Nestmann E R, Bryant D W, Carr C J
CanTox Inc., Mississauga, Ontario, Canada.
Regul Toxicol Pharmacol. 1996 Aug;24(1 Pt 1):9-18. doi: 10.1006/rtph.1996.0059.
A workshop was held to discuss the uses of data on DNA adduct measurement in humans and in experimental systems in vitro and in vivo. The discussions focused principally on the understanding of the toxicological significance of DNA adducts as provided by information from animal models. An Expert Panel concluded that human DNA adduct data have utility in several aspects of risk assessment. The presence and amount of specific adducts that can be correlated with a chemical exposure are relevant for hazard identification and risk evaluation. Data from experimental systems have established dose-response relationships between the level of adducts and exposure, but these remain complex and depend on metabolic fate. Although structure-activity relationships have been useful retrospectively to explain the DNA-reactive nature of some chemicals or classes of chemicals, there are currently no means outside the laboratory to specifically predict the adduct-producing potency of a compound. Analysis of DNA adducts in tissues of laboratory animals and humans has revealed sensitive subpopulations, a finding that has important relevance for human risk assessment. Adduct analysis may be one of the best tools available to characterize exposures to DNA from complex mixtures for purposes of epidemiological investigation. Consensus statements were developed based on presentations by R. Gupta, W. Lutz, R. Nath, and B. Singer [see Regul. Toxicol. Pharmacol. 23(1), 1996] and subsequent discussions. First, rigorous scientific criteria should be met for the detection and characterization of specific DNA adducts in vitro and in target tissues in vivo. Second, the use of adduct data in risk extrapolation has the greatest value when there is characterization of adduct structure, an understanding of the role of repair in DNA adduct removal, and demonstration of biological relevance for each adduct. Third, the detection of DNA adducts in a tissue does not necessarily indicate a specific tumorigenic risk for that tissue. Fourth, the mutagenic potency for specific adducts varies by several orders of magnitude. Fifth, the role of DNA adducts induced by exogenous agents must be placed in perspective of endogenously produced adducts. The biological significance of a type of DNA adduct is related to several factors, including the efficiency of conversion to mutation, the amounts of similar endogenous adducts, and the variety of exogenous DNA adducts found in DNA from humans. The biological relevance of DNA adducts may be deduced from the dose-response relationships for adducts and tumors at physiologically relevant doses as well as from data showing mutations in targets such as oncogenes or tumor suppressor genes. There is convincing evidence in the literature for an association between some specific DNA adducts, mutation, and the carcinogenic process. As a general conclusion, the Panel suggested that the current technological capabilities for detection of DNA adducts exceed our ability to define the biological significance of adducts as it relates to toxicity or health outcome. DNA adducts are likely to play an important role in human risk for cancer induction and progression, but the quantitative aspects of this relationship remain to be determined.
举办了一次研讨会,讨论人类以及体外和体内实验系统中DNA加合物测量数据的用途。讨论主要集中在理解动物模型提供的信息所显示的DNA加合物的毒理学意义。一个专家小组得出结论,人类DNA加合物数据在风险评估的几个方面具有实用价值。可与化学物暴露相关联的特定加合物的存在和数量与危害识别和风险评估相关。实验系统的数据已确立了加合物水平与暴露之间的剂量-反应关系,但这些关系仍然很复杂,并且取决于代谢命运。尽管结构-活性关系在回顾性地解释某些化学物或化学物类别与DNA反应的性质方面很有用,但目前在实验室之外尚无手段可具体预测一种化合物产生加合物的能力。对实验动物和人类组织中的DNA加合物分析已揭示出敏感亚群,这一发现对人类风险评估具有重要意义。加合物分析可能是可用于在流行病学调查中表征复杂混合物中DNA暴露情况的最佳工具之一。基于R. Gupta、W. Lutz、R. Nath和B. Singer的报告[见《Regul. Toxicol. Pharmacol.》23(1),1996]以及随后的讨论形成了共识声明。第一,在体外和体内靶组织中检测和表征特定DNA加合物应符合严格的科学标准。第二,当对加合物结构进行表征、理解修复在去除DNA加合物中的作用并证明每种加合物的生物学相关性时,在风险外推中使用加合物数据具有最大价值。第三,在一个组织中检测到DNA加合物并不一定表明该组织存在特定的致癌风险。第四,特定加合物的致突变能力相差几个数量级。第五,必须从内源性产生的加合物的角度看待外源性物质诱导的DNA加合物的作用。一种DNA加合物的生物学意义与几个因素有关,包括转化为突变的效率、类似内源性加合物的数量以及在人类DNA中发现的外源性DNA加合物的种类。DNA加合物的生物学相关性可从生理相关剂量下加合物与肿瘤的剂量-反应关系以及显示癌基因或肿瘤抑制基因等靶标发生突变的数据中推导出来。文献中有令人信服的证据表明某些特定DNA加合物、突变与致癌过程之间存在关联。作为一个总体结论,该小组建议,目前检测DNA加合物的技术能力超过了我们界定加合物与毒性或健康结果相关的生物学意义的能力。DNA加合物可能在人类癌症诱发和进展风险中起重要作用,但这种关系的定量方面仍有待确定。