EGFR inhibitors regulate Ca²⁺ concentration and apoptosis after PM_2.5 exposure based on a lung-mimic microfluidic...

Air pollution has side effects on human health. Epidemiology studies indicate a positive association between ambient fine particle (PM_2.5, or particles less than 2.5 μm in diameter) concentration and lung cancer. However, how fine particles affect lung cancer at the molecular level and related therapeutic methods to address these diseases are unclear. Here, the multi-omics analysis (DNA methylation and transcriptomic) was used to detect human bronchial epithelial cells (HBE), that were exposed to PM_2.5 using a quantified, small, portable, and organ-level air-liquid interface microfluidic system that mimics lung functions. The results indicate that 36,838 differentially methylated genes were detected. Of these 33,796 genes were hypomethylated (beta < 0), and 2862 genes were hypermethylated (beta > 0). RNA-Seq analysis demonstrated that 19,489 genes were upregulated (log₂FC > 0), and 16,659 were downregulated. Furthermore, the calcium and apoptosis pathways were activated according to multi-omics analysis. The change in EGFR gene expression after PM_2.5 exposure was the result of alterations of the cellular DNA methylome in the promoter. Inhibition or down-regulation of EGFR could result in the regulation of the downstream intracellular Ca²⁺ concentration and apoptosis via the EGFR/PLCγ and EGFR/STAT/Bcl-XL pathways after PM_2.5 exposure. EGFR inhibitors decrease the Ca²⁺ concentration of cells, thereby strengthening the effects of fine particles on apoptosis. In short, the Ca²⁺ concentration and the apoptosis of cells can be regulated via EGFR related pathway after PM_2.5 exposure. The EGFR may be a potentially promising therapeutic target for the treatment of air pollution-induced lung cancer through regulation of the intracellular Ca²⁺ concentration and apoptosis.