Convallatoxin, a dual inducer of autophagy and apoptosis, inhibits angiogenesis in vitro and in vivo

PLoS One. 2014 Mar 24;9(3):e91094. doi: 10.1371/journal.pone.0091094. eCollection 2014.

Abstract

Autophagy and apoptosis are important processes that control cellular homeostasis and have been highlighted as promising targets for novel cancer therapies. Here, we identified convallatoxin (CNT), isolated from Antiaris toxicaria, as a dual inducer of autophagy and apoptosis. CNT exerts cytotoxic effects on a number of cancer and normal cell lines and induces apoptosis by increasing caspase-3 and poly ADP ribose polymerase (PARP) cleavage. Moreover, dose- and time-dependent autophagic activity was detected in CNT-treated cells, and mammalian target of rapamycin (mTOR)/p70S6K signal pathway inhibition was observed. Notably, CNT inhibits human umbilical vein endothelial cell (HUVEC) growth and exerts anti-angiogenic activity in vitro and in vivo. Collectively, these results demonstrate that the naturally occurring compound, CNT, is a novel anti-angiogenic compound via dual inducing of autophagy and apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / pharmacology*
  • Angiogenesis Inhibitors / therapeutic use
  • Antiaris / chemistry
  • Apoptosis / drug effects*
  • Autophagy / drug effects*
  • Cell Line
  • Human Umbilical Vein Endothelial Cells / cytology
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Humans
  • Neovascularization, Pathologic / drug therapy*
  • Signal Transduction / drug effects
  • Strophanthins / pharmacology*
  • Strophanthins / therapeutic use
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Angiogenesis Inhibitors
  • Strophanthins
  • TOR Serine-Threonine Kinases
  • convallatoxin

Grants and funding

This study was partly supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIP; 2009-0092964, 2009-0083522, 2011-0006165, 2012M3A9D1054520), the Center for Food and Drug Materials of Agriculture Science & Technology Development (PJ0079772012), the Rural Development Administration, the National R&D Program, the Ministry of Health & Welfare (0620360-1), and the Brain Korea 21 Plus Project. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.