Division of Hepatobiliary and Pancreatic Surgery, Department of Surgery, State University of New York Upstate Medical University , Albany, NY , USA.
Department of Microbiology and Immunology, University of Maryland School of Medicine , Baltimore, MD , USA.
Front Immunol. 2014 Nov 17;5:553. doi: 10.3389/fimmu.2014.00553. eCollection 2014.
Chronic inflammation has long been associated with the development of cancer. Among the various signaling pathways within cancer cells that can incite the expression of inflammatory molecules are those that activate IL-1 receptor-associated kinases (IRAK). The IRAK family is comprised of four family members, IRAK-1, IRAK-2, IRAK-3 (also known as IRAK-M), and IRAK-4, which play important roles in both positively and negatively regulating the expression of inflammatory molecules. The wide array of inflammatory molecules that are expressed in response to IRAK signaling within the tumor microenvironment regulate the production of factors which promote tumor growth, metastasis, immune suppression, and chemotherapy resistance. Based on published reports we propose that dysregulated activation of the IRAK signaling pathway in cancer cells contributes to disease progression by creating a highly inflammatory tumor environment. In this article, we present both theoretical arguments and reference experimental data in support of this hypothesis.
慢性炎症长期以来一直与癌症的发展有关。在能够引发炎症分子表达的癌细胞内的各种信号通路中,有那些激活白细胞介素 1 受体相关激酶 (IRAK) 的通路。IRAK 家族由四个家族成员组成,IRAK-1、IRAK-2、IRAK-3(也称为 IRAK-M)和 IRAK-4,它们在正向和负向调节炎症分子的表达中都起着重要作用。在肿瘤微环境中 IRAK 信号诱导表达的广泛的炎症分子调节促进肿瘤生长、转移、免疫抑制和化疗耐药的因子的产生。基于已发表的报告,我们提出癌细胞中 IRAK 信号通路的失调激活通过创造高度炎症的肿瘤环境促进疾病进展。在本文中,我们提出了理论论据和参考实验数据来支持这一假设。