Disco interacting protein 2 homolog A (DIP2A): A key component in the regulation of brain disorders.

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. • DIP2A plays multiple functions in neurological disorders. • DIP2A regulates various biological processes including oxidative stress, and apoptosis. • The role of DIP2A in brain disorders is understudied and more studies are required for more understanding. • Controlling DIP2A could help design effective diagnostic and therapeutic approaches for brain disorders. [ABSTRACT FROM AUTHOR]