Nalini Devi VerusingamYi-Chen ChenHeng-Fu LinChao-Yu LiuMing-Cheng LeeKai-Hsi LuCheong Soon KengAlan Ong Han KiatShih-Hwa ChiouMong-Lien Wang2024-11-062024-11-062020-10-01https://doi:10.1097/JCMA.0000000000000438https://dspace-cris.utar.edu.my/handle/123456789/6384<jats:sec> <jats:title>Background:</jats:title> <jats:p>Lung cancer contributes to high cancer mortality worldwide with 80% of total cases diagnosed as non-small cell lung cancer (NSCLC). Epidermal growth factor receptor (EGFR) tyrosine kinase (TK) domain serves as a druggable target in NSCLC patients with exon 19 deletion and L858R mutation. However, patients eventually succumbed to resistance to first- and second-generation EGFR-TK inhibitors through activation of T790M mutation. Third-generation EGFR-TKI, Osimertinib exhibits high efficacy in patients with exon 19 deletion/L858R/T790M mutation but they experienced acquired resistance thereafter. Available treatment options in NSCLC patients remains a challenge due to unknown molecular heterogeneity responsible for acquired resistance to EGFR-TKI. In this study, we aim to generate Osimertinib-resistant (OR) cells from H1975 carrying L858R/T790M double mutation which can be used as a model to elucidate mechanism of resistance.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods:</jats:title> <jats:p>OR cells were established via stepwise-dose escalation and limiting single-cell dilution method. We then evaluated Osimertinib resistance potential via cell viability assay. Proteins expression related to EGFR-signalling, epithelial to mesenchymal transition (EMT), and autophagy were analyzed via western blot.</jats:p> </jats:sec> <jats:sec> <jats:title>Results:</jats:title> <jats:p>OR cell lines exhibited increased drug resistance potential compared to H1975. Distinguishable mesenchymal-like features were observed in OR cells. Protein expression analysis revealed EGFR-independent signaling involved in the derived OR cells as well as EMT and autophagy activity.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusion:</jats:title> <jats:p>We generated OR cell lines <jats:italic toggle="yes">in-vitro</jats:italic> as evidenced by increased drug resistance potential, increased mesenchymal features, and enhanced autophagy activity. Development of Osimertinib resistance cells may serve as <jats:italic toggle="yes">in-vitro</jats:italic> model facilitating discovery of molecular aberration present during acquired mechanism of resistance.</jats:p> </jats:sec>journal-article