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Correlation of In  Vivo Versus In Vitro Benchmark Doses (BMDs) Derived From Micronucleus Test Data: A Proof of Concept Study

机译:从微核试验数据得出的体内与体外基准剂量(BMD)的相关性:概念研究的证明

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摘要

In this study, we explored the applicability of using in vitro micronucleus (MN) data from human lymphoblastoid TK6 cells to derive in vivo genotoxicity potency information. Nineteen chemicals covering a broad spectrum of genotoxic modes of action were tested in an in vitro MN test using TK6 cells using the same study protocol. Several of these chemicals were considered to need metabolic activation, and these were administered in the presence of S9. The Benchmark dose (BMD) approach was applied using the dose-response modeling program PROAST to estimate the genotoxic potency from the in vitro data. The resulting in vitro BMDs were compared with previously derived BMDs from in vivo MN and carcinogenicity studies. A proportional correlation was observed between the BMDs from the in vitro MN and the BMDs from the in vivo MN assays. Further, a clear correlation was found between the BMDs from in vitro MN and the associated BMDs for malignant tumors. Although these results are based on only 19 compounds, they show that genotoxicity potencies estimated from in vitro tests may result in useful information regarding in vivo genotoxic potency, as well as expected cancer potency. Extension of the number of compounds and further investigation of metabolic activation (S9) and of other toxicokinetic factors would be needed to validate our initial conclusions. However, this initial work suggests that this approach could be used for in vitro to in vivo extrapolations which would support the reduction of animals used in research (3Rs: replacement, reduction, and refinement).
机译:在这项研究中,我们探索了使用来自人类淋巴母细胞TK6细胞的体外微核(MN)数据得出体内遗传毒性效能信息的适用性。使用TK6细胞在体外MN试验中使用相同的研究方案对涵盖广泛的遗传毒性作用模式的19种化学物质进行了测试。这些化学物质中有几种被认为需要代谢激活,这些化学物质在S9存在的情况下给药。使用剂量响应建模程序PROAST应用了基准剂量(BMD)方法,以根据体外数据估算遗传毒性潜力。将所得的体外BMD与先前来自体内MN和致癌性研究的BMD进行比较。观察到来自体外MN的BMD与来自体内MN测定的BMD之间成比例的相关性。此外,在来自体外MN的BMD与恶性肿瘤的相关BMD之间发现了明显的相关性。尽管这些结果仅基于19种化合物,但它们表明从体外试验估计的遗传毒性潜力可能会提供有关体内遗传毒性潜力以及预期的癌症效力的有用信息。为了证实我们的初步结论,需要扩展化合物的数量并进一步研究代谢活化(S9)和其他毒代动力学因子。但是,这项初步工作表明该方法可用于体外至体内外推法,这将有助于减少研究中使用的动物数量(3R:替代,减少和改良)。

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