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The dual role of IRF8 in cancer immunosurveillance

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Article: e25476 | Received 19 Jun 2013, Accepted 19 Jun 2013, Published online: 01 Jul 2013

Figures & data

Figure 1. Dual role of IRF8 in cancer immunosurveillance. In comparison to immunocompetent (wild-type) hosts, interferon-regulatory factor 8 (IRF8)-deficient mice receiving B16.F10 melanoma cells exhibit accelerated tumor growth and an increased propensity to form lung metastasis. For the most part, this reflects the establishment of a highly immunosuppressive tumor microenvironment characterized by the expression of cytokines, chemokines, and pro-angiogenic factors that support tumor growth and metastasis. All these events are closely correlated with the epigenetic silencing of Irf8 in melanoma cells.

Figure 1. Dual role of IRF8 in cancer immunosurveillance. In comparison to immunocompetent (wild-type) hosts, interferon-regulatory factor 8 (IRF8)-deficient mice receiving B16.F10 melanoma cells exhibit accelerated tumor growth and an increased propensity to form lung metastasis. For the most part, this reflects the establishment of a highly immunosuppressive tumor microenvironment characterized by the expression of cytokines, chemokines, and pro-angiogenic factors that support tumor growth and metastasis. All these events are closely correlated with the epigenetic silencing of Irf8 in melanoma cells.