Interaction between two carcinogens in the two-stage clonal expansion model of carcinogenesis.

J. Zielinski, R. Kodell, D. Krewski
{"title":"Interaction between two carcinogens in the two-stage clonal expansion model of carcinogenesis.","authors":"J. Zielinski, R. Kodell, D. Krewski","doi":"10.1080/135952201753172999","DOIUrl":null,"url":null,"abstract":"BACKGROUND Exposure to two or more carcinogens may result in interactive effects in which the joint effect may be greater or less than that expected to arise as the sum of the effects of the two agents alone. In this article, we investigate the joint effects of exposure to two carcinogens within the context of the two-stage clonal expansion model of carcinogenesis. METHODS Different measures of interaction are considered based on the notions of response and dose additivity, and an index of synergy S due to Thomas (1982) used to broadly characterise the effects of joint exposure. RESULTS Interactive effects based on the index S were found to be qualitatively similar, regardless of whether cancer risk was defined in terms of age-specific relative risk, or the cumulative probability of cancer occurrence at the same age. For joint exposure to two initiators or to two completers (affecting the first or second mutation rate in the two-mutation model, respectively), S assumed values near zero, reflecting an additive relative-risk relationship. For joint exposure to two promoters (which increase the rate of proliferation of initiated cells that have sustained the first mutation), the relative-risk relationship was found to range from supramultiplicative (S > 1) in younger age groups, to subadditive (S < 0) in older ages. Other combinations of carcinogens involving promotion also displayed a broad range of interaction effects. CONCLUSIONS These results differ markedly from those reported previously by Kodell et al. (1991) for an approximate form of the two-stage model, which predicts much higher values of the index of synergy S than the exact form of the model when promotion is involved.","PeriodicalId":80024,"journal":{"name":"Journal of epidemiology and biostatistics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of epidemiology and biostatistics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/135952201753172999","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8

Abstract

BACKGROUND Exposure to two or more carcinogens may result in interactive effects in which the joint effect may be greater or less than that expected to arise as the sum of the effects of the two agents alone. In this article, we investigate the joint effects of exposure to two carcinogens within the context of the two-stage clonal expansion model of carcinogenesis. METHODS Different measures of interaction are considered based on the notions of response and dose additivity, and an index of synergy S due to Thomas (1982) used to broadly characterise the effects of joint exposure. RESULTS Interactive effects based on the index S were found to be qualitatively similar, regardless of whether cancer risk was defined in terms of age-specific relative risk, or the cumulative probability of cancer occurrence at the same age. For joint exposure to two initiators or to two completers (affecting the first or second mutation rate in the two-mutation model, respectively), S assumed values near zero, reflecting an additive relative-risk relationship. For joint exposure to two promoters (which increase the rate of proliferation of initiated cells that have sustained the first mutation), the relative-risk relationship was found to range from supramultiplicative (S > 1) in younger age groups, to subadditive (S < 0) in older ages. Other combinations of carcinogens involving promotion also displayed a broad range of interaction effects. CONCLUSIONS These results differ markedly from those reported previously by Kodell et al. (1991) for an approximate form of the two-stage model, which predicts much higher values of the index of synergy S than the exact form of the model when promotion is involved.
两种致癌物在两期克隆扩增模型中的相互作用。
接触两种或两种以上致癌物可能产生相互作用,其中联合作用可能大于或小于两种致癌物单独作用的总和。在本文中,我们在致癌的两阶段克隆扩展模型的背景下研究暴露于两种致癌物质的联合效应。方法根据反应和剂量可加性的概念考虑不同的相互作用度量,并使用Thomas(1982)的协同效应指数S来广泛表征联合暴露的影响。结果:无论癌症风险是根据特定年龄的相对风险来定义,还是根据同一年龄癌症发生的累积概率来定义,基于指数S的交互效应在质量上是相似的。对于联合暴露于两个启动者或两个完成者(分别影响双突变模型中的第一或第二突变率),S假设值接近于零,反映了一种可加性相对风险关系。对于联合暴露于两种启动子(这增加了维持第一次突变的起始细胞的增殖速度),发现相对风险关系的范围从年轻年龄组的超增殖(S < 0)到老年组的亚加性(S < 0)。致癌物质的其他组合也表现出广泛的相互作用。这些结果与之前由Kodell等人(1991)报道的两阶段模型的近似形式有明显不同,当涉及促销时,两阶段模型预测的协同指数S值要比模型的精确形式高得多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信