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巨噬细胞作为癌症治疗的工具和靶点。

Macrophages as tools and targets in cancer therapy.

机构信息

Department of Biomedical Sciences, Humanitas University, Milan, Italy.

IRCCS- Humanitas Research Hospital, Milan, Italy.

出版信息

Nat Rev Drug Discov. 2022 Nov;21(11):799-820. doi: 10.1038/s41573-022-00520-5. Epub 2022 Aug 16.

Abstract

Tumour-associated macrophages are an essential component of the tumour microenvironment and have a role in the orchestration of angiogenesis, extracellular matrix remodelling, cancer cell proliferation, metastasis and immunosuppression, as well as in resistance to chemotherapeutic agents and checkpoint blockade immunotherapy. Conversely, when appropriately activated, macrophages can mediate phagocytosis of cancer cells and cytotoxic tumour killing, and engage in effective bidirectional interactions with components of the innate and adaptive immune system. Therefore, they have emerged as therapeutic targets in cancer therapy. Macrophage-targeting strategies include inhibitors of cytokines and chemokines involved in the recruitment and polarization of tumour-promoting myeloid cells as well as activators of their antitumorigenic and immunostimulating functions. Early clinical trials suggest that targeting negative regulators (checkpoints) of myeloid cell function indeed has antitumor potential. Finally, given the continuous recruitment of myelomonocytic cells into tumour tissues, macrophages are candidates for cell therapy with the development of chimeric antigen receptor effector cells. Macrophage-centred therapeutic strategies have the potential to complement, and synergize with, currently available tools in the oncology armamentarium.

摘要

肿瘤相关巨噬细胞是肿瘤微环境的重要组成部分,在血管生成、细胞外基质重塑、癌细胞增殖、转移和免疫抑制的调控中发挥作用,也在化疗药物和检查点阻断免疫治疗的耐药性中发挥作用。相反,当巨噬细胞被适当激活时,它们可以介导癌细胞的吞噬作用和细胞毒性肿瘤杀伤,并与先天和适应性免疫系统的成分进行有效的双向相互作用。因此,它们已成为癌症治疗的治疗靶点。靶向巨噬细胞的策略包括抑制细胞因子和趋化因子,这些因子参与招募和极化促进肿瘤的髓样细胞,以及激活其抗肿瘤和免疫刺激功能。早期临床试验表明,靶向髓样细胞功能的负调节剂(检查点)确实具有抗肿瘤潜力。最后,鉴于单核细胞不断募集到肿瘤组织中,巨噬细胞是嵌合抗原受体效应细胞细胞治疗的候选者。以巨噬细胞为中心的治疗策略有可能与肿瘤学武器库中现有的工具互补和协同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd9c/9380983/e2aba35b47c4/41573_2022_520_Fig1_HTML.jpg

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