Oral submucous fibrosis: pathogenesis and therapeutic approaches

被引:0
|
作者
Tang, Jianfei [1 ,2 ,3 ,4 ,5 ]
Liu, Junjie [1 ,2 ,3 ,4 ,5 ]
Zhou, Zekun [1 ,2 ,3 ,4 ,5 ]
Cui, Xinyan [1 ,2 ,3 ,4 ,5 ]
Tu, Hua [1 ,2 ,3 ,4 ,5 ]
Jia, Jia [1 ,2 ,3 ,4 ,5 ]
Chen, Baike [1 ,2 ,3 ,4 ,5 ]
Dai, Xiaohan [1 ,2 ,3 ,4 ,5 ]
Liu, Ousheng [1 ,2 ,3 ,4 ,5 ]
机构
[1] Cent South Univ, Hunan Key Lab Oral Hlth Res, Changsha, Peoples R China
[2] Cent South Univ, Hunan 3D Printing Engn Res Ctr Oral Care, Changsha, Peoples R China
[3] Cent South Univ, Hunan Clin Res Ctr Oral Major Dis & Oral Hlth & Ac, Changsha, Peoples R China
[4] Cent South Univ, Xiangya Stomatol Hosp, Changsha, Peoples R China
[5] Cent South Univ, Xiangya Sch Stomatol, Changsha, Peoples R China
基金
中国国家自然科学基金;
关键词
BUCCAL MUCOSAL FIBROBLASTS; POTENTIALLY MALIGNANT DISORDERS; IRREPARABLE DNA-DAMAGE; SUB-MUCOUS FIBROSIS; ARECA NUT; BETEL-QUID; GROWTH-FACTOR; IN-VITRO; MYOFIBROBLAST ACTIVITIES; MESENCHYMAL TRANSITION;
D O I
10.1038/s41368-024-00344-6
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Oral submucous fibrosis (OSF), characterized by excessive deposition of extracellular matrix (ECM) that causes oral mucosal tissue sclerosis, and even cancer transformation, is a chronic, progressive fibrosis disease. However, despite some advancements in recent years, no targeted antifibrotic strategies for OSF have been approved; likely because the complicated mechanisms that initiate and drive fibrosis remain to be determined. In this review, we briefly introduce the epidemiology and etiology of OSF. Then, we highlight how cell-intrinsic changes in significant structural cells can drive fibrotic response by regulating biological behaviors, secretion function, and activation of ECM-producing myofibroblasts. In addition, we also discuss the role of innate and adaptive immune cells and how they contribute to the pathogenesis of OSF. Finally, we summarize strategies to interrupt key mechanisms that cause OSF, including modulation of the ECM, inhibition of inflammation, improvement of vascular disturbance. This review will provide potential routes for developing novel anti-OSF therapeutics.
引用
收藏
页数:15
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