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

Biomed Pharmacother. 2023 Dec:168:115771. doi: 10.1016/j.biopha.2023.115771. Epub 2023 Oct 26.

Abstract

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.

Keywords: Brain; Brain disorders; DIP2A; Mitochondria; Oxidative stress.

Publication types

  • Review

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Brain Diseases*
  • Follistatin-Related Proteins* / metabolism
  • Gene Expression Regulation
  • Humans
  • Nuclear Proteins / genetics
  • Proto-Oncogene Proteins c-akt / metabolism

Substances

  • Proto-Oncogene Proteins c-akt
  • AMP-Activated Protein Kinases
  • Nuclear Proteins
  • FSTL1 protein, human
  • Follistatin-Related Proteins
  • DIP2A protein, human