Cyclophilin A as a downstream effector of PI3K/Akt signalling pathway in multiple myeloma cells

Cell Biochem Funct. 2015 Dec;33(8):566-74. doi: 10.1002/cbf.3156.

Abstract

Cyclophilin A (Cyp A), a member of the peptidyl-prolyl isomerase (PPI) family, may function as a molecular signalling switch. Comparative proteomic studies have identified Cyp A as a potential downstream target of protein kinase B (Akt). This study confirmed that Cyp A is a downstream effector of the phosphatidylinositide 3-kinase (PI3K)/Akt signalling pathway. Cyp A was highly phosphorylated in response to interleukin-6 treatment, which was consistent with the accumulation of phosphorylated Akt, suggesting that Cyp A is a phosphorylation target of Akt and downstream effector of the PI3K/Akt pathway. Cyclosporine A (CsA), a PPI inhibitor, inhibited the growth of multiple myeloma (MM) U266 cells. Moreover, CsA treatment inhibited the activation of the signal transducer and activator of transcription 3 (STAT3) in MM U266 cells. Several Cyp A mutants were generated. Mutants with mutated AKT phosphorylation sites increased the G1 phase arrest in MM U266 cells. The other mutants that mimicked the phosphorylated state of Cyp A decreased the percentage of G1 phase. These results demonstrated that the states of phosphorylation of Cyp A by Akt can influence the progress of the cell cycle in MM U266 cells and that this effect is probably mediated through the Janus-activated kinase 2/STAT3 signalling pathway.

Keywords: AKT; JAK2; STAT3; cyclophilin A; interleukin-6; multiple myeloma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cyclophilin A / chemistry
  • Cyclophilin A / genetics
  • Cyclophilin A / metabolism*
  • Cyclosporine / pharmacology
  • DNA Mutational Analysis
  • Humans
  • Hydroxybenzoates / pharmacology
  • Molecular Sequence Data
  • Multiple Myeloma / metabolism*
  • Multiple Myeloma / pathology
  • Mutant Proteins / chemistry
  • Mutant Proteins / metabolism
  • Nitrofurans / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / metabolism*
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction* / drug effects

Substances

  • Hydroxybenzoates
  • Mutant Proteins
  • Nitrofurans
  • STAT3 Transcription Factor
  • Cyclosporine
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • Cyclophilin A
  • nifuroxazide