The Vitamin E Analogue α-TEA Stimulates Tumor Autophagy and Enhances Antigen Cross-Presentation

Yuhuan Li(Providence Portland Medical Center), Tobias Hahn(Providence Portland Medical Center), Kendra Garrison(Providence Portland Medical Center), Zhi-Hua Cui(Providence Portland Medical Center), Andrew Thorburn(Providence Portland Medical Center), Jacqueline Thorburn(Providence Portland Medical Center), Hong‐Ming Hu(Providence Portland Medical Center), Emmanuel T. Akporiaye(Providence Portland Medical Center)
Cancer Research
June 29, 2012
Cited by 84Open Access
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Abstract

The semisynthetic vitamin E derivative alpha-tocopheryloxyacetic acid (α-TEA) induces tumor cell apoptosis and may offer a simple adjuvant supplement for cancer therapy if its mechanisms can be better understood. Here we report that α-TEA also triggers tumor cell autophagy and that it improves cross-presentation of tumor antigens to the immune system. α-TEA stimulated both apoptosis and autophagy in murine mammary and lung cancer cells and inhibition of caspase-dependent apoptosis enhanced α-TEA-induced autophagy. Cell exposure to α-TEA generated double-membrane-bound vesicles indicative of autophagosomes, which efficiently cross-primed antigen-specific CD8(+) T cells. Notably, vaccination with dendritic cells pulsed with α-TEA-generated autophagosomes reduced lung metastases and increased the survival of tumor-bearing mice. Taken together, our findings suggest that both autophagy and apoptosis signaling programs are activated during α-TEA-induced tumor cell killing. We suggest that the ability of α-TEA to stimulate autophagy and enhance cross-priming of CD8(+) T cells might be exploited as an adjuvant strategy to improve stimulation of antitumor immune responses.


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