PIKE-A Modulates Mitochondrial Metabolism through Increasing SDHA Expression Mediated by STAT3/FTO Axis

Int J Mol Sci. 2022 Sep 25;23(19):11304. doi: 10.3390/ijms231911304.

Abstract

Previous studies have shown that phosphoinositide 3-kinase enhancer-activating Akt (PIKE-A) is involved in the regulation of several biological processes in cancer. In our previous study, we demonstrated a crucial function of PIKE-A in cancer energy metabolism by regulating pentose phosphate pathway (PPP) flux. However, whether PIKE-A regulates energy metabolism through affecting mitochondrial changes are poorly understood. In the present study, we show that PIKE-A promotes mitochondrial membrane potential, leading to increasing proliferation of glioblastoma cell. Mechanistically, PIKE-A affects the expression of respiratory chain complex Ⅱ succinate dehydrogenase A (SDHA), mediated by regulating the axis of STAT3/FTO. Taken together, these results revealed that inhibition of PIKE-A reduced STAT3/FTO/SDHA expression, leading to the suppression of mitochondrial function. Thus, our findings suggest the PIKE-A/STAT3/FTO/SDHA axis as promising anti-cancer treatment targets.

Keywords: PIKE-A; SDHA; cell proliferation; glioblastoma; mitochondria.

MeSH terms

  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO / metabolism
  • Electron Transport Complex II / metabolism
  • Glioblastoma*
  • Humans
  • Mitochondria / metabolism
  • Phosphatidylinositol 3-Kinase / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt* / metabolism
  • STAT3 Transcription Factor / metabolism
  • Succinate Dehydrogenase / metabolism

Substances

  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Alpha-Ketoglutarate-Dependent Dioxygenase FTO
  • FTO protein, human
  • Electron Transport Complex II
  • SDHA protein, human
  • Succinate Dehydrogenase
  • Phosphatidylinositol 3-Kinase
  • Proto-Oncogene Proteins c-akt