MTCH2 in Metabolic Diseases, Neurodegenerative Diseases, Cancers, Embryonic Development and Reproduction

Drug Des Devel Ther. 2024 Jun 12:18:2203-2213. doi: 10.2147/DDDT.S460448. eCollection 2024.

Abstract

Mitochondrial carrier homolog 2 (MTCH2) is a member of the solute carrier 25 family, located on the outer mitochondrial membrane. MTCH2 was first identified in 2000. The development in MTCH2 research is rapidly increasing. The most well-known role of MTCH2 is linking to the pro-apoptosis BID to facilitate mitochondrial apoptosis. Genetic variants in MTCH2 have been investigated for their association with metabolic and neurodegenerative diseases, however, no intervention or therapeutic suggestions were provided. Recent studies revealed the physiological and pathological function of MTCH2 in metabolic diseases, neurodegenerative diseases, cancers, embryonic development and reproduction via regulating mitochondrial apoptosis, metabolic shift between glycolysis and oxidative phosphorylation, mitochondrial fusion/fission, epithelial-mesenchymal transition, etc. This review endeavors to assess a total of 131 published articles to summarise the structure and physiological/pathological role of MTCH2, which has not previously been conducted. This review concludes that MTCH2 plays a crucial role in metabolic diseases, neurodegenerative diseases, cancers, embryonic development and reproduction, and the predominant molecular mechanism is regulation of mitochondrial function. This review gives a comprehensive state of current knowledgement on MTCH2, which will promote the therapeutic research of MTCH2.

Keywords: BID; MTCH2; Mimp; apoptosis; mitochondrial carrier homolog 2.

Publication types

  • Review

MeSH terms

  • Animals
  • Embryonic Development*
  • Humans
  • Metabolic Diseases* / metabolism
  • Mitochondria / metabolism
  • Mitochondrial Membrane Transport Proteins / metabolism
  • Neoplasms* / metabolism
  • Neoplasms* / pathology
  • Neurodegenerative Diseases* / metabolism
  • Reproduction*

Substances

  • Mitochondrial Membrane Transport Proteins

Grants and funding

XP received a National Natural Science Foundation of China (NSFC-82000399) and YC received a research grant from the National Key Research and Development Program of China (2022YFC2703000).