Nature Communications · 2017 · 62 citations · 54 references
MedicineImmunologyOncologyCancer ImmunologyImmunotherapyInflammationCancer Cell SignalingCancer ImmunotherapyImmune Cell SignalingInflammation-associated CarcinogenesisInflammatory SignalingTumor ImmunopathologyHepatocellular Carcinoma PathogenesisHepatocyte ProliferationInflammation-driven ProgressionInflammation-driven Tumor ProgressionInflammation-mediated CarcinogenesisNkg2 Receptor SignalingPro-tumorigenic SignalingTumor-associated Inflammation
Abstract Inflammation is recognized as one of the drivers of cancer. Yet, the individual immune components that possess pro- and anti-tumorigenic functions in individual cancers remain largely unknown. NKG2D is a potent activating immunoreceptor that has emerged as an important player in inflammatory disorders besides its well-established function as tumour suppressor. Here, we provide genetic evidence of an unexpected tumour-promoting effect of NKG2D in a model of inflammation-driven liver cancer. Compared to NKG2D-deficient mice, NKG2D-sufficient mice display accelerated tumour growth associated with, an increased recruitment of memory CD8 + T cells to the liver and exacerbated pro-inflammatory milieu. In addition, we show that NKG2D contributes to liver damage and consequent hepatocyte proliferation known to favour tumorigenesis. Thus, the NKG2D/NKG2D-ligand pathway provides an additional mechanism linking chronic inflammation to tumour development in hepatocellular carcinoma. Our findings expose the need to selectively target the types of cancer that could benefit from NKG2D-based immunotherapy.
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Jennifer Couzin-Frankel · Science · 2013 · 2K citations
Medicine, Immunology, Oncology +13
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Tumour-derived soluble MIC ligands impair expression of NKG2D and T-cell activation
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Rae1 and H60 ligands of the NKG2D receptor stimulate tumour immunity
Andreas Diefenbach, Eric R. Jensen, A. M. Jamieson et al. · Nature · 2001 · 1.1K citations · Full text
Life Sciences, Immunology, Oncology +14