Environmental Health Science and Research Bureau, Health Canada, Ottawa, ON, Canada.
Department of Biology, Carleton University, Ottawa, ON, Canada.
Arch Toxicol. 2021 May;95(5):1631-1645. doi: 10.1007/s00204-021-03014-2. Epub 2021 Mar 26.
Transcriptomic biomarkers can be used to inform molecular initiating and key events involved in a toxicant's mode of action. To address the limited approaches available for identifying epigenotoxicants, we developed and assessed a transcriptomic biomarker of histone deacetylase inhibition (HDACi). First, we assembled a set of ten prototypical HDACi and ten non-HDACi reference compounds. Concentration-response experiments were performed for each chemical to collect TK6 human lymphoblastoid cell samples after 4 h of exposure and to assess cell viability following a 20-h recovery period in fresh media. One concentration was selected for each chemical for whole transcriptome profiling and transcriptomic signature derivation, based on cell viability at the 24-h time point and on maximal induction of HDACi-response genes (RGL1, NEU1, GPR183) or cellular stress-response genes (ATF3, CDKN1A, GADD45A) analyzed by TaqMan qPCR assays after 4 h of exposure. Whole transcriptomes were profiled after 4 h exposures by Templated Oligo-Sequencing (TempO-Seq). By applying the nearest shrunken centroid (NSC) method to the whole transcriptome profiles of the reference compounds, we derived an 81-gene toxicogenomic (TGx) signature, referred to as TGx-HDACi, that classified all 20 reference compounds correctly using NSC classification and the Running Fisher test. An additional 4 HDACi and 7 non-HDACi were profiled and analyzed using TGx-HDACi to further assess classification performance; the biomarker accurately classified all 11 compounds, including 3 non-HDACi epigenotoxicants, suggesting a promising specificity toward HDACi. The availability of TGx-HDACi increases the diversity of tools that can facilitate mode of action analysis of toxicants using gene expression profiling.
转录组生物标志物可用于提供毒物作用模式中涉及的分子起始和关键事件的信息。为了解决鉴定表观遗传毒物的方法有限的问题,我们开发并评估了一种组蛋白去乙酰化酶抑制剂 (HDACi) 的转录组生物标志物。首先,我们汇集了一组十种原型 HDACi 和十种非 HDACi 参比化合物。对每种化学物质进行浓度-反应实验,在暴露 4 小时后收集 TK6 人淋巴母细胞样品,并在新鲜培养基中恢复 20 小时后评估细胞活力。根据 24 小时时间点的细胞活力以及通过 TaqMan qPCR 分析在 4 小时暴露后最大诱导的 HDACi 反应基因 (RGL1、NEU1、GPR183) 或细胞应激反应基因 (ATF3、CDKN1A、GADD45A),选择每种化学物质的一个浓度进行全转录组谱分析和转录组特征推导。在 4 小时暴露后,通过模板寡核苷酸测序 (TempO-Seq) 进行全转录组谱分析。通过将参比化合物的全转录组谱应用于最近收缩质心 (NSC) 方法,我们得出了一个 81 个基因毒理基因组学 (TGx) 特征,称为 TGx-HDACi,该特征使用 NSC 分类和运行 Fisher 检验正确分类了所有 20 个参比化合物。另外还对 4 种 HDACi 和 7 种非 HDACi 进行了 TGx-HDACi 谱分析和分析,以进一步评估分类性能;该生物标志物准确地分类了所有 11 种化合物,包括 3 种非 HDACi 表观遗传毒物,这表明对 HDACi 具有有希望的特异性。TGx-HDACi 的可用性增加了可用于使用基因表达谱分析毒物作用模式的工具的多样性。