• 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

相似文献

1
Regulation of tumor metastasis by myeloid-derived suppressor cells.髓源性抑制细胞对肿瘤转移的调控
Annu Rev Med. 2015;66:97-110. doi: 10.1146/annurev-med-051013-052304. Epub 2014 Oct 9.
2
Transcriptional regulation of myeloid-derived suppressor cells.髓源性抑制细胞的转录调控
J Leukoc Biol. 2015 Dec;98(6):913-22. doi: 10.1189/jlb.4RI0515-204R. Epub 2015 Sep 3.
3
Contribution of myeloid-derived suppressor cells to tumor-induced immune suppression, angiogenesis, invasion and metastasis.髓系来源的抑制细胞对肿瘤诱导的免疫抑制、血管生成、浸润和转移的贡献。
J Genet Genomics. 2010 Jul;37(7):423-30. doi: 10.1016/S1673-8527(09)60061-8.
4
In Brief: Myeloid-derived suppressor cells in cancer.简而言之:癌症中的髓源性抑制细胞。
J Pathol. 2017 May;242(1):7-9. doi: 10.1002/path.4876. Epub 2017 Mar 21.
5
Myeloid-Derived Suppressor Cells: Critical Cells Driving Immune Suppression in the Tumor Microenvironment.髓源性抑制细胞:肿瘤微环境中驱动免疫抑制的关键细胞
Adv Cancer Res. 2015;128:95-139. doi: 10.1016/bs.acr.2015.04.002. Epub 2015 May 12.
6
Myeloid-derived suppressor cells: Important contributors to tumor progression and metastasis.髓源性抑制细胞:肿瘤进展和转移的重要贡献者。
J Cell Physiol. 2018 Apr;233(4):3024-3036. doi: 10.1002/jcp.26075. Epub 2017 Aug 3.
7
Roles of Myeloid-Derived Suppressor Cells in Cancer Metastasis: Immunosuppression and Beyond.髓系来源的抑制细胞在癌症转移中的作用:免疫抑制及其他。
Arch Immunol Ther Exp (Warsz). 2019 Apr;67(2):89-102. doi: 10.1007/s00005-018-0531-9. Epub 2018 Nov 2.
8
Myeloid Derived Suppressor Cells Interactions With Natural Killer Cells and Pro-angiogenic Activities: Roles in Tumor Progression.髓源性抑制细胞与自然杀伤细胞的相互作用及其促血管生成活性:在肿瘤进展中的作用。
Front Immunol. 2019 Apr 18;10:771. doi: 10.3389/fimmu.2019.00771. eCollection 2019.
9
Intertwined regulation of angiogenesis and immunity by myeloid cells.髓系细胞对血管生成和免疫的相互调节
Trends Immunol. 2015 Apr;36(4):240-9. doi: 10.1016/j.it.2015.02.005. Epub 2015 Mar 11.
10
The metastasis-promoting roles of tumor-associated immune cells.肿瘤相关免疫细胞的促转移作用。
J Mol Med (Berl). 2013 Apr;91(4):411-29. doi: 10.1007/s00109-013-1021-5. Epub 2013 Mar 21.

引用本文的文献

1
Cancer Immunotherapy in Combination with Radiotherapy and/or Chemotherapy: Mechanisms and Clinical Therapy.癌症免疫疗法与放疗和/或化疗联合应用:作用机制与临床治疗
MedComm (2020). 2025 Aug 31;6(9):e70346. doi: 10.1002/mco2.70346. eCollection 2025 Sep.
2
The role of exosomes in bladder cancer immunotherapy.外泌体在膀胱癌免疫治疗中的作用。
J Natl Cancer Cent. 2025 May 2;5(3):252-266. doi: 10.1016/j.jncc.2025.04.001. eCollection 2025 Jun.
3
SENP1: A perspective from immune cells to disease (Review).SENP1:从免疫细胞到疾病的视角(综述)。
Oncol Rep. 2025 Sep;54(3). doi: 10.3892/or.2025.8947. Epub 2025 Jul 19.
4
Metastasis-promoting functions of myeloid cells.髓系细胞的促转移功能。
Cancer Metastasis Rev. 2025 Jul 15;44(3):61. doi: 10.1007/s10555-025-10278-y.
5
Different neutrophil extracellular trap related Ewing sarcoma subtypes exhibit distinct prognosis, and immune microenvironment characteristics.不同的中性粒细胞胞外诱捕网相关尤文肉瘤亚型表现出不同的预后和免疫微环境特征。
Sci Rep. 2025 Jul 8;15(1):24523. doi: 10.1038/s41598-025-10277-7.
6
Myeloid-derived suppressor cells modulation in the context of tumor microenvironment for gastric cancer.胃癌肿瘤微环境背景下髓源性抑制细胞的调控
Clin Transl Oncol. 2025 Jun 24. doi: 10.1007/s12094-025-03960-8.
7
Alternative splicing of KLF4 in myeloid cells: implications for cellular plasticity and trained immunity in cancer and inflammatory disease.髓系细胞中KLF4的可变剪接:对癌症和炎症性疾病中细胞可塑性和训练免疫的影响
Front Immunol. 2025 Jun 9;16:1585528. doi: 10.3389/fimmu.2025.1585528. eCollection 2025.
8
Comprehensive pan-cancer analysis and experimental validation reveal FCHSD1 as a potential biomarker for diagnosis, immune infiltration, and prognosis.全面的泛癌分析和实验验证表明,FCHSD1是一种用于诊断、免疫浸润和预后的潜在生物标志物。
Front Oncol. 2025 Jun 4;15:1547067. doi: 10.3389/fonc.2025.1547067. eCollection 2025.
9
Early Immunological and Inflammation Proteomic Changes in Elderly COVID-19 Patients Predict Severe Disease Progression.老年新冠患者早期免疫和炎症蛋白质组学变化可预测疾病严重进展
Biomedicines. 2025 May 10;13(5):1162. doi: 10.3390/biomedicines13051162.
10
Role of the tumor microenvironment in cancer therapy: unveiling new targets to overcome drug resistance.肿瘤微环境在癌症治疗中的作用:揭示克服耐药性的新靶点。
Med Oncol. 2025 May 7;42(6):202. doi: 10.1007/s12032-025-02754-w.

本文引用的文献

1
Increased levels of granulocytic myeloid-derived suppressor cells in peripheral blood and tumour tissue of pancreatic cancer patients.胰腺癌患者外周血和肿瘤组织中粒细胞性髓源抑制细胞水平升高。
J Immunol Res. 2014;2014:879897. doi: 10.1155/2014/879897. Epub 2014 Jan 29.
2
Tumor-induced STAT3 activation in monocytic myeloid-derived suppressor cells enhances stemness and mesenchymal properties in human pancreatic cancer.肿瘤诱导的单核细胞来源的髓样抑制细胞中的 STAT3 激活增强了人胰腺癌细胞的干性和间充质特性。
Cancer Immunol Immunother. 2014 May;63(5):513-28. doi: 10.1007/s00262-014-1527-x. Epub 2014 Mar 21.
3
Transmembrane TNF-α promotes suppressive activities of myeloid-derived suppressor cells via TNFR2.跨膜 TNF-α 通过 TNFR2 促进髓源性抑制细胞的抑制活性。
J Immunol. 2014 Feb 1;192(3):1320-31. doi: 10.4049/jimmunol.1203195. Epub 2013 Dec 30.
4
Circulating immune cell and microRNA in patients with uveal melanoma developing metastatic disease.葡萄膜黑色素瘤发生转移患者的循环免疫细胞和 microRNA。
Mol Immunol. 2014 Apr;58(2):182-6. doi: 10.1016/j.molimm.2013.11.018. Epub 2013 Dec 25.
5
Frequencies of circulating MDSC correlate with clinical outcome of melanoma patients treated with ipilimumab.循环 MDSC 的频率与接受伊匹单抗治疗的黑色素瘤患者的临床结果相关。
Cancer Immunol Immunother. 2014 Mar;63(3):247-57. doi: 10.1007/s00262-013-1508-5. Epub 2013 Dec 20.
6
Myeloid-derived suppressor cells predict survival of patients with advanced melanoma: comparison with regulatory T cells and NY-ESO-1- or melan-A-specific T cells.髓源性抑制细胞预测晚期黑色素瘤患者的生存:与调节性 T 细胞和 NY-ESO-1 或黑色素瘤-A 特异性 T 细胞的比较。
Clin Cancer Res. 2014 Mar 15;20(6):1601-9. doi: 10.1158/1078-0432.CCR-13-2508. Epub 2013 Dec 9.
7
CXCR2-expressing myeloid-derived suppressor cells are essential to promote colitis-associated tumorigenesis.表达 CXCR2 的髓源性抑制细胞对于促进结肠炎相关肿瘤发生是必不可少的。
Cancer Cell. 2013 Nov 11;24(5):631-44. doi: 10.1016/j.ccr.2013.10.009.
8
Myeloid-derived suppressor cell development is regulated by a STAT/IRF-8 axis.髓源性抑制细胞的发育受 STAT/IRF-8 轴的调节。
J Clin Invest. 2013 Oct;123(10):4464-78. doi: 10.1172/JCI68189. Epub 2013 Sep 16.
9
History of myeloid-derived suppressor cells.髓系来源的抑制性细胞的历史。
Nat Rev Cancer. 2013 Oct;13(10):739-52. doi: 10.1038/nrc3581.
10
A mutual activation loop between breast cancer cells and myeloid-derived suppressor cells facilitates spontaneous metastasis through IL-6 trans-signaling in a murine model.在小鼠模型中,乳腺癌细胞与髓源性抑制细胞之间的相互激活环通过IL-6转信号促进自发转移。
Breast Cancer Res. 2013;15(5):R79. doi: 10.1186/bcr3473.

髓源性抑制细胞对肿瘤转移的调控

Regulation of tumor metastasis by myeloid-derived suppressor cells.

作者信息

Condamine Thomas, Ramachandran Indu, Youn Je-In, Gabrilovich Dmitry I

机构信息

The Wistar Institute, Philadelphia, Pennsylvania 19104; email:

出版信息

Annu Rev Med. 2015;66:97-110. doi: 10.1146/annurev-med-051013-052304. Epub 2014 Oct 9.

DOI:10.1146/annurev-med-051013-052304
PMID:25341012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4324727/
Abstract

Accumulation of pathologically activated immature myeloid cells with potent immune-suppressive activity is one of the major immunological hallmarks of cancer. In recent years, it became clear that in addition to their immune-suppressive activity, myeloid-derived suppressor cells (MDSCs) influence tumor progression in a variety of ways. They are directly implicated in the promotion of tumor metastases by participating in the formation of premetastatic niches, promoting angiogenesis and tumor cell invasion. In this review, we discuss recent data describing various roles of MDSCs in the formation of tumor metastases.

摘要

具有强大免疫抑制活性的病理活化未成熟髓样细胞的积累是癌症的主要免疫特征之一。近年来,越来越清楚的是,髓源性抑制细胞(MDSC)除了具有免疫抑制活性外,还以多种方式影响肿瘤进展。它们通过参与前转移生态位的形成、促进血管生成和肿瘤细胞侵袭,直接参与促进肿瘤转移。在这篇综述中,我们讨论了描述MDSC在肿瘤转移形成中各种作用的最新数据。