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Nuclear FAK controls chemokine transcription, Tregs, and evasion of anti-tumor immunity.

Cell | 2015

Focal adhesion kinase (FAK) promotes anti-tumor immune evasion. Specifically, the kinase activity of nuclear-targeted FAK in squamous cell carcinoma (SCC) cells drives exhaustion of CD8(+) T cells and recruitment of regulatory T cells (Tregs) in the tumor microenvironment by regulating chemokine/cytokine and ligand-receptor networks, including via transcription of Ccl5, which is crucial. These changes inhibit antigen-primed cytotoxic CD8(+) T cell activity, permitting growth of FAK-expressing tumors. Mechanistically, nuclear FAK is associated with chromatin and exists in complex with transcription factors and their upstream regulators that control Ccl5 expression. Furthermore, FAK's immuno-modulatory nuclear activities may be specific to cancerous squamous epithelial cells, as normal keratinocytes do not have nuclear FAK. Finally, we show that a small-molecule FAK kinase inhibitor, VS-4718, which is currently in clinical development, also drives depletion of Tregs and promotes a CD8(+) T cell-mediated anti-tumor response. Therefore, FAK inhibitors may trigger immune-mediated tumor regression, providing previously unrecognized therapeutic opportunities.

Pubmed ID: 26406376 RIS Download

Research resources used in this publication

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Associated grants

  • Agency: Wellcome Trust, United Kingdom
    Id: 095831
  • Agency: Medical Research Council, United Kingdom
    Id: G0900992
  • Agency: Medical Research Council, United Kingdom
    Id: G1100084
  • Agency: Cancer Research UK, United Kingdom
    Id: C157/A15703

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