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系统性炎症反应作为肝细胞癌生物标志物和治疗靶点的来源。

The systemic inflammatory response as a source of biomarkers and therapeutic targets in hepatocellular carcinoma.

机构信息

Department of Medicine, Imperial College London, London, UK.

Department of Surgery and Cancer, Imperial College London, Hammersmith Hospital, London, UK.

出版信息

Liver Int. 2019 Nov;39(11):2008-2023. doi: 10.1111/liv.14220. Epub 2019 Sep 18.

Abstract

The pathogenesis of hepatocellular carcinoma (HCC) strongly relates to inflammation, with chronic up-regulation of pro-inflammatory mediators standing as a potential unifying mechanism that underscores the origin and progression of HCC independent of aetiology. Activation of the diverse pro-inflammatory mediators either within the tumour or its microenvironment is part of an active cross-talk between the progressive HCC and the host, which is known to influence clinical outcomes including recurrence after radical treatments and long-term survival. A number of clinical biomarkers to measure the severity of cancer-related inflammation are now available, most of which emerge from routine blood parameters including neutrophil, lymphocyte, platelet counts, as well as albuminaemia and C-reactive protein levels. In this review, we summarise the body of evidence supporting the biologic qualification of inflammation-based scores in HCC and review their potential in facilitating the prognostic assessment and treatment allocation in the individual patient. We also discuss the evidence to suggest modulation of tumour-promoting inflammation may act as a source of novel therapeutic strategies in liver cancer.

摘要

肝细胞癌 (HCC) 的发病机制与炎症密切相关,慢性上调促炎介质被认为是一种潜在的统一机制,强调了 HCC 的起源和进展与病因无关。肿瘤或其微环境中各种促炎介质的激活是进行性 HCC 与宿主之间积极相互作用的一部分,已知这会影响临床结果,包括根治性治疗后的复发和长期生存。目前有许多用于衡量与癌症相关炎症严重程度的临床生物标志物,其中大多数来自常规血液参数,包括中性粒细胞、淋巴细胞、血小板计数以及白蛋白和 C 反应蛋白水平。在这篇综述中,我们总结了支持基于炎症的 HCC 评分的生物学证据,并回顾了它们在个体患者的预后评估和治疗分配中的潜在应用。我们还讨论了一些证据,表明抑制肿瘤促进炎症可能成为肝癌新的治疗策略的来源。

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