• 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

巨噬细胞在不同肿瘤微环境中的独特作用。

Distinct role of macrophages in different tumor microenvironments.

作者信息

Lewis Claire E, Pollard Jeffrey W

机构信息

Academic Unit of Pathology, Division of Genomic Medicine, University of Sheffield Medical School, Beech Hill Road, Sheffield S10 2RX, United Kingdom.

出版信息

Cancer Res. 2006 Jan 15;66(2):605-12. doi: 10.1158/0008-5472.CAN-05-4005.

DOI:10.1158/0008-5472.CAN-05-4005
PMID:16423985
Abstract

Macrophages are prominent in the stromal compartment of virtually all types of malignancy. These highly versatile cells respond to the presence of stimuli in different parts of tumors with the release of a distinct repertoire of growth factors, cytokines, chemokines, and enzymes that regulate tumor growth, angiogenesis, invasion, and/or metastasis. The distinct microenvironments where tumor-associated macrophages (TAM) act include areas of invasion where TAMs promote cancer cell motility, stromal and perivascular areas where TAMs promote metastasis, and avascular and perinecrotic areas where hypoxic TAMs stimulate angiogenesis. This review will discuss the evidence for differential regulation of TAMs in these microenvironments and provide an overview of current attempts to target or use TAMs for therapeutic purposes.

摘要

巨噬细胞在几乎所有类型恶性肿瘤的基质区室中都很突出。这些高度多功能的细胞对肿瘤不同部位的刺激作出反应,释放出一系列独特的生长因子、细胞因子、趋化因子和酶,从而调节肿瘤生长、血管生成、侵袭和/或转移。肿瘤相关巨噬细胞(TAM)发挥作用的不同微环境包括TAM促进癌细胞运动的侵袭区域、TAM促进转移的基质和血管周围区域,以及缺氧TAM刺激血管生成的无血管和坏死周围区域。本综述将讨论这些微环境中TAM差异调节的证据,并概述目前针对TAM或利用TAM进行治疗的尝试。

相似文献

1
Distinct role of macrophages in different tumor microenvironments.巨噬细胞在不同肿瘤微环境中的独特作用。
Cancer Res. 2006 Jan 15;66(2):605-12. doi: 10.1158/0008-5472.CAN-05-4005.
2
Tumor-associated macrophages: role in cancer development and therapeutic implications.肿瘤相关巨噬细胞:在癌症发展中的作用及治疗意义。
Cell Oncol (Dordr). 2019 Oct;42(5):591-608. doi: 10.1007/s13402-019-00453-z. Epub 2019 May 29.
3
Tumor versus tumor-associated macrophages: how hot is the link?肿瘤与肿瘤相关巨噬细胞:二者联系有多紧密?
Integr Cancer Ther. 2008 Jun;7(2):90-5. doi: 10.1177/1534735408319060.
4
The roles of tumor-associated macrophages in tumor angiogenesis and metastasis.肿瘤相关巨噬细胞在肿瘤血管生成和转移中的作用。
Cell Immunol. 2020 Jul;353:104119. doi: 10.1016/j.cellimm.2020.104119. Epub 2020 May 4.
5
Differential macrophage programming in the tumor microenvironment.肿瘤微环境中的巨噬细胞差异化编程。
Trends Immunol. 2012 Mar;33(3):119-26. doi: 10.1016/j.it.2011.12.001. Epub 2012 Jan 23.
6
New Mechanisms of Tumor-Associated Macrophages on Promoting Tumor Progression: Recent Research Advances and Potential Targets for Tumor Immunotherapy.肿瘤相关巨噬细胞促进肿瘤进展的新机制:肿瘤免疫治疗的最新研究进展和潜在靶点。
J Immunol Res. 2016;2016:9720912. doi: 10.1155/2016/9720912. Epub 2016 Nov 16.
7
Tumor-associated macrophages: effectors of angiogenesis and tumor progression.肿瘤相关巨噬细胞:血管生成和肿瘤进展的效应细胞
Biochim Biophys Acta. 2009 Aug;1796(1):11-8. doi: 10.1016/j.bbcan.2009.02.004. Epub 2009 Mar 6.
8
The Role of Tumor Associated Macrophages (TAMs) in Cancer Progression, Chemoresistance, Angiogenesis and Metastasis - Current Status.肿瘤相关巨噬细胞(TAMs)在癌症进展、化疗耐药性、血管生成和转移中的作用——现状。
Curr Med Chem. 2021;28(39):8203-8236. doi: 10.2174/0929867328666210720143721.
9
Tumor-Associated Macrophages as Target for Antitumor Therapy.肿瘤相关巨噬细胞作为抗肿瘤治疗的靶点。
Arch Immunol Ther Exp (Warsz). 2018 Apr;66(2):97-111. doi: 10.1007/s00005-017-0480-8. Epub 2017 Jun 28.
10
Macrophage regulation of tumor responses to anticancer therapies.肿瘤对抗癌疗法反应的巨噬细胞调控。
Cancer Cell. 2013 Mar 18;23(3):277-86. doi: 10.1016/j.ccr.2013.02.013.

引用本文的文献

1
The Impact of Proinflammatory M1 Macrophages on the Proliferation and Expression of Cyclin E2, Mitogen-Activated Protein Kinases 4 and 7 in Hepatocytes Isolated from a Diethylnitrosamine-Induced Hepatocellular Carcinoma Rat Model.促炎M1巨噬细胞对二乙基亚硝胺诱导的肝癌大鼠模型分离的肝细胞中细胞周期蛋白E2、丝裂原活化蛋白激酶4和7的增殖及表达的影响
Molecules. 2025 Sep 8;30(17):3657. doi: 10.3390/molecules30173657.
2
CD68 as a multi-omic prognostic biomarker in digestive system cancers: correlations with tumor-infiltrating immune cells and immune checkpoints.CD68作为消化系统癌症的多组学预后生物标志物:与肿瘤浸润免疫细胞和免疫检查点的相关性
Front Immunol. 2025 Aug 21;16:1599677. doi: 10.3389/fimmu.2025.1599677. eCollection 2025.
3
Locally Reprogramming Tumor-Associated Macrophages with Cytokine-Loaded Injectable Cryogels for Breast Cancer.
利用负载细胞因子的可注射冷冻凝胶对乳腺癌相关巨噬细胞进行局部重编程
Ann Biomed Eng. 2025 Aug 29. doi: 10.1007/s10439-025-03823-x.
4
Lymph node transcriptomic profiles suggest susceptibility to bleomycin-induced pulmonary toxicity in classic hodgkin lymphoma.淋巴结转录组图谱提示经典型霍奇金淋巴瘤对博来霉素诱导的肺毒性易感。
Sci Rep. 2025 Aug 18;15(1):30273. doi: 10.1038/s41598-025-16218-8.
5
Tumor-associated macrophages: potential role in skeletal involvement in classic Hodgkin lymphoma.肿瘤相关巨噬细胞:在经典型霍奇金淋巴瘤骨骼受累中的潜在作用
J Pathol Clin Res. 2025 Jul;11(4):e70038. doi: 10.1002/2056-4538.70038.
6
Immunomodulatory effects of photothermal therapy in breast cancer: advances and challenges.光热疗法在乳腺癌中的免疫调节作用:进展与挑战
Front Immunol. 2025 Jul 4;16:1544693. doi: 10.3389/fimmu.2025.1544693. eCollection 2025.
7
Metastatic heterogeneity in pancreatic cancer: mechanisms and opportunities for targeted intervention.胰腺癌的转移异质性:靶向干预的机制与机遇
J Clin Invest. 2025 Jul 15;135(14). doi: 10.1172/JCI191943.
8
Molecular Mechanisms of Lymphatic Metastasis in Breast Cancer: An Updated Review.乳腺癌淋巴转移的分子机制:最新综述
Cancers (Basel). 2025 Jun 25;17(13):2134. doi: 10.3390/cancers17132134.
9
Tumor microenvironment in osteosarcoma: From cellular mechanism to clinical therapy.骨肉瘤中的肿瘤微环境:从细胞机制到临床治疗
Genes Dis. 2025 Feb 20;12(5):101569. doi: 10.1016/j.gendis.2025.101569. eCollection 2025 Sep.
10
An improved reference library and method for accurate cell-type deconvolution of bulk-tissue miRNA data.一种用于批量组织miRNA数据精确细胞类型反卷积的改进参考文库和方法。
Nat Commun. 2025 Jul 1;16(1):5508. doi: 10.1038/s41467-025-60521-x.