Singh Saroj, Mehta Neesha, Lilan Jiang, Budhthoki Meen Bahadur, Chao Fu, Yong Li
Department of Oral and Maxillofacial Surgery, The Affiliated Hospital of Stomatology, Chongqing Medical University, No. 426 Songshibei Road, Yubei District, Chongqing 401147, China.
Biochim Open. 2017 Jan 5;4:8-18. doi: 10.1016/j.biopen.2016.11.002. eCollection 2017 Jun.
Tumor-associated macrophages (TAMs) are a significant component of the microenvironment of any solid tumors in the majority of cancers, associated with unfavorable prognosis. TAMs emerge as attractive targets for therapeutic strategies aimed at reprogramming their protumor phenotype into an effective antitumor activity. In this review article, we present an overview of mechanisms responsible for TAMs recruitment and highlight the roles of TAMs in the regulation of tumor angiogenesis, invasion, metastasis, immunosuppression, and chemotherapeutic resistance. We describe the interplay between Th17 cells and other immune cells in the tumor microenvironment, and we assess both the potential antitumorigenic and pro-tumorigenic activities of Th17 cells and their associated cytokines. Understanding the nature of Th17 cell responses in the tumor microenvironment will be important for the design of more efficacious cancer immunotherapies. Finally, we discuss TAM-targeting therapy as a promising novel strategy for an indirect cancer therapy.
肿瘤相关巨噬细胞(TAMs)是大多数癌症中任何实体瘤微环境的重要组成部分,与不良预后相关。TAMs成为旨在将其促肿瘤表型重编程为有效抗肿瘤活性的治疗策略的有吸引力的靶点。在这篇综述文章中,我们概述了负责TAMs募集的机制,并强调了TAMs在肿瘤血管生成、侵袭、转移、免疫抑制和化疗耐药性调节中的作用。我们描述了肿瘤微环境中Th17细胞与其他免疫细胞之间的相互作用,并评估了Th17细胞及其相关细胞因子的潜在抗肿瘤和促肿瘤活性。了解肿瘤微环境中Th17细胞反应的本质对于设计更有效的癌症免疫疗法至关重要。最后,我们讨论了靶向TAM疗法作为一种有前景的间接癌症治疗新策略。