Portier C J, Bailer A J
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
J Toxicol Environ Health. 1989;27(1):21-45. doi: 10.1080/15287398909531276.
The tumor incidence rate is modeled for various tumors in a database of control animals [Fischer 344 rats and (C57BL/6 x C3H)F1 mice] originally developed by the national Toxicology Program and recently augmented to include additional sacrifice data by Portier et al. (1986). These rates are assumed to follow a clonal two-stage model of carcinogenesis where cells in the various tissues are allowed to be in one of three states arbitrarily defined as a "normal" state, an "initiated" state, and a "tumor present" state. The parameters of this clonal two-stage model have a direct interpretation with regard to the mechanism of action and in some cases may suggest a common mechanism for various tumors in the different sex/species groups. Also, the risk of dying (from all causes) in tumor-bearing animals is compared to the risk of dying in non-tumor-bearing animals via estimates of relative risk. In general, it was found that the risk of dying was elevated for most tumors. The purpose of this analysis is to provide estimates of baseline tumor rates and relative risks, which are useful in the design and analysis of future carcinogenicity experiments.
肿瘤发生率是根据一个对照动物数据库(国家毒理学计划最初建立的费希尔344大鼠和(C57BL/6xC3H)F1小鼠)中各种肿瘤的情况进行建模的,该数据库最近由波捷等人(1986年)补充了额外的处死数据。这些发生率假定遵循克隆性两阶段致癌模型,其中各种组织中的细胞可以处于三种状态之一,这三种状态被任意定义为“正常”状态、“启动”状态和“有肿瘤”状态。这种克隆性两阶段模型的参数对作用机制有直接解释,在某些情况下可能暗示不同性别/物种组中各种肿瘤的共同机制。此外,通过相对风险估计,将患肿瘤动物的死亡风险(各种原因导致的)与未患肿瘤动物的死亡风险进行比较。一般来说,发现大多数肿瘤的死亡风险有所升高。该分析的目的是提供基线肿瘤发生率和相对风险的估计值,这在未来致癌性实验的设计和分析中很有用。