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免疫受体 NKG2D 促进肝癌模型中的肿瘤生长。

The immunoreceptor NKG2D promotes tumour growth in a model of hepatocellular carcinoma.

机构信息

Department of Life Sciences, Imperial College London, SW7 2AZ London, UK.

Department of Cellular Pathology, Imperial College London, W2 1NY London, UK.

出版信息

Nat Commun. 2017 Jan 27;8:13930. doi: 10.1038/ncomms13930.

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 CD8T 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.

摘要

炎症被认为是癌症的驱动因素之一。然而,在个别癌症中具有促肿瘤和抗肿瘤功能的个体免疫成分在很大程度上仍然未知。NKG2D 是一种有效的激活免疫受体,除了作为肿瘤抑制因子的既定功能外,它已成为炎症性疾病的重要参与者。在这里,我们提供了遗传证据,证明 NKG2D 在炎症驱动的肝癌模型中具有意外的促肿瘤作用。与 NKG2D 缺陷型小鼠相比,NKG2D 充足型小鼠表现出与肿瘤生长加速相关的特征,即记忆性 CD8T 细胞向肝脏的募集增加和促炎环境的加剧。此外,我们表明 NKG2D 有助于已知有利于肿瘤发生的肝损伤和随后的肝细胞增殖。因此,NKG2D/NKG2D 配体途径为慢性炎症与肝细胞癌的肿瘤发展之间提供了另一种机制。我们的研究结果表明,有必要有选择地针对可能受益于基于 NKG2D 的免疫疗法的癌症类型进行治疗。

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