• 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

髓系来源抑制细胞在前列腺癌中的作用:现状与展望。

Myeloid-Derived Suppressor Cells in Prostate Cancer: Present Knowledge and Future Perspectives.

机构信息

Department of Medical Oncology, University General Hospital of Larissa, 41221 Larissa, Thessaly, Greece.

Laboratory of Oncology, Faculty of Medicine, School of Health Sciences, University of Thessaly, 41500 Larissa, Thessaly, Greece.

出版信息

Cells. 2021 Dec 22;11(1):20. doi: 10.3390/cells11010020.

DOI:10.3390/cells11010020
PMID:35011582
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8750906/
Abstract

Several lines of research are being investigated to better understand mechanisms implicated in response or resistance to immune checkpoint blockade in prostate cancer (PCa). Myeloid-derived suppressor cells (MDSCs) have emerged as a major mediator of immunosuppression in the tumor microenvironment that promotes progression of various tumor types. The main mechanisms underlying MDSC-induced immunosuppression are currently being explored and strategies to enhance anti-tumor immune response via MDSC targeting are being tested. However, the role of MDSCs in PCa remains elusive. In this review, we aim to summarize and present the state-of-the-art knowledge on current methodologies to phenotypically and metabolically characterize MDSCs in PCa. We describe how these characteristics may be linked with MDSC function and may influence the clinical outcomes of patients with PCa. Finally, we briefly discuss emerging strategies being employed to therapeutically target MDSCs and potentiate the long-overdue improvement in the efficacy of immunotherapy in patients with PCa.

摘要

目前,有几条研究路线正在探索,以更好地了解前列腺癌(PCa)中免疫检查点阻断反应或耐药的相关机制。髓源抑制细胞(MDSCs)已成为肿瘤微环境中主要的免疫抑制介质,促进了多种肿瘤类型的进展。目前正在探索 MDSC 诱导的免疫抑制的主要机制,并正在测试通过 MDSC 靶向增强抗肿瘤免疫反应的策略。然而,MDSCs 在 PCa 中的作用仍不清楚。在这篇综述中,我们旨在总结和介绍目前用于表型和代谢特征分析 PCa 中 MDSCs 的最新方法学知识。我们描述了这些特征如何与 MDSC 功能相关,并可能影响 PCa 患者的临床结局。最后,我们简要讨论了新兴的治疗性靶向 MDSC 的策略,并增强免疫疗法在 PCa 患者中的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebad/8750906/00fbfd1e244d/cells-11-00020-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebad/8750906/00fbfd1e244d/cells-11-00020-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebad/8750906/00fbfd1e244d/cells-11-00020-g001.jpg

相似文献

1
Myeloid-Derived Suppressor Cells in Prostate Cancer: Present Knowledge and Future Perspectives.髓系来源抑制细胞在前列腺癌中的作用:现状与展望。
Cells. 2021 Dec 22;11(1):20. doi: 10.3390/cells11010020.
2
Targeting myeloid-derived suppressor cells in tumor immunotherapy: Current, future and beyond.靶向肿瘤免疫治疗中的髓源抑制细胞:当前、未来及以后。
Front Immunol. 2023 Mar 17;14:1157537. doi: 10.3389/fimmu.2023.1157537. eCollection 2023.
3
The New Era of Cancer Immunotherapy: Targeting Myeloid-Derived Suppressor Cells to Overcome Immune Evasion.癌症免疫治疗的新时代:靶向髓系来源抑制细胞以克服免疫逃逸。
Front Immunol. 2020 Jul 30;11:1680. doi: 10.3389/fimmu.2020.01680. eCollection 2020.
4
Targeting the crosstalk between cytokine-induced killer cells and myeloid-derived suppressor cells in hepatocellular carcinoma.靶向细胞因子诱导的杀伤细胞与髓系来源抑制细胞在肝癌中的相互作用。
J Hepatol. 2019 Mar;70(3):449-457. doi: 10.1016/j.jhep.2018.10.040. Epub 2018 Nov 9.
5
Immunotherapy of targeting MDSCs in tumor microenvironment.在肿瘤微环境中针对髓系来源抑制细胞的免疫治疗。
Front Immunol. 2022 Sep 5;13:990463. doi: 10.3389/fimmu.2022.990463. eCollection 2022.
6
Myeloid-derived suppressor cells: an emerging target for anticancer immunotherapy.髓系来源的抑制细胞:抗肿瘤免疫治疗的一个新靶点。
Mol Cancer. 2022 Sep 26;21(1):184. doi: 10.1186/s12943-022-01657-y.
7
A new histone deacetylase inhibitor remodels the tumor microenvironment by deletion of polymorphonuclear myeloid-derived suppressor cells and sensitizes prostate cancer to immunotherapy.一种新型组蛋白去乙酰化酶抑制剂通过消除多形核髓系来源的抑制性细胞重塑肿瘤微环境,并使前列腺癌对免疫治疗敏感。
BMC Med. 2023 Oct 25;21(1):402. doi: 10.1186/s12916-023-03094-0.
8
TLR9 expression and secretion of LIF by prostate cancer cells stimulates accumulation and activity of polymorphonuclear MDSCs.前列腺癌细胞中TLR9的表达及白血病抑制因子的分泌会刺激多形核髓源性抑制细胞的积聚及活性。
J Leukoc Biol. 2017 Aug;102(2):423-436. doi: 10.1189/jlb.3MA1016-451RR. Epub 2017 May 22.
9
Myeloid-Derived Suppressor Cells in the Tumor Microenvironment.肿瘤微环境中的髓源性抑制细胞。
Adv Exp Med Biol. 2020;1224:117-140. doi: 10.1007/978-3-030-35723-8_8.
10
CD200 promotes immunosuppression in the pancreatic tumor microenvironment.CD200 促进胰腺肿瘤微环境中的免疫抑制。
J Immunother Cancer. 2020 Jun;8(1). doi: 10.1136/jitc-2019-000189. Epub 2020 Jun 23.

引用本文的文献

1
New Insights into Potential Therapeutic Targets for Neuroendocrine Prostate Cancer: From Bench to Clinic.神经内分泌前列腺癌潜在治疗靶点的新见解:从实验室到临床
Research (Wash D C). 2025 Jul 31;8:0791. doi: 10.34133/research.0791. eCollection 2025.
2
ARTREM2 macrophage induced pathogenic immunosuppression promotes prostate cancer progression.ARTREM2巨噬细胞诱导的致病性免疫抑制促进前列腺癌进展。
Nat Commun. 2025 Jul 29;16(1):6964. doi: 10.1038/s41467-025-62381-x.
3
Role of Tumor Microenvironment in Prostate Cancer Immunometabolism.

本文引用的文献

1
Castration-mediated IL-8 promotes myeloid infiltration and prostate cancer progression.去势介导的白细胞介素-8促进髓样细胞浸润和前列腺癌进展。
Nat Cancer. 2021 Aug;2(8):803-818. doi: 10.1038/s43018-021-00227-3. Epub 2021 Jul 19.
2
A phase III, randomized, open-label study (CONTACT-02) of cabozantinib plus atezolizumab versus second novel hormone therapy in patients with metastatic castration-resistant prostate cancer.一项卡博替尼联合阿替利珠单抗与二线新型激素治疗转移性去势抵抗性前列腺癌患者的 III 期、随机、开放标签研究(CONTACT-02)。
Future Oncol. 2022 Mar;18(10):1185-1198. doi: 10.2217/fon-2021-1096. Epub 2022 Jan 17.
3
肿瘤微环境在前列腺癌免疫代谢中的作用
Biomolecules. 2025 Jun 6;15(6):826. doi: 10.3390/biom15060826.
4
PI3Kδ as a Novel Therapeutic Target for Aggressive Prostate Cancer.PI3Kδ作为侵袭性前列腺癌的新型治疗靶点。
Cancers (Basel). 2025 May 9;17(10):1610. doi: 10.3390/cancers17101610.
5
Immunotherapy in Prostate Cancer: From a "Cold" Tumor to a "Hot" Prospect.前列腺癌的免疫疗法:从“冷”肿瘤到“热”前景
Cancers (Basel). 2025 Mar 21;17(7):1064. doi: 10.3390/cancers17071064.
6
Targeting the tumour cell surface in advanced prostate cancer.靶向晚期前列腺癌的肿瘤细胞表面
Nat Rev Urol. 2025 Apr 1. doi: 10.1038/s41585-025-01014-w.
7
The role of neutrophils and their immunosuppressive effects on prostate cancer.中性粒细胞的作用及其对前列腺癌的免疫抑制作用。
Histol Histopathol. 2025 Sep;40(9):1347-1353. doi: 10.14670/HH-18-890. Epub 2025 Feb 20.
8
Evolution of myeloid-mediated immunotherapy resistance in prostate cancer.前列腺癌中髓系介导的免疫治疗耐药性的演变
Nature. 2025 Jan;637(8048):1207-1217. doi: 10.1038/s41586-024-08290-3. Epub 2024 Dec 4.
9
Prognostic Value of PlGF Upregulation in Prostate Cancer.胎盘生长因子上调在前列腺癌中的预后价值
Biomedicines. 2024 Sep 26;12(10):2194. doi: 10.3390/biomedicines12102194.
10
Iron-loaded cancer-associated fibroblasts induce immunosuppression in prostate cancer.铁负荷的肿瘤相关成纤维细胞诱导前列腺癌中的免疫抑制。
Nat Commun. 2024 Oct 20;15(1):9050. doi: 10.1038/s41467-024-53233-1.
β2-adrenergic receptor signaling regulates metabolic pathways critical to myeloid-derived suppressor cell function within the TME.
β2-肾上腺素能受体信号调节代谢途径,这些途径对肿瘤微环境中髓源性抑制细胞的功能至关重要。
Cell Rep. 2021 Oct 26;37(4):109883. doi: 10.1016/j.celrep.2021.109883.
4
Phase I Study of Entinostat in Combination with Enzalutamide for Treatment of Patients with Metastatic Castration-Resistant Prostate Cancer.依沙替康联合恩杂鲁胺治疗转移性去势抵抗性前列腺癌的 I 期研究。
Oncologist. 2021 Dec;26(12):e2136-e2142. doi: 10.1002/onco.13957. Epub 2021 Sep 14.
5
Tumor-related stress regulates functional plasticity of MDSCs.肿瘤相关应激调节髓系来源抑制细胞的功能可塑性。
Cell Immunol. 2021 May;363:104312. doi: 10.1016/j.cellimm.2021.104312. Epub 2021 Feb 12.
6
Prostaglandin E2 and Cancer: Insight into Tumor Progression and Immunity.前列腺素E2与癌症:对肿瘤进展和免疫的洞察
Biology (Basel). 2020 Dec 1;9(12):434. doi: 10.3390/biology9120434.
7
CXCR4 inhibition in human pancreatic and colorectal cancers induces an integrated immune response.CXCR4 抑制在人类胰腺和结直肠癌细胞中诱导整合免疫反应。
Proc Natl Acad Sci U S A. 2020 Nov 17;117(46):28960-28970. doi: 10.1073/pnas.2013644117. Epub 2020 Oct 30.
8
CXCR4 Inhibition Counteracts Immunosuppressive Properties of Metastatic NSCLC Stem Cells.CXCR4 抑制作用可逆转转移性 NSCLC 干细胞的免疫抑制特性。
Front Immunol. 2020 Oct 2;11:02168. doi: 10.3389/fimmu.2020.02168. eCollection 2020.
9
Enzalutamide, an Androgen Receptor Antagonist, Enhances Myeloid Cell-Mediated Immune Suppression and Tumor Progression.恩杂鲁胺,一种雄激素受体拮抗剂,增强髓系细胞介导的免疫抑制和肿瘤进展。
Cancer Immunol Res. 2020 Sep;8(9):1215-1227. doi: 10.1158/2326-6066.CIR-19-0371. Epub 2020 Jul 13.
10
Myeloid Cell-Derived Arginase in Cancer Immune Response.髓系细胞衍生的精氨酸酶在癌症免疫反应中的作用
Front Immunol. 2020 May 15;11:938. doi: 10.3389/fimmu.2020.00938. eCollection 2020.