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分子肝致癌学:炎症的影响。

Molecular hepatic carcinogenesis: impact of inflammation.

机构信息

Department of Medicine, University of Massachusetts Medical School, Worcester, USA.

出版信息

Dig Dis. 2012;30(3):243-8. doi: 10.1159/000336913. Epub 2012 Jun 20.

Abstract

Hepatocellular cancer (HCC) represents one of the most rapidly spreading cancers in the world. Most HCC develops in cirrhotic livers after prolonged inflammation, supporting the hypothesis that inflammation contributes to cancer development. Increasing evidence suggests that inflammatory cell recruitment and activation is an important contributor to promoting cancerous malformation in hepatocytes. Intracellular signaling pathways involved in classical inflammatory pathway activation can be altered in parenchymal cells, hepatocytes, in the liver to promote HCC development. Inflammation is triggered by pathogen-derived or endogenous danger-associated molecular patterns via pattern recognition receptors. Activation of the pattern recognition receptors triggers downstream signaling cascades to induce proinflammatory cytokine production, release of reactive oxygen species and modulate cellular responses. Many of these inflammatory mediators have adverse effects on DNA repair and induce DNA methylation, both of which are important elements in HCC development. This review summarizes the key points and discusses recent findings related to the role of inflammation in cancer and HCC development.

摘要

肝细胞癌 (HCC) 是世界上传播速度最快的癌症之一。大多数 HCC 在长期炎症后发生在肝硬化肝脏中,这支持了炎症有助于癌症发展的假说。越来越多的证据表明,炎症细胞募集和激活是促进肝细胞癌变的重要因素。参与经典炎症途径激活的细胞内信号通路可以在实质细胞、肝细胞中发生改变,从而促进 HCC 的发展。炎症是由病原体衍生或内源性危险相关分子模式通过模式识别受体触发的。模式识别受体的激活触发下游信号级联反应,诱导促炎细胞因子的产生、活性氧的释放,并调节细胞反应。这些炎症介质中的许多都对 DNA 修复有不良影响,并诱导 DNA 甲基化,这两者都是 HCC 发展的重要因素。本文总结了相关要点,并讨论了炎症在癌症和 HCC 发展中的作用的最新发现。

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