Department of Gastrointestinal Surgery, Tongji Medical College, Union Hospital, Huazhong University of Science and Technology, Wuhan 430022, China.
Curr Oncol. 2024 Nov 17;31(11):7275-7286. doi: 10.3390/curroncol31110536.
Immunotherapy, particularly immune checkpoint inhibitors like PD-1, PD-L1, and CTLA-4, has revolutionized cancer treatment. However, the role of the innate immune system, especially pattern recognition receptors, in cancer development and immunity is gaining more and more attention. Dectin-1, a C-type lectin receptor primarily involved in antifungal immunity, has emerged as a significant player in cancer biology, exhibiting both pro-tumor and anti-tumor roles. This dual function largely depends on the tumor type and microenvironment. Dectin-1 can promote immune responses against tumors like melanoma and breast cancer by enhancing both innate and adaptive immunity. However, in tumors like pancreatic ductal adenocarcinoma and colorectal cancer, Dectin-1 activation suppresses T cell immunity, facilitating tumor progression. This review explores the complex mechanisms by which Dectin-1 modulates the tumor microenvironment and discusses its potential as a therapeutic target for cancer treatment.
免疫疗法,特别是免疫检查点抑制剂如 PD-1、PD-L1 和 CTLA-4,已经彻底改变了癌症治疗。然而,先天免疫系统,特别是模式识别受体在癌症发展和免疫中的作用越来越受到关注。Dectin-1 是一种主要参与抗真菌免疫的 C 型凝集素受体,已成为癌症生物学中的重要角色,表现出促肿瘤和抗肿瘤作用。这种双重功能在很大程度上取决于肿瘤类型和微环境。Dectin-1 通过增强先天和适应性免疫来促进对黑色素瘤和乳腺癌等肿瘤的免疫反应。然而,在胰腺导管腺癌和结直肠癌等肿瘤中,Dectin-1 的激活抑制了 T 细胞免疫,促进了肿瘤的进展。本综述探讨了 Dectin-1 调节肿瘤微环境的复杂机制,并讨论了其作为癌症治疗的治疗靶点的潜力。