安普克
PI3K/AKT/mTOR通路
神经科学
蛋白激酶B
生物
信号转导
上游和下游(DNA)
神经退行性变
疾病
医学
细胞生物学
蛋白激酶A
激酶
上游(联网)
病理
计算机网络
计算机科学
作者
Baoyuan Zhang,Xuesong Zhang,Moussa Omorou,Kai Zhao,Yang Ruan,Hemi Luan
标识
DOI:10.1016/j.biopha.2023.115771
摘要
Disco Interacting Protein 2 Homolog A (DIP2A) is expressed throughout the body and abundantly expressed in the brain tissue. It is activated by Follistatin-like 1 (FSTL1). Activated DIP2A interacts with several pathways, such as AMPK/mTOR and AKT pathways, to contribute to many biological processes, such as oxidative stress, transcriptional regulation, and apoptosis. Dysregulated DIP2A activation has been implicated in numerous processes in the brain. If the upstream pathways of DIP2A remain globally unexplored, many proteins, including cortactin, AMPK, and AKT, have been identified as its downstream targets in the literature. Recent studies have linked DIP2A to a variety of mechanisms in many types of brain disorders, suggesting that regulation of DIP2A could provide novel diagnostic and therapeutic approaches for brain disorders. In this review, we comprehensively summarized and discussed the current research on DIP2A in various brain disorders, such as stroke, autism spectrum disorders (ASD), Alzheimer's disease (AD), dyslexia, and glioma.
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