• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肿瘤相关巨噬细胞免疫治疗的机制研究。

Mechanistic studies of tumor-associated macrophage immunotherapy.

机构信息

Department of Thoracic Surgery, Shenyang Chest Hospital & Tenth People's Hospital, Shenyang, Liaoning, China.

Department of Radiotherapy, The People's Hospital of Liaoning Province, Shenyang, Liaoning, China.

出版信息

Front Immunol. 2024 Sep 30;15:1476565. doi: 10.3389/fimmu.2024.1476565. eCollection 2024.

DOI:10.3389/fimmu.2024.1476565
PMID:39403370
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11472702/
Abstract

Tumor-associated macrophages (TAMs) are present in the tumor microenvironment and can polarize into subtypes with different functions and characteristics in response to different stimuli, classifying them into anti-tumorigenic M1-type and pro-tumorigenic M2-type. The M1-type macrophages inhibit tumor growth through the release of pro-inflammatory cytokines, whereas the M2-type macrophages contribute to tumor progression through the promotion of tumor proliferation, angiogenesis and metastasis. Due to the duality of macrophage effects on tumors, TAMs have been a hot topic in tumor research. In this paper, the heterogeneity and plasticity of TAMs, the interactions between TAMs and other immune cells, and the effects of TAMs on tumors are reviewed, and the therapeutic strategies for TAMs are summarized and discussed. These therapeutic strategies encompass methods and approaches to inhibit the recruitment of TAMs, deplete TAMs, and modulate the polarization of TAMs. These studies help to deeply understand the mechanism of TAMs-tumor interaction and provide reference for combination therapy of tumors.

摘要

肿瘤相关巨噬细胞(TAMs)存在于肿瘤微环境中,能够在不同刺激下极化为具有不同功能和特征的亚型,分为抗肿瘤的 M1 型和促肿瘤的 M2 型。M1 型巨噬细胞通过释放促炎细胞因子抑制肿瘤生长,而 M2 型巨噬细胞通过促进肿瘤增殖、血管生成和转移促进肿瘤进展。由于巨噬细胞对肿瘤的影响具有双重性,TAMs 一直是肿瘤研究的热点。本文综述了 TAMs 的异质性和可塑性、TAMs 与其他免疫细胞的相互作用以及 TAMs 对肿瘤的影响,并对 TAMs 的治疗策略进行了总结和讨论。这些治疗策略包括抑制 TAMs 募集、耗竭 TAMs 以及调节 TAMs 极化的方法和途径。这些研究有助于深入理解 TAMs-肿瘤相互作用的机制,并为肿瘤的联合治疗提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/eb967f1aaefd/fimmu-15-1476565-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/503e469bcb8c/fimmu-15-1476565-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/8cae3e96ad5f/fimmu-15-1476565-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/eb967f1aaefd/fimmu-15-1476565-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/503e469bcb8c/fimmu-15-1476565-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/8cae3e96ad5f/fimmu-15-1476565-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f99a/11472702/eb967f1aaefd/fimmu-15-1476565-g003.jpg

相似文献

1
Mechanistic studies of tumor-associated macrophage immunotherapy.肿瘤相关巨噬细胞免疫治疗的机制研究。
Front Immunol. 2024 Sep 30;15:1476565. doi: 10.3389/fimmu.2024.1476565. eCollection 2024.
2
Deciphering the performance of macrophages in tumour microenvironment: a call for precision immunotherapy.解析肿瘤微环境中巨噬细胞的功能:对精准免疫治疗的呼唤。
J Hematol Oncol. 2024 Jun 11;17(1):44. doi: 10.1186/s13045-024-01559-0.
3
Macrophage polarization in the tumor microenvironment: Emerging roles and therapeutic potentials.肿瘤微环境中的巨噬细胞极化:新兴作用和治疗潜力。
Biomed Pharmacother. 2024 Aug;177:116930. doi: 10.1016/j.biopha.2024.116930. Epub 2024 Jun 14.
4
An update to experimental and clinical aspects of tumor-associated macrophages in cancer development: hopes and pitfalls.肿瘤相关巨噬细胞在癌症发展中的实验和临床研究进展:希望与陷阱。
Clin Exp Med. 2024 Jul 13;24(1):156. doi: 10.1007/s10238-024-01417-w.
5
Macrophage-based cancer immunotherapy: Challenges and opportunities.基于巨噬细胞的癌症免疫疗法:挑战与机遇。
Exp Cell Res. 2024 Sep 1;442(1):114198. doi: 10.1016/j.yexcr.2024.114198. Epub 2024 Aug 3.
6
Tumor microenvironment remodeling and tumor therapy based on M2-like tumor associated macrophage-targeting nano-complexes.基于 M2 样肿瘤相关巨噬细胞靶向纳米复合物的肿瘤微环境重塑与肿瘤治疗。
Theranostics. 2021 Jan 1;11(6):2892-2916. doi: 10.7150/thno.50928. eCollection 2021.
7
Shaping Polarization Of Tumor-Associated Macrophages In Cancer Immunotherapy.塑造肿瘤相关巨噬细胞在癌症免疫治疗中的极化。
Front Immunol. 2022 Jun 30;13:888713. doi: 10.3389/fimmu.2022.888713. eCollection 2022.
8
Targeting tumor-associated macrophages: A potential treatment for solid tumors.靶向肿瘤相关巨噬细胞:实体瘤的一种潜在治疗方法。
J Cell Physiol. 2021 May;236(5):3445-3465. doi: 10.1002/jcp.30139. Epub 2020 Nov 16.
9
Molecular understanding and clinical aspects of tumor-associated macrophages in the immunotherapy of renal cell carcinoma.肿瘤相关巨噬细胞在肾细胞癌免疫治疗中的分子认识和临床方面。
J Exp Clin Cancer Res. 2024 Aug 22;43(1):242. doi: 10.1186/s13046-024-03164-y.
10
Tumor-associated macrophages: A promising target for a cancer immunotherapeutic strategy.肿瘤相关巨噬细胞:癌症免疫治疗策略的有前途的靶点。
Pharmacol Res. 2020 Nov;161:105111. doi: 10.1016/j.phrs.2020.105111. Epub 2020 Oct 13.

引用本文的文献

1
ESR1 Expression Negatively Correlates with Immune Cell Infiltration and Response to Immune Checkpoint Inhibitors in Estrogen Receptor-Positive/HER2-Negative Breast Cancer.ESR1表达与雌激素受体阳性/人表皮生长因子受体2阴性乳腺癌中的免疫细胞浸润及免疫检查点抑制剂反应呈负相关。
Ann Surg Oncol. 2025 Sep 16. doi: 10.1245/s10434-025-18260-2.
2
Machine learning model in multi-omics perspective demystifies the prognostic significance of crotonylation heterogeneity in clear cell renal cell carcinoma.多组学视角下的机器学习模型揭示了透明细胞肾细胞癌中巴豆酰化异质性的预后意义。
BMC Urol. 2025 Sep 15;25(1):229. doi: 10.1186/s12894-025-01914-4.
3

本文引用的文献

1
Deciphering the performance of macrophages in tumour microenvironment: a call for precision immunotherapy.解析肿瘤微环境中巨噬细胞的功能:对精准免疫治疗的呼唤。
J Hematol Oncol. 2024 Jun 11;17(1):44. doi: 10.1186/s13045-024-01559-0.
2
Engineered CD47 protects T cells for enhanced antitumour immunity.工程化 CD47 保护 T 细胞以增强抗肿瘤免疫。
Nature. 2024 Jun;630(8016):457-465. doi: 10.1038/s41586-024-07443-8. Epub 2024 May 15.
3
Bacterial protoplast-derived nanovesicles carrying CRISPR-Cas9 tools re-educate tumor-associated macrophages for enhanced cancer immunotherapy.
Polarization of Tumor Cells and Tumor-Associated Macrophages: Molecular Mechanisms and Therapeutic Targets.
肿瘤细胞与肿瘤相关巨噬细胞的极化:分子机制与治疗靶点
MedComm (2020). 2025 Sep 1;6(9):e70372. doi: 10.1002/mco2.70372. eCollection 2025 Sep.
4
Exploring the Causal Effect of Mitochondrial DNA Copy Number on Obstructive Sleep Apnea.探索线粒体DNA拷贝数对阻塞性睡眠呼吸暂停的因果效应。
Brain Behav. 2025 Aug;15(8):e70720. doi: 10.1002/brb3.70720.
5
A multifunctional biomimetic nanoplatform combined with immune checkpoint blockade for triple-negative breast cancer immunotherapy through inhibiting polarization of M2 macrophages.一种多功能仿生纳米平台,通过抑制M2巨噬细胞极化,联合免疫检查点阻断用于三阴性乳腺癌免疫治疗。
J Nanobiotechnology. 2025 Aug 18;23(1):569. doi: 10.1186/s12951-025-03663-w.
6
Biomimetic tumor cell membrane-camouflaged nanomicelles for synergistic chemo-immunotherapy of Triple-negative breast cancer.用于三阴性乳腺癌协同化学免疫治疗的仿生肿瘤细胞膜伪装纳米胶束
Mater Today Bio. 2025 Jun 25;33:102012. doi: 10.1016/j.mtbio.2025.102012. eCollection 2025 Aug.
7
Traditional Chinese medicine in the prevention and treatment of lung cancer metastasis by regulating tumor-associated macrophages: a narrative review.传统中医通过调节肿瘤相关巨噬细胞预防和治疗肺癌转移:一项叙述性综述
Transl Lung Cancer Res. 2025 Jun 30;14(6):2281-2295. doi: 10.21037/tlcr-2025-380. Epub 2025 Jun 26.
8
Oxidized Low-Density Lipoprotein as a Potential Target for Enhancing Immune Checkpoint Inhibitor Therapy in Microsatellite-Stable Colorectal Cancer.氧化型低密度脂蛋白作为增强微卫星稳定型结直肠癌免疫检查点抑制剂治疗的潜在靶点
Antioxidants (Basel). 2025 Jun 13;14(6):726. doi: 10.3390/antiox14060726.
9
Cytokine release syndrome and CAR T Cell therapy: Modulating the intensity of the inflammatory response and resolution within the tumor microenvironment.细胞因子释放综合征与嵌合抗原受体T细胞疗法:调节肿瘤微环境中炎症反应的强度及消退
Front Pharmacol. 2025 Jun 10;16:1615526. doi: 10.3389/fphar.2025.1615526. eCollection 2025.
10
Unraveling the role of M2 TAMs in ovarian cancer dynamics: a systematic review.解析M2肿瘤相关巨噬细胞在卵巢癌动态变化中的作用:一项系统综述
J Transl Med. 2025 Jun 3;23(1):623. doi: 10.1186/s12967-025-06643-8.
细菌原生质体衍生的纳米囊泡携带 CRISPR-Cas9 工具,重新教育肿瘤相关巨噬细胞,增强癌症免疫治疗。
Nat Commun. 2024 Jan 31;15(1):950. doi: 10.1038/s41467-024-44941-9.
4
The promising role of tumor-associated macrophages in the treatment of cancer.肿瘤相关巨噬细胞在癌症治疗中的前景作用。
Drug Resist Updat. 2024 Mar;73:101041. doi: 10.1016/j.drup.2023.101041. Epub 2024 Jan 3.
5
Blockade of tumor-derived colony-stimulating factor 1 (CSF1) promotes an immune-permissive tumor microenvironment.阻断肿瘤来源的集落刺激因子 1(CSF1)可促进免疫许可的肿瘤微环境。
Cancer Immunol Immunother. 2023 Oct;72(10):3349-3362. doi: 10.1007/s00262-023-03496-2. Epub 2023 Jul 28.
6
TRAF3/STAT6 axis regulates macrophage polarization and tumor progression.TRAF3/STAT6 轴调节巨噬细胞极化和肿瘤进展。
Cell Death Differ. 2023 Aug;30(8):2005-2016. doi: 10.1038/s41418-023-01194-1. Epub 2023 Jul 21.
7
Smoking-Induced M2-TAMs, via circEML4 in EVs, Promote the Progression of NSCLC through ALKBH5-Regulated m6A Modification of SOCS2 in NSCLC Cells.香烟诱导的 M2-TAMs 通过 EV 中的 circEML4 促进 NSCLC 的进展,通过 NSCLC 细胞中 SOCS2 的 ALKBH5 调控的 m6A 修饰促进 NSCLC 的进展。
Adv Sci (Weinh). 2023 Aug;10(22):e2300953. doi: 10.1002/advs.202300953. Epub 2023 May 28.
8
Precision Killing of M2 Macrophages with Phage-Displayed Peptide-Photosensitizer Conjugates.利用噬菌体展示肽-光敏剂偶联物精准杀伤M2巨噬细胞
Cancers (Basel). 2023 Mar 28;15(7):2009. doi: 10.3390/cancers15072009.
9
Lipid metabolism reprogramming in tumor-associated macrophages and implications for therapy.肿瘤相关巨噬细胞中的脂质代谢重编程及其治疗意义。
Lipids Health Dis. 2023 Mar 31;22(1):45. doi: 10.1186/s12944-023-01807-1.
10
Necroptosis of macrophage is a key pathological feature in biliary atresia via GDCA/S1PR2/ZBP1/p-MLKL axis.巨噬细胞的坏死是通过 GDCA/S1PR2/ZBP1/p-MLKL 轴在胆道闭锁中的一个关键的病理特征。
Cell Death Dis. 2023 Mar 1;14(3):175. doi: 10.1038/s41419-023-05615-4.