西斯特
肌成纤维细胞
下调和上调
癌症研究
基因沉默
纤维化
长非编码RNA
生物
口腔粘膜下纤维性变
细胞生物学
化学
病理
医学
遗传学
X-失活
基因
X染色体
作者
Chuan‐Hang Yu,Pei‐Ling Hsieh,Shih-Chi Chao,Szu-Han Chen,Yi‐Wen Liao,Cheng‐Chia Yu
标识
DOI:10.1016/j.ijbiomac.2023.123400
摘要
Long non-coding RNA XIST promotes the development of various types of head and neck cancers, but its role in the progression of precancerous oral submucous fibrosis (OSF) has not been determined yet. As such, we aimed to examine whether XIST implicates in the regulation of myofibroblast activation. Our results showed that the expression of XIST was upregulated in OSF tissues and fibrotic buccal mucosal fibroblasts (fBMFs), and the silencing of XIST downregulated several myofibroblasts features. We demonstrated that elevation of let-7i after inhibition of XIST may lead to reduced myofibroblast activation. On the contrary, overexpression of high mobility group AT-Hook 1 (HMGA1) following the suppression of let-7i may result in enhanced myofibroblast activities. Moreover, we showed that the suppressive effect of silencing of XIST on myofibroblasts hallmarks was reversed by let-7i inhibition or HMGA1 overexpression, suggesting the pro-fibrotic property of XIST was mediated by downregulation of let-7i and upregulation of HMGA1. These findings revealed that myofibroblast activation of fBMFs may attribute to the alteration of the XIST/let-7i/HMGA1 axis. Therapeutic approaches to target this axis may serve as a promising direction to ameliorate the malignant progression of OSF.
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