Division of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon 22012, Korea.
Institute for New Drug Development, Incheon National University, Incheon 22012, Korea.
Int J Mol Sci. 2020 Jul 29;21(15):5387. doi: 10.3390/ijms21155387.
An in vitro cell transformation assay (CTA) is useful for the detection of non-genotoxic carcinogens (NGTXCs); however, it does not provide information on their modes of action. In this study, to pursue a mechanism-based approach in the risk assessment of NGTXCs, we aimed to develop an integrated strategy comprising an in vitro Bhas 42 CTA and global DNA methylation analysis. For this purpose, 10 NGTXCs, which were also predicted to be negative through Derek/Sarah structure-activity relationship analysis, were first tested for transforming activity in Bhas 42 cells. Methylation profiles using reduced representation bisulfite sequencing were generated for seven NGTXCs that were positive in CTAs. In general, the differentially methylated regions (DMRs) within promoter regions showed slightly more bias toward hypermethylation than the DMRs across the whole genome. We also identified 13 genes associated with overlapping DMRs within the promoter regions in four NGTXCs, of which seven were hypermethylated and six were hypomethylated. Using ingenuity pathway analysis, the genes with DMRs at the CpG sites were found to be enriched in cancer-related categories, including "cell-to-cell signaling and interaction" as well as "cell death and survival". Moreover, the networks related to "cell death and survival", which were considered to be associated with carcinogenesis, were identified in six NGTXCs. These results suggest that epigenetic changes supporting cell transformation processes occur during non-genotoxic carcinogenesis. Taken together, our combined system can become an attractive component for an integrated approach for the testing and assessment of NGTXCs.
体外细胞转化检测(CTA)可用于检测非遗传毒性致癌物质(NGTXCs);然而,它不能提供其作用模式的信息。在这项研究中,为了在 NGTXCs 的风险评估中采用基于机制的方法,我们旨在开发一种包含体外 Bhas 42 CTA 和全基因组 DNA 甲基化分析的综合策略。为此,首先在 Bhas 42 细胞中测试了 10 种 NGTXCs 的转化活性,这些物质也通过 Derek/Sarah 结构-活性关系分析预测为阴性。对于 CTA 阳性的七种 NGTXCs,使用简化代表性亚硫酸氢盐测序生成了甲基化图谱。一般来说,启动子区域内的差异甲基化区域(DMR)比全基因组范围内的 DMR 更倾向于过度甲基化。我们还在四个 NGTXCs 中鉴定了与启动子区域内重叠 DMR 相关的 13 个基因,其中 7 个基因高甲基化,6 个基因低甲基化。使用 Ingenuity 通路分析,发现 CpG 位点有 DMR 的基因在癌症相关类别中富集,包括“细胞间信号转导和相互作用”以及“细胞死亡和存活”。此外,在六个 NGTXCs 中鉴定到与“细胞死亡和存活”相关的网络,这些网络被认为与致癌作用有关。这些结果表明,在非遗传毒性致癌作用过程中发生了支持细胞转化过程的表观遗传变化。总之,我们的联合系统可以成为测试和评估 NGTXCs 的综合方法的一个有吸引力的组成部分。