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致癌作用的一般概率模型:实验性膀胱癌分析

A general probabilistic model of carcinogenesis: analysis of experimental urinary bladder cancer.

作者信息

Greenfield R E, Ellwein L B, Cohen S M

出版信息

Carcinogenesis. 1984 Apr;5(4):437-45. doi: 10.1093/carcin/5.4.437.

Abstract

A theoretical model of two-stage carcinogenesis has been hypothesized. Variables that are modeled include the populations of normal, initiated, and transformed cells; mitotic rates of these cells; hyperplasia; and the probabilities of cell initiation and transformation during replication. The size of the cell populations can be estimated and mitotic rates determined directly from animal studies. Tumor occurrences at different time intervals following varying periods of N-[4-(5-nitro-2-furyl)-2-thiazolyl]formamide (FANFT) and sodium saccharin administration are known and are used in the indirect estimation of values for unobservable model variables. Model-based analyses suggest FANFT markedly increases the probability of cell initiation in addition to its experimentally verifiable effects on increasing the stem cell population and mitotic rates. Further, experimental results appear inconsistent with the hypothesis that FANFT increases the probability of cell transformation over background levels. Similarly, the effect of sodium saccharin was found to be attributable entirely to increases in stem cell populations and mitotic rates without influencing either the probability of initiation or the probability of transformation.

摘要

已经提出了一个两阶段致癌作用的理论模型。被建模的变量包括正常细胞、启动细胞和转化细胞的群体;这些细胞的有丝分裂率;细胞增生;以及复制过程中细胞启动和转化的概率。细胞群体的大小可以从动物研究中直接估计出来,有丝分裂率也可以直接确定。已知在给予不同时期的N-[4-(5-硝基-2-呋喃基)-2-噻唑基]甲酰胺(FANFT)和糖精钠后不同时间间隔的肿瘤发生率,并用于间接估计不可观察的模型变量的值。基于模型的分析表明,FANFT除了对增加干细胞群体和有丝分裂率有实验可验证的作用外,还显著增加了细胞启动的概率。此外,实验结果似乎与FANFT增加细胞转化概率超过背景水平的假设不一致。同样,发现糖精钠的作用完全归因于干细胞群体和有丝分裂率的增加,而不影响启动概率或转化概率。

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