Saxena Mansi, Yeretssian Garabet
Department of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai , New York, NY , USA.
Department of Medicine, Immunology Institute, Icahn School of Medicine at Mount Sinai , New York, NY , USA ; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai , New York, NY , USA.
Front Immunol. 2014 Jul 14;5:327. doi: 10.3389/fimmu.2014.00327. eCollection 2014.
Cytosolic NOD-like receptors (NLRs) have been associated with human diseases including infections, cancer, and autoimmune and inflammatory disorders. These innate immune pattern recognition molecules are essential for controlling inflammatory mechanisms through induction of cytokines, chemokines, and anti-microbial genes. Upon activation, some NLRs form multi-protein complexes called inflammasomes, while others orchestrate caspase-independent nuclear factor kappa B (NF-κB) and mitogen activated protein kinase (MAPK) signaling. Moreover, NLRs and their downstream signaling components engage in an intricate crosstalk with cell death and autophagy pathways, both critical processes for cancer development. Recently, increasing evidence has extended the concept that chronic inflammation caused by abberant NLR signaling is a powerful driver of carcinogenesis, where it abets genetic mutations, tumor growth, and progression. In this review, we explore the rapidly expanding area of research regarding the expression and functions of NLRs in different types of cancers. Furthermore, we particularly focus on how maintaining tissue homeostasis and regulating tissue repair may provide a logical platform for understanding the liaisons between the NLR-driven inflammatory responses and cancer. Finally, we outline novel therapeutic approaches that target NLR signaling and speculate how these could be developed as potential pharmaceutical alternatives for cancer treatment.
胞质内的NOD样受体(NLRs)与包括感染、癌症以及自身免疫和炎症性疾病在内的人类疾病相关。这些先天性免疫模式识别分子对于通过诱导细胞因子、趋化因子和抗菌基因来控制炎症机制至关重要。激活后,一些NLRs形成称为炎性小体的多蛋白复合物,而其他NLRs则协调不依赖半胱天冬酶的核因子κB(NF-κB)和丝裂原活化蛋白激酶(MAPK)信号传导。此外,NLRs及其下游信号传导成分与细胞死亡和自噬途径进行复杂的相互作用,这两个过程对癌症发展都至关重要。最近,越来越多的证据扩展了这样的概念,即由异常NLR信号传导引起的慢性炎症是致癌作用的强大驱动力,它促进基因突变、肿瘤生长和进展。在本综述中,我们探讨了关于NLRs在不同类型癌症中的表达和功能这一迅速扩展的研究领域。此外,我们特别关注维持组织稳态和调节组织修复如何为理解NLR驱动的炎症反应与癌症之间的联系提供一个合理的平台。最后,我们概述了针对NLR信号传导的新型治疗方法,并推测这些方法如何能够发展成为癌症治疗的潜在药物替代品。