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炎症与癌症:miRNA、自由基、细胞因子与 p53 通路的交织。

Inflammation and cancer: interweaving microRNA, free radical, cytokine and p53 pathways.

机构信息

Laboratory of Human Carcinogenesis, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Carcinogenesis. 2010 Jan;31(1):37-49. doi: 10.1093/carcin/bgp272. Epub 2009 Dec 2.

Abstract

Chronic inflammation and infection are major causes of cancer. There are continued improvements to our understanding of the molecular connections between inflammation and cancer. Key mediators of inflammation-induced cancer include nuclear factor kappa B, reactive oxygen and nitrogen species, inflammatory cytokines, prostaglandins and specific microRNAs. The collective activity of these mediators is largely responsible for either a pro-tumorigenic or anti-tumorigenic inflammatory response through changes in cell proliferation, cell death, cellular senescence, DNA mutation rates, DNA methylation and angiogenesis. As our understanding grows, inflammatory mediators will provide opportunities to develop novel diagnostic and therapeutic strategies. In this review, we provide a general overview of the connection between inflammation, microRNAs and cancer and highlight how our improved understanding of these connections may provide novel preventive, diagnostic and therapeutic strategies to reduce the health burden of cancer.

摘要

慢性炎症和感染是癌症的主要原因。我们对炎症和癌症之间的分子联系的理解在不断提高。炎症诱导癌症的关键介质包括核因子 kappa B、活性氧和氮物种、炎症细胞因子、前列腺素和特定的 microRNAs。这些介质的集体活动主要通过改变细胞增殖、细胞死亡、细胞衰老、DNA 突变率、DNA 甲基化和血管生成来导致促肿瘤或抗肿瘤炎症反应。随着我们的理解不断深入,炎症介质将为开发新的诊断和治疗策略提供机会。在这篇综述中,我们提供了炎症、microRNAs 和癌症之间联系的概述,并强调了我们对这些联系的理解如何为减少癌症的健康负担提供新的预防、诊断和治疗策略。

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