癌症研究
血管生成
肿瘤微环境
转移
巨噬细胞
重编程
免疫抑制
医学
免疫疗法
生物
癌症
免疫系统
细胞
免疫学
肿瘤细胞
内科学
体外
生物化学
遗传学
作者
Yibing Chen,Shengkan Jin,Yucen Song,Ting Huang,Jun Cao,Qing Tang,Zhengzhi Zou
摘要
Abstract Tumor‐associated macrophages (TAMs) in solid tumors exert protumor activities by releasing cytokines or growth factors into the tumor microenvironment. Increasing studies have also shown that TAMs play a key role in tumor progression, such as tumor angiogenesis, immunosuppression, cell proliferation, migration, invasion, and metastasis. A large body of evidence shows that the abundance of TAMs in solid tumors is correlated with poor disease prognosis and resistance to therapies. Therefore, targeting TAMs in solid tumors is considered to be a promising immunotherapeutic strategy. At present, the therapeutic strategies of targeting macrophages mainly include limiting monocyte recruitment, depletion strategies, promoting macrophage phagocytic activity, and induction of macrophage reprogramming. Additionally, targeting TAMs in combination with conventional therapies has been demonstrated to be a promising therapeutic strategy in solid tumors. In the present review, we summarized various TAMs‐targeting therapeutic strategies for treating solid tumors. This review also discusses the challenges for targeting TAMs as tumor treatments, the obstacles in clinical trials, and the perspective for the future development of TAMs‐targeting therapies for various cancers.
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