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How well can carcinogenicity be predicted by high throughput “characteristics of carcinogens” mechanistic data?

机译:通过高通量的“致癌物体”机械数据来预测致癌性的程度如何?

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Abstract IARC has begun using ToxCast/Tox21 data in efforts to represent key characteristics of carcinogens to organize and weigh mechanistic evidence in cancer hazard determinations and this implicit inference approach also is being considered by USEPA. To determine how well ToxCast/Tox21 data can explicitly predict cancer hazard, this approach was evaluated with statistical analyses and machine learning prediction algorithms. Substances USEPA previously classified as having cancer hazard potential were designated as positives and substances not posing a carcinogenic hazard were designated as negatives. Then ToxCast/Tox21 data were analyzed both with and without adjusting for the cytotoxicity burst effect commonly observed in such assays. Using the same assignments as IARC of ToxCast/Tox21 assays to the seven key characteristics of carcinogens, the ability to predict cancer hazard for each key characteristic, alone or in combination, was found to be no better than chance. Hence, we have little scientific confidence in IARC's inference models derived from current ToxCast/Tox21 assays for key characteristics to predict cancer. This finding supports the need for a more rigorous mode-of-action pathway-based framework to organize, evaluate, and integrate mechanistic evidence with animal toxicity, epidemiological investigations, and knowledge of exposure and dosimetry to evaluate potential carcinogenic hazards and risks to humans. Highlights ? IARC's use of ToxCast/Tox21 HTS data has followed implied/unverified inference. ? Hence, we explicitly tested how well such HTS data predict cancer classifications. ? HTS data for EPA classified carcinogens were fit to 7 IARC key characteristics (KC). ? Statistics & machine learning algorithms were used to analyze predictions of cancer. ? Results: HTS 7?KC data were no better than chance alone in predicting cancer.
机译:摘要IARC已经开始使用Toxcast / TOX21数据在努力中代表致癌和称重机械证据的关键特征,在癌症危害确定中,这种隐式推断方法也被使用PA考虑。为了确定ToxCast / TOX21数据如何明确预测癌症危害,通过统计分析和机器学习预测算法评估这种方法。先前分类为具有癌症危害潜力的物质使用PAA被指定为未造成致癌危害的阳性和物质被指定为底片。然后在不调整在这种测定中通常观察到的细胞毒性突发效果,分析ToxCast / TOX21数据。使用与Toxcast / TOX21的IARC的同一分配给致癌的七个关键特征,发现每个关键特征,单独或组合地预测癌症危害的能力并不比机会更好。因此,我们对IARC的推理模型进行了很小的科学信心,该模型来自目前的TOXCAST / TOX21测定以预测癌症的关键特征。这一发现支持更严格的动作模式基于模式,以组织,评估和整合具有动物毒性,流行病学调查和接触和剂量测定的知识来组织,评估和整合机制证据,以评估潜在的致癌危害和对人类的风险。强调 ? IARC使用Toxcast / Tox21 HTS数据遵循默示/未经验证的推断。还因此,我们明确测试了这种HTS数据如何预测癌症分类。还EPA分类致癌物质的HTS数据适用于7个IARC关键特征(KC)。还统计和机器学习算法用于分析癌症的预测。还结果:HTS 7?KC数据不比单独预测癌症的机会更好。

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