The effect of indatraline on angiogenesis suppression through HIF-1α-mediated VEGF inhibition

Biochem Biophys Res Commun. 2017 Apr 1;485(2):349-354. doi: 10.1016/j.bbrc.2017.02.077. Epub 2017 Feb 17.

Abstract

The present research reports a novel biological activity of indatraline, a compound clinically used as an antidepressant. We previously identified indatraline as an autophagy inducer. Autophagy is an intracellular catabolic pathway for degrading or recycling unnecessary organelles in response to cellular stress. Indatraline-mediated autophagy induction results from mTOR inhibition. The mTOR is a negative regulator of autophagy as well as a master regulator of angiogenesis. Angiogenesis defines the process by which new vessels are formed from pre-existing vascular tissues, providing nutrients to cancer cells, allowing rapid tumor progression. Accordingly, targeting angiogenesis to prevent cancer is an attractive therapeutic strategy. Here, we demonstrate that indatraline possibly acts to suppress tumor-mediated angiogenesis via downregulation of HIF-1α-mediated VEGF expression. The effects of indatraline on autophagy and angiogenesis could make it a potential drug candidate toward cancer treatment.

Keywords: Angiogenesis; Anticancer; Autophagy; HIF-1α; mTOR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / chemistry
  • Angiogenesis Inhibitors / pharmacology
  • Animals
  • Autophagy / drug effects
  • Cell Hypoxia
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Chick Embryo
  • Chorioallantoic Membrane / blood supply
  • Chorioallantoic Membrane / drug effects
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • HeLa Cells
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / physiology
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Immunoblotting
  • Indans / chemistry
  • Indans / pharmacology*
  • Methylamines / chemistry
  • Methylamines / pharmacology*
  • Molecular Structure
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / prevention & control*
  • Neovascularization, Physiologic / drug effects
  • Vascular Endothelial Growth Factor A / metabolism*

Substances

  • Angiogenesis Inhibitors
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Indans
  • Methylamines
  • Vascular Endothelial Growth Factor A
  • indatraline