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致癌物关键特征在癌症危害识别中的应用。

Application of the key characteristics of carcinogens in cancer hazard identification.

机构信息

Monographs Programme, International Agency for Research on Cancer, Lyon, France.

Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, TX, USA.

出版信息

Carcinogenesis. 2018 Apr 5;39(4):614-622. doi: 10.1093/carcin/bgy031.

Abstract

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.

摘要

史密斯等人(《环境卫生展望》124:713, 2016)确定了 10 个关键特征(KC),其中一个或多个特征通常存在于已确立的人类致癌物中。这些 KC 反映了致癌剂的特性,例如“是否具有遗传毒性”、“是否具有免疫抑制作用”或“是否调节受体介导的效应”,与癌症的特征不同,后者是肿瘤的特性。为了评估将 KC 应用于不同物质的可行性和局限性,从最近的 8 次 IARC 专论会议中汇编了机制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广泛的文献,涵盖了这些会议中确定的大多数(12/16)IARC 第 1 组或 2A 类致癌物的多个 KC。其中 5 种致癌物质具有遗传毒性并诱导氧化应激,其中五氯苯酚、联氨和马拉硫磷还表现出其他 KC。其他 4 种致癌物质,包括焊接烟尘,具有免疫抑制作用。仅根据两种物质(四溴双酚 A 和四氯偶氮苯)的机制数据,将总体评估升级为 2A 组。这两种致癌物质与其他 KC 一起调节受体介导的效应。对 2B 组或 3 组物质的研究较少,其中绝大多数(17/18)仅表现出一个或没有 KC。因此,一种识别和评估与癌症相关的机制研究的客观方法为大多数第 1 组或 2A 类致癌物提供了多个 KC 的有力证据,但也确定了改进的机会。进一步开发和映射与 KC 相关的毒性和生物标志物终点和途径,可以促进系统地搜索和评估致癌危害识别中的机制数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/941d/5888955/ec36117ea26b/bgy03101.jpg

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