转录因子Sp1
发病机制
生物
转录因子
细胞生物学
炎症
计算生物学
基因
抄写(语言学)
生物信息学
发起人
癌症研究
基因表达
遗传学
免疫学
哲学
语言学
作者
Jie-Feng Jiang,Zheng‐Yang Zhou,Yizhang Liu,Li Wu,Binbin Nie,Liang Huang,Chi Zhang
标识
DOI:10.1007/s11033-022-07516-9
摘要
Specificity protein (Sp) is a famous family of transcription factors including Sp1, Sp2 and Sp3. Sp1 is the first one of Sp family proteins to be characterized and cloned in mammalian. It has been proposed that Sp1 acts as a modulator of the expression of target gene through interacting with a series of proteins, especially with transcriptional factors, and thereby contributes to the regulation of diverse biological processes. Notably, growing evidence indicates that Sp1 is involved in the main events in the development of atherosclerosis (AS), such as inflammation, lipid metabolism, plaque stability, vascular smooth muscle cells (VSMCs) proliferation and endothelial dysfunction. This review is designed to provide useful clues to further understanding roles of Sp1 in the pathogenesis of AS, and may be helpful for the design of novel efficacious therapeutics agents targeting Sp1.
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