Inflammation Biology Group, Centre d'Immunologie Marseille-Luminy, Marseille, France.
Clin Cancer Res. 2010 Feb 1;16(3):784-9. doi: 10.1158/1078-0432.CCR-09-1015. Epub 2010 Jan 26.
Tumor-associated macrophages (TAM) have been linked with the progression of cancer by favoring tumor angiogenesis, growth, and metastasis. The precise mechanisms that maintain the protumor phenotype of TAM are poorly understood, but recent research has highlighted a number of signaling pathways that are important in TAM phenotype and function. Nuclear factor-kappaB (NF-kappaB) is considered the master regulator of inflammatory and immune responses. Recently several genetic studies have indicated NF-kappaB is an important pathway in TAM for the integration of signals from the tumor microenvironment that promote carcinogenesis. This review will focus on the role of NF-kappaB in TAM and the potential of targeting this pathway as a novel therapeutic strategy against cancer.
肿瘤相关巨噬细胞(TAM)通过促进肿瘤血管生成、生长和转移与癌症的进展有关。维持 TAM 促肿瘤表型的确切机制尚不清楚,但最近的研究强调了许多在 TAM 表型和功能中起重要作用的信号通路。核因子-κB(NF-κB)被认为是炎症和免疫反应的主要调节剂。最近的几项遗传研究表明,NF-κB 是 TAM 中整合来自肿瘤微环境促进癌变信号的重要途径。本文综述了 NF-κB 在 TAM 中的作用以及将该途径作为一种新的癌症治疗策略的潜力。