlated with the MTD. Carcinogenic potency has also been shown to be correlated with indicators of mutagenicity and toxicity. Correlation of the MTDs for rats and mice implies a corresponding correlation in TD50 values for these two species. The implications of these results for cancer risk assessment are examined in light of the large variation in potency among chemicals known to induce tumors in rodents.
目前致癌物生物测定的做法要求以高达并包括最大耐受剂量(MTD)的剂量对实验动物进行暴露。此类研究已被用于计算致癌效力的指标,如TD50,以及单位风险因子,如q1*,以预测低剂量风险。最近的研究表明,这些致癌效力指标与MTD高度相关。致癌效力也已被证明与致突变性和毒性指标相关。大鼠和小鼠MTD之间的相关性意味着这两个物种的TD50值也存在相应的相关性。鉴于已知在啮齿动物中诱发肿瘤的化学物质之间效力差异很大,本文将探讨这些结果对癌症风险评估的影响。