α-Tocopheryl succinate stabilizes the structure of tumor vessels by inhibiting angiopoietin-2 expression

Biochem Biophys Res Commun. 2020 Jan 22;521(4):947-951. doi: 10.1016/j.bbrc.2019.11.017. Epub 2019 Nov 11.

Abstract

α-Tocopheryl succinate (TS) is a tocopherol derivative and has multifaceted anti-cancer effects; TS not only causes cancer cell-specific apoptosis but also inhibits tumor angiogenesis. Although TS has the potential to be used as a well-tolerated anti-angiogenic drug, it is still unclear which step of the angiogenic process is inhibited by TS. Here, we show that TS inhibits the expression of angiopoietin (Ang)-2, which induces destabilization of vascular structure in the initial steps of the angiogenic process. In mouse melanoma cells, TS treatment decreased mRNA and extracellular protein levels of Ang-2; however, the mRNA level of Ang-1, which stabilizes the vascular structure, remained unchanged. Furthermore, aorta ring and Matrigel plug angiogenesis assays indicated that the conditioned medium from TS-treated cells (CM-TS) inhibited neovascularization and blood leakage from the existing blood vessels, respectively. Following immunohistochemical staining of the vessels treated with CM-TS, imaging studies showed that the vascular endothelial cells were highly packed with pericytes. In conclusion, we found that TS inhibits Ang-2 expression and, consequently, stabilizes the vascular structure during the initial step of tumor angiogenesis.

Keywords: Angiogenesis; Angiopoietin; Tocopheryl succinate; Vascular stabilization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / chemistry
  • Angiogenesis Inhibitors / pharmacology*
  • Angiopoietin-1 / metabolism
  • Angiopoietin-2 / antagonists & inhibitors*
  • Angiopoietin-2 / metabolism
  • Animals
  • Aorta / drug effects
  • Cell Line, Tumor
  • Culture Media, Conditioned / pharmacology
  • Humans
  • Male
  • Melanoma / blood supply
  • Melanoma / drug therapy
  • Melanoma / pathology
  • Mice
  • Mice, Inbred BALB C
  • Neovascularization, Pathologic / drug therapy*
  • Neovascularization, Pathologic / pathology
  • Structure-Activity Relationship
  • alpha-Tocopherol / chemistry
  • alpha-Tocopherol / pharmacology*

Substances

  • Angiogenesis Inhibitors
  • Angiopoietin-1
  • Angiopoietin-2
  • Angpt1 protein, mouse
  • Angpt2 protein, mouse
  • Culture Media, Conditioned
  • alpha-Tocopherol