Department of Pharmacotherapy and Translational Research, College of Pharmacy, Center for Pharmacogenomics and Precision Medicine, University of Florida, Gainesville, FL 32610, USA.
Molecules. 2024 Nov 16;29(22):5407. doi: 10.3390/molecules29225407.
CYP3As are important drug-metabolizing enzymes in the liver. The causes for large inter-person variability in CYP3A expression/activity remain poorly understood. DNA methylation broadly regulates gene expression and the developmental transition from fetal CYP3A7 to adult CYP3A4, and CpG methylation upstream of the CYP3A4 promoter is associated with its expression. However, because non-promoter CYP3A regulatory regions remain largely uncharacterized, how DNA methylation influences CYP3A expression has yet to be fully explored. We recently identified a distal regulatory region (DRR) that controls the expression of CYP3A4, CYP3A5, and CYP3A7. Here, we investigated the relationship between CYP3A expression and the methylation status of 16 CpG sites within the DRR in 70 liver samples. We found significant associations between DRR methylation and the expression of CYP3A5 and CYP3A7 but not CYP3A4, indicating differential CYP3A regulation by the DRR. Also, we observed a dynamic reduction in DRR DNA methylation during the differentiation of induced pluripotent stem cells to hepatocytes, which correlated with increased CYP3A expression. We then evaluated the relative contribution of genetic variants, TFs, and DRR DNA methylation on CYP3A expression in liver samples. Our results reinforce the DRR as a CYP3A regulator and suggest that DNA methylation may impact CYP3A-mediated drug metabolism.
CYP3A 是肝脏中重要的药物代谢酶。导致 CYP3A 表达/活性个体间差异很大的原因仍知之甚少。DNA 甲基化广泛调节基因表达,并且在胎儿 CYP3A7 向成人 CYP3A4 的发育转变中,CYP3A4 启动子上游的 CpG 甲基化与其表达相关。然而,由于非启动子 CYP3A 调节区域在很大程度上仍未被充分描述,因此 DNA 甲基化如何影响 CYP3A 表达仍有待充分探索。我们最近确定了一个控制 CYP3A4、CYP3A5 和 CYP3A7 表达的远端调节区 (DRR)。在这里,我们研究了 70 个肝组织样本中 DRR 内 16 个 CpG 位点的甲基化状态与 CYP3A 表达之间的关系。我们发现 DRR 甲基化与 CYP3A5 和 CYP3A7 的表达之间存在显著关联,但与 CYP3A4 的表达无关,这表明 DRR 对 CYP3A 的调节存在差异。此外,我们观察到在诱导多能干细胞向肝细胞分化过程中 DRR DNA 甲基化的动态减少,这与 CYP3A 表达的增加相关。然后,我们评估了遗传变异、TFs 和 DRR DNA 甲基化对肝组织样本中 CYP3A 表达的相对贡献。我们的结果强化了 DRR 作为 CYP3A 调节剂的作用,并表明 DNA 甲基化可能影响 CYP3A 介导的药物代谢。