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Cell Proliferation and Formaldehyde‐Induced Respiratory Carcinogenesis

机译:细胞增殖和甲醛诱导的呼吸系统致癌

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Formaldehyde is a nasal carcinogen in the rat but the cancer risk this chemical poses for humans remains to be determined. Formaldehyde induces nonlinear, concentration‐dependent increases in nasal epithelial cell proliferation and DNA‐protein cross‐link formation following short‐term exposure. Presented in this review are results from a mechanistically based formaldehyde inhalation study in which an important endpoint was the measurement of cell proliferation indices in target sites for nasal tumor induction. Male Fischer 344 rats were exposed to 0, 0.7, 2, 6, 10, or 15 ppm formaldehyde for up to 2 years (6 hr/day, 5 day/week). Statistically significant increases in cell proliferation were confined to the 10 and 15 ppm groups, which remained elevated throughout the study. The concentration‐dependent increases in cell proliferation correlated strongly with the tumor response curve, supporting the proposal that sustained increases in cell proliferation are an important component of formaldehyde carcinogenesis. The nonlinearity observed in formaldehyde‐induced rodent nasal cancer is consistent with a high‐concentration effect of regenerative cell proliferation of the target organ coupled with the genotoxic effects of formaldehyde. Cell kinetic data from these studies provide important information that may be utilized in the assessment of risk for humans exposed to
机译:甲醛是大鼠的鼻癌物,但这种化学物质对人类构成的癌症风险仍有待确定。甲醛在短期暴露后诱导鼻上皮细胞增殖和 DNA-蛋白质交联形成的非线性、浓度依赖性增加。本综述中介绍的是一项基于机制的甲醛吸入研究的结果,其中的一个重要终点是测量鼻肿瘤诱导靶位点的细胞增殖指数。雄性Fischer 344大鼠暴露于0、0.7、2、6、10或15 ppm甲醛长达2年(6小时/天,5天/周)。细胞增殖的统计学显着增加仅限于 10 和 15 ppm 组,在整个研究过程中保持升高。细胞增殖的浓度依赖性增加与肿瘤反应曲线密切相关,支持细胞增殖持续增加是甲醛致癌的重要组成部分。在甲醛诱导的啮齿动物鼻癌中观察到的非线性与靶器官再生细胞增殖的高浓度效应以及甲醛的遗传毒性作用一致。这些研究的细胞动力学数据提供了重要信息,可用于评估暴露于以下人群的风险

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