miR‐200b ameliorates myofibroblast transdifferentiation in precancerous oral submucous fibrosis through targeting <scp>ZEB</scp>2

Yi‐Wen LiaoCheng‐Chia YuPei‐Ling HsiehYu‐Chao Chang2026-01-272026-01-272018-06-1210.1111/jcmm.13690https://scholars.csmu.edu.tw/handle/123456789/3071AbstractOral submucous fibrosis (OSF) is a progressive scarring disease. MicroRNA‐200b (miR‐200b) has been reported as a tumour suppressor, but its role in the precancerous OSF remains unknown. In this study, we investigated the impact of miR‐200b on myofibroblastic differentiation activity. Arecoline is a major areca nut alkaloid and has been employed to induce the elevated myofibroblast activity in human buccal mucosal fibroblasts (BMFs). Treatment of arecoline in BMFs dose‐dependently reduced gene expression of miR‐200b, which corresponded with the decreased expression of miR‐200b in fBMFs. The arecoline‐induced myofibroblast activities were abolished by overexpression of miR‐200b in BMFs, and the same results were observed in fBMFs. In addition, α‐SMA was inhibited by an increase in miR‐200b. We further demonstrated that miR‐200b‐mediated decrease in ZEB2 led to down‐regulation of α‐SMA, vimentin. Loss of miR‐200b resulted in enhanced collagen contraction and migration capabilities, and knockdown of ZEB2 reversed these phenomena. Lastly, we showed the expression of miR‐200b was significantly less and ZEB2 was markedly higher in OSF tissues. These results suggested that down‐regulation of miR‐200b may contribute to the pathogenesis of areca quid‐associated OSF through the regulation of ZEB2 and myofibroblast hallmarks.[SDGs]SDG3miR‐200b ameliorates myofibroblast transdifferentiation in precancerous oral submucous fibrosis through targeting <scp>ZEB</scp>2journal-article