PM2.5 promotes non-small cell lung cancer tumorigenesis by miR-21-5p targeting PDE4DIP accumulated.

Background: Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related mortality worldwide. Fine particulate matter (PM2.5) is associated with increased risk of lung cancer. microRNAs (miRNAs) play an important role in a variety of cancers, including NSCLC. In NSCLC, existing literature has revealed upregulation of miR-21-5p. Nonetheless, the molecular mechanism of miR-21-5p in NSCLC development after PM2.5 exposure is not clear. This study aimed to investigate the role of miR-21-5p in NSCLC development after PM2.5 exposure and to elucidate the underlying molecular mechanisms. Methods: Expression of miR-21-5p, PDE4DIP, and SORBS2 was determined in NSCLC cell lines and tumor tissues. To measure proliferation, migration/invasion of NSCLC cells, 3-(4, 5-dimethyl-thiazolyl-2)-2, 5-diphenyl-tetrazolium bromide (MTT), colony formation, transwell and wound healing assays were accordingly performed. A tumor xenograft model was established to evaluate the effects of miR-21-5p, PDE4DIP, and SORBS2 modification on tumor growth in vivo. Results: miR-21-5p was up-regulated in NSCLC tumor tissues and cell lines. Also, PM2.5 exposure led to a higher level of miR-21-5p. The miR-21-5p mimic and inhibitor respectively promoted and decreased proliferation and migration/invasion of NSCLC cells. Tumor growth was reduced in miR-21-5p KO mice in vivo. Luciferase reporter assay indicated that PDE4DIP was a target of miR-21-5p. Moreover, miR-21-5p regulated cell proliferation and migration/invasion by inhibiting PDE4DIP expression after PM2.5 exposure. PDE4DIP knockdown promoted tumor growth in vivo. PDE4DIP and SORBS2 were down-regulated in NSCLC tumor tissues and cell lines. SORBS2 inhibited NSCLC cell proliferation and invasion/migration and tumor growth after PM2.5 exposure by regulating miR-21-5p/PDE4DIP signaling pathway. Conclusions: miR-21-5p could target PDE4DIP and promote tumor growth of NSCLC. SORBS2 suppressed NSCLC tumorigenesis by regulating miR-21-5p/PDE4DIP signaling pathway.