Profilin upregulation induces autophagy through stabilization of AMP-activated protein kinase

FEBS Lett. 2022 Jul;596(14):1765-1777. doi: 10.1002/1873-3468.14372. Epub 2022 May 25.

Abstract

Profilin regulates actin polymerization, and its balanced expression is required for cellular growth and development. Most tumours have compromised profilin expression, and its overexpression in MDA MB-231 breast cancer cells has been reported to activate AMP-activated protein kinase α (AMPKα), an energy-sensing molecule that affects various cellular processes including autophagy. This study aims to explore the role of profilin in autophagy induction. We employed all-trans retinoic acid (ATRA) as an inducer of profilin expression and showed that profilin induces autophagy through mTOR inhibition, autophagy-activating kinase ULK1 upregulation, and AMPK stabilization as well as its activation. Furthermore, evidence from our study indicates physical interaction between profilin and AMPK, which results in AMPK stabilization and induction of prolonged autophagy, thereby leading to apoptosis. This study uncovers a novel mechanism that induces autophagy in triple-negative breast cancer cells.

Keywords: AMP-activated protein kinase; LAMP 2; LC3; autophagy; profilin; retinoic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases* / genetics
  • AMP-Activated Protein Kinases* / metabolism
  • Autophagy
  • Autophagy-Related Protein-1 Homolog / metabolism
  • Profilins* / genetics
  • Up-Regulation

Substances

  • Profilins
  • Autophagy-Related Protein-1 Homolog
  • AMP-Activated Protein Kinases