MedicineMolecular BiologyOncologyApoptosisCarcinogenesisMolecular OncologyCancer Cell SignalingCell Cycle SignalingCell-cycle CheckpointsCell-cycle DysregulationNoncoding Rna In CancerOncogenic Signaling PathwaysCell Proliferation IndicesMicrorna Function In CancerMicrorna-mediated OncogenesisMicrorna-mediated Pathway RegulationNon-small Cell Lung Cancer TherapyWee1 InhibitionWee1 Kinase RegulationWee1 Kinase Signaling
Circular RNA-synaptosome associated protein 47 (circ-SNAP47; Hsa_circ_0016760) is oncogenic in non-small-cell lung cancer (NSCLC); however, its role is undescribed in cis-diamminedichloroplatinum II (DDP) resistance. We attempted to investigate its expression, role and mechanism in DDP-tolerant NSCLC. As a result, circ-SNAP47 expression was upregulated in human DDP-tolerant NSCLC tissues and cells, accompanied with WEE1 G2 checkpoint kinase (WEE1) upregulation and microRNA (miR)-625-5p downregulation. Functionally, interfering circ-SNAP47 and/or restoring miR-625-5p curbed the 50% inhibitory concentration of DDP, colony formation, cell proliferation and invasion, accompanied with apoptotic rate promotion and depressions of multidrug resistance (MDR) markers MDR1 and MRP1, anti-apoptosis protein Bcl-2, and pro-invasion protein MMP9. Notably, circ-SNAP47 interference suppressed xenograft tumor growth of DDP-tolerant NSCLC cells by elevating miR-625-5p and descending WEE1. Mechanistically, circ-SNAP47 directly targeted miR-625-5p, and miR-625-5p further targeted WEE1. Therefore, circ-SNAP47-miR-625-5p-WEE1 axis might participate in chemoresistance and progression of DDP-tolerant NSCLC.
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Yongsheng Li, Jiahang Hu, Lijuan Li et al. · Biochemical and Biophysical Research Communications · 2018 · 131 citations
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Medicine, Oncology, Pharmacology +15