Abstract
Immunotherapeutic interventions are showing effectiveness across a wide range of cancer types, but only a subset of patients shows clinical response to therapy. Responsiveness to checkpoint blockade immunotherapy is favoured by the presence of a local, CD8+ T cell-based immune response within the tumour microenvironment. As molecular analyses of tumours containing or lacking a productive CD8+ T cell infiltrate are being pursued, increasing evidence is indicating that activation of oncogenic pathways in tumour cells can impair induction or execution of a local antitumour immune response. This Review summarizes our current knowledge of the influence of oncogenic effects on evasion of antitumour immunity.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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AMP-Activated Protein Kinase Kinases
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CD8-Positive T-Lymphocytes / drug effects
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Genes, myc / immunology
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Humans
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Immunotherapy / methods
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Lymphocyte Activation
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Lymphocytes, Tumor-Infiltrating / immunology
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Lymphocytes, Tumor-Infiltrating / pathology
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Neoplasms / immunology*
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Neoplasms / therapy*
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Oncogenes / immunology*
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Oncogenes / physiology
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PTEN Phosphohydrolase / genetics
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PTEN Phosphohydrolase / immunology
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PTEN Phosphohydrolase / metabolism
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Protein Serine-Threonine Kinases / genetics
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Protein Serine-Threonine Kinases / immunology
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Protein Serine-Threonine Kinases / metabolism
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Tumor Escape*
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Wnt Signaling Pathway
Substances
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Protein Serine-Threonine Kinases
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STK11 protein, human
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AMP-Activated Protein Kinase Kinases
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PTEN Phosphohydrolase
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PTEN protein, human