The molecular genetics of anterior segment dysgenesis

被引:7
|
作者
Kuang, Longhao [1 ,4 ]
Zhang, Min [2 ]
Wang, Ting [1 ,5 ]
Huang, Tao [1 ]
Li, Jin [1 ]
Gan, Run [1 ]
Yu, Mingyu [3 ]
Cao, Wenchao [3 ]
Yan, Xiaohe [1 ]
机构
[1] Jinan Univ, Shenzhen Eye Hosp, Shenzhen Eye Inst, Shenzhen 518040, Peoples R China
[2] Anhui Univ Sci & Technol, Sch Med, Huainan 232000, Peoples R China
[3] Jinan Univ, Shenzhen Eye Hosp, Dept Clin Med Coll 2, Shenzhen 518020, Peoples R China
[4] Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, State Key Lab Ophthalmol, Guangzhou, Peoples R China
[5] Songgang Peoples Hosp, Dept Ophthalmol, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
Anterior segment dysgenesis; Genetics; Molecular mechanism; AXENFELD-RIEGER-SYNDROME; TRANSCRIPTION FACTORS; COL4A1; MUTATION; EYE DEVELOPMENT; CYP1B1; ANIRIDIA; FOXC1; PEROXIDASIN; GLAUCOMA; PROTEIN;
D O I
10.1016/j.exer.2023.109603
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Anterior segment dysgenesis is a severe developmental eye disorder that leads to blindness in children. The exact mechanisms underlying this condition remain elusive. Recently, an increasing amount of studies have focused on genes and signal transduction pathways that affect anterior segment dysgenesis;these factors include transcription factors, developmental regulators, extracellular matrix genes, membrane-related proteins, cytoskeleton proteins and other associated genes. To date, dozens of gene variants have been found to cause anterior segment dysgenesis. However, there is still a lack of effective treatments. With a broader and deeper understanding of the molecular mechanisms underlying anterior segment development in the future, gene editing technology and stem cell technology may be new treatments for anterior segment dysgenesis. Further studies on the mechanisms of how different genes influence the onset and progression of anterior segment dysgenesis are still needed.
引用
收藏
页数:9
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