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Application of the key characteristics of carcinogens in cancer hazard identification

机译:致癌物关键特性在癌症危险性识别中的应用

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摘要

Smith et al. (Env. Health Perspect. 124: 713, 2016) identified 10 key characteristics (KCs), one or more of which are commonly exhibited by established human carcinogens. The KCs reflect the properties of a cancer-causing agent, such as ‘is genotoxic,’ ‘is immunosuppressive’ or ‘modulates receptor-mediated effects,’ and are distinct from the hallmarks of cancer, which are the properties of tumors. To assess feasibility and limitations of applying the KCs to diverse agents, methods and results of mechanistic data evaluations were compiled from eight recent IARC Monograph meetings. A systematic search, screening and evaluation procedure identified a broad literature encompassing multiple KCs for most (12/16) IARC Group 1 or 2A carcinogens identified in these meetings. Five carcinogens are genotoxic and induce oxidative stress, of which pentachlorophenol, hydrazine and malathion also showed additional KCs. Four others, including welding fumes, are immunosuppressive. The overall evaluation was upgraded to Group 2A based on mechanistic data for only two agents, tetrabromobisphenol A and tetrachloroazobenzene. Both carcinogens modulate receptor-mediated effects in combination with other KCs. Fewer studies were identified for Group 2B or 3 agents, with the vast majority (17/18) showing only one or no KCs. Thus, an objective approach to identify and evaluate mechanistic studies pertinent to cancer revealed strong evidence for multiple KCs for most Group 1 or 2A carcinogens but also identified opportunities for improvement. Further development and mapping of toxicological and biomarker endpoints and pathways relevant to the KCs can advance the systematic search and evaluation of mechanistic data in carcinogen hazard identification.
机译:史密斯等。 (Env。Health Perspect。124:713,2016)确定了10个关键特征(KC),其中一项或多项通常由已确立的人类致癌物表现出来。 KC反映了致癌剂的性质,例如“遗传毒性”,“免疫抑制性”或“调节受体介导的作用”,并且不同于癌症的特征,后者是肿瘤的特征。为了评估将KC应用于各种代理的可行性和局限性,从最近的IARC专题会议的八次会议中收集了机械数据评估的方法和结果。系统的搜索,筛选和评估程序确定了涵盖这些会议中确定的大多数(12/16)IARC 1类或2A类致癌物的多种KC的广泛文献。五种致癌物具有遗传毒性,并引起氧化应激,其中五氯苯酚,肼和马拉硫磷也显示出额外的KC。包括焊接烟雾在内的其他四种具有免疫抑制作用。基于仅两种试剂四溴双酚A和四氯偶氮苯的机理数据,总体评估被升级为2A组。两种致癌物均与其他KCs一起调节受体介导的作用。很少有研究针对2B或3组特工,绝大多数(17/18)仅显示一个或没有KC。因此,一种鉴定和评估与癌症有关的机制研究的客观方法揭示了大多数第1或2A类致癌物具有多个KC的有力证据,但也发现了改善的机会。与KCs有关的毒理学和生物标志物终点及途径的进一步开发和作图可以促进对致癌物危险性鉴定的机理数据进行系统的搜索和评估。

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