Literature DB >> 22745370

The vitamin E analogue α-TEA stimulates tumor autophagy and enhances antigen cross-presentation.

Yuhuan Li1, Tobias Hahn, Kendra Garrison, Zhi-Hua Cui, Andrew Thorburn, Jacqueline Thorburn, Hong-Ming Hu, Emmanuel T Akporiaye.   

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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Year:  2012        PMID: 22745370      PMCID: PMC3576035          DOI: 10.1158/0008-5472.CAN-11-3103

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  49 in total

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Review 5.  Cross talk between apoptosis and autophagy by caspase-mediated cleavage of Beclin 1.

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Review 9.  Autophagy in blood cancers: biological role and therapeutic implications.

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Review 10.  Autophagy in cancer: moving from understanding mechanism to improving therapy responses in patients.

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