Sicińska Paulina, Jabłońska Ewa, Bukowska Bożena, Balcerczyk Aneta, Reszka Edyta
Department of Biophysics of Environmental Pollution, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Poland.
Department of Translational Research, Nofer Institute of Occupational Medicine, Teresy 8, 91-348 Lodz, Poland.
Toxicol In Vitro. 2022 Aug;82:105369. doi: 10.1016/j.tiv.2022.105369. Epub 2022 Apr 27.
Phthalates are classified as non-genotoxic carcinogens. These compounds do not cause direct DNA damage but may induce indirect DNA lesions leading to cancer development. In the presented paper we have studied the effect of di-n-butyl phthalate (DBP), butylbenzyl phthalate (BBP), and their metabolites, such as mono-n-butyl phthalate (MBP) and monobenzyl phthalate (MBzP) on selected epigenetic parameters in human peripheral blood mononuclear cells (PBMCs). The cells were incubated with tested phthalates at 0.001, 0.01 and 0.1 μg/mL for 24 h. Next, global DNA methylation, methylation in the promoter regions of tumor suppressor genes (P16, TP53) and proto-oncogenes (BCL2, CCND1) were assessed as well as the expression profile of the indicated genes was analysed. The obtained results have revealed significant reduction of global DNA methylation level in PBMCs exposed to BBP, MBP and MBzP. Phthalates changed methylation pattern of the tested genes, decreased expression of P16 and TP53 genes and increased the expression of BCL2 and CCND1. In conclusion, our results have shown that the examined phthalates disturbed the processes of methylation and expression of tumor suppressor genes (P16, TP53) and protooncogenes (BCL2, CCND1) in human PBMCs.
邻苯二甲酸盐被归类为非基因毒性致癌物。这些化合物不会引起直接的DNA损伤,但可能诱导间接的DNA损伤,从而导致癌症发展。在本论文中,我们研究了邻苯二甲酸二丁酯(DBP)、邻苯二甲酸丁苄酯(BBP)及其代谢产物,如单丁基邻苯二甲酸酯(MBP)和单苄基邻苯二甲酸酯(MBzP)对人外周血单核细胞(PBMCs)中选定表观遗传参数的影响。将细胞与浓度为0.001、0.01和0.1μg/mL的受试邻苯二甲酸盐孵育24小时。接下来,评估了整体DNA甲基化、肿瘤抑制基因(P16、TP53)和原癌基因(BCL2、CCND1)启动子区域的甲基化情况,并分析了上述基因的表达谱。所得结果显示,暴露于BBP、MBP和MBzP的PBMCs中整体DNA甲基化水平显著降低。邻苯二甲酸盐改变了受试基因的甲基化模式,降低了P16和TP53基因的表达,并增加了BCL2和CCND1的表达。总之,我们的结果表明,所检测的邻苯二甲酸盐扰乱了人PBMCs中肿瘤抑制基因(P16、TP53)和原癌基因(BCL2、CCND1)的甲基化和表达过程。