α-TEA as a stimulator of tumor autophagy and enhancer of antigen cross-presentation

Autophagy. 2013 Mar;9(3):429-31. doi: 10.4161/auto.22969. Epub 2012 Dec 12.

Abstract

Stimulation of apoptosis has been reported as the primary mechanism of tumor cell death induced by alpha-tocopheryloxyacetic acid (α-TEA), an esterase-resistant, semi-synthetic derivative of vitamin E (R-R-R-α-tocopherol). New information now shows that α-TEA also triggers tumor cell autophagy and promotes antigen cross-presentation. Autophagosome-enriched fractions of α-TEA-treated tumor cells (α-TAGS) efficiently cross-primed antigen-specific CD8 (+) T cells and vaccination with dendritic cells (DC) pulsed with α-TAGS reduced lung metastases and increased survival of tumor-bearing mice. Taken together, these observations suggest that both autophagy and apoptosis signaling programs are activated in tumor cells by α-TEA treatment and may contribute to tumor cell death. We propose that autophagy-dependent enhancement of cross-presentation is a novel mechanism of α-TEA-mediated tumor immunity and that α-TEA can be exploited as an adjuvant to enhance the antitumor response.

Keywords: autophagy; cross-presentation; tumor immunity; vitamin E analog; α-TEA.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigen Presentation*
  • Apoptosis*
  • Autophagy / drug effects
  • Autophagy / physiology*
  • CD8-Positive T-Lymphocytes / cytology
  • Cell Line, Tumor
  • Cell Survival
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Mice
  • Microtubule-Associated Proteins / metabolism
  • Mitochondria / metabolism
  • Neoplasms / immunology
  • Neoplasms / pathology
  • Tocopherols / chemistry
  • Tocopherols / pharmacology*
  • Vitamin E / analogs & derivatives

Substances

  • Map1lc3b protein, mouse
  • Microtubule-Associated Proteins
  • Vitamin E
  • 2,5,7,8-tetramethyl-2R-(4R,8R,12-trimethyltridecyl)chroman-6-yloxy acetic acid
  • Tocopherols