• 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

癌症与免疫疗法中的血小板:功能动态与治疗机遇

Platelets in cancer and immunotherapy: functional dynamics and therapeutic opportunities.

作者信息

Cai Changjing, Liu Yiting, Lu Ruohuang, Fan Xudong, Zeng Shan, Gan Pingping

机构信息

Department of Oncology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.

出版信息

Exp Hematol Oncol. 2025 Jun 13;14(1):83. doi: 10.1186/s40164-025-00676-x.

DOI:10.1186/s40164-025-00676-x
PMID:40514754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12166581/
Abstract

Platelets play a critical role in tumor immunity, particularly in promoting cancer progression. Numerous studies suggest that platelets could serve as a novel target for cancer immunotherapy, however, no comprehensive reviews have yet summarized and discussed this potential. Our review provides an in-depth discussion of the roles and mechanisms of platelets within both the immunosuppressive tumor microenvironment and the anti-tumor immune microenvironment. Additionally, we summarize the key therapeutic targets and approaches for clinical translation. This work offers essential insights for reprogramming platelets to shift their function from tumor promotion to tumor suppression, providing a foundation for the development of novel immunotherapeutic strategies and related research.

摘要

血小板在肿瘤免疫中发挥着关键作用,尤其是在促进癌症进展方面。众多研究表明,血小板可作为癌症免疫治疗的新靶点,然而,尚无全面综述对这一潜力进行总结和讨论。我们的综述深入探讨了血小板在免疫抑制性肿瘤微环境和抗肿瘤免疫微环境中的作用及机制。此外,我们总结了临床转化的关键治疗靶点和方法。这项工作为重新编程血小板以将其功能从促进肿瘤转变为抑制肿瘤提供了重要见解,为新型免疫治疗策略及相关研究的发展奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/afb73938c019/40164_2025_676_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/39a1aec71ade/40164_2025_676_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/a30836f134bf/40164_2025_676_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/afb73938c019/40164_2025_676_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/39a1aec71ade/40164_2025_676_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/a30836f134bf/40164_2025_676_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b02d/12166581/afb73938c019/40164_2025_676_Fig3_HTML.jpg

相似文献

1
Platelets in cancer and immunotherapy: functional dynamics and therapeutic opportunities.癌症与免疫疗法中的血小板:功能动态与治疗机遇
Exp Hematol Oncol. 2025 Jun 13;14(1):83. doi: 10.1186/s40164-025-00676-x.
2
The roles of epigallocatechin gallate in the tumor microenvironment, metabolic reprogramming, and immunotherapy.没食子儿茶素没食子酸酯在肿瘤微环境、代谢重编程和免疫治疗中的作用。
Front Immunol. 2024 Jan 29;15:1331641. doi: 10.3389/fimmu.2024.1331641. eCollection 2024.
3
Revealing profile of cancer-educated platelets and their factors to foster immunotherapy development.揭示受过癌症教育的血小板及其促进免疫治疗发展的因素。
Transl Oncol. 2024 Feb;40:101871. doi: 10.1016/j.tranon.2023.101871. Epub 2023 Dec 21.
4
Targeting platelet-tumor cell interactions: a novel approach to cancer therapy.靶向血小板-肿瘤细胞相互作用:一种癌症治疗的新方法。
Med Oncol. 2025 Jun 2;42(7):232. doi: 10.1007/s12032-025-02787-1.
5
Platelet-Mediated Protection of Cancer Cells From Immune Surveillance - Possible Implications for Cancer Immunotherapy.血小板介导的癌细胞免疫逃避及其对癌症免疫治疗的启示
Front Immunol. 2021 Mar 10;12:640578. doi: 10.3389/fimmu.2021.640578. eCollection 2021.
6
Interactions between platelets and the cancer immune microenvironment.血小板与肿瘤免疫微环境的相互作用。
Crit Rev Oncol Hematol. 2024 Jul;199:104380. doi: 10.1016/j.critrevonc.2024.104380. Epub 2024 May 7.
7
Epigenetic modulation of antitumor immunity for improved cancer immunotherapy.表观遗传调控抗肿瘤免疫以改善癌症免疫治疗。
Mol Cancer. 2021 Dec 20;20(1):171. doi: 10.1186/s12943-021-01464-x.
8
Reprogramming the immunosuppressive tumor microenvironment through nanomedicine: an immunometabolism perspective.通过纳米医学重编程免疫抑制性肿瘤微环境:免疫代谢观点。
EBioMedicine. 2024 Sep;107:105301. doi: 10.1016/j.ebiom.2024.105301. Epub 2024 Aug 22.
9
Metabolic reprogramming, autophagy, and ferroptosis: Novel arsenals to overcome immunotherapy resistance in gastrointestinal cancer.代谢重编程、自噬和铁死亡:克服胃肠道癌症免疫治疗耐药性的新武器。
Cancer Med. 2023 Nov;12(21):20573-20589. doi: 10.1002/cam4.6623. Epub 2023 Oct 20.
10
Choline metabolism reprogramming mediates an immunosuppressive microenvironment in non-small cell lung cancer (NSCLC) by promoting tumor-associated macrophage functional polarization and endothelial cell proliferation.胆碱代谢重编程通过促进肿瘤相关巨噬细胞功能极化和内皮细胞增殖来介导非小细胞肺癌(NSCLC)中的免疫抑制微环境。
J Transl Med. 2024 May 10;22(1):442. doi: 10.1186/s12967-024-05242-3.

本文引用的文献

1
Aspirin prevents metastasis by limiting platelet TXA suppression of T cell immunity.阿司匹林通过限制血小板血栓素对T细胞免疫的抑制作用来预防转移。
Nature. 2025 Apr;640(8060):1052-1061. doi: 10.1038/s41586-025-08626-7. Epub 2025 Mar 5.
2
Immune microenvironment of Epstein-Barr virus (EBV)-negative compared to EBV-associated gastric cancers: implications for immunotherapy.与 EBV 相关胃癌相比,EBV 阴性胃癌的免疫微环境:免疫治疗的意义。
J Immunother Cancer. 2024 Nov 20;12(11):e010201. doi: 10.1136/jitc-2024-010201.
3
Phase II trial of pembrolizumab, ipilimumab, and aspirin in melanoma: clinical outcomes and translational predictors of response.
帕博利珠单抗、伊匹木单抗和阿司匹林治疗黑色素瘤的II期试验:临床结果及反应的转化预测指标
BJC Rep. 2024 Jun 24;2(1):46. doi: 10.1038/s44276-024-00057-7.
4
Prostaglandin E-EP2/EP4 signaling induces immunosuppression in human cancer by impairing bioenergetics and ribosome biogenesis in immune cells.前列腺素 E-EP2/EP4 信号通过损害免疫细胞的生物能量和核糖体生物发生来诱导人类癌症中的免疫抑制。
Nat Commun. 2024 Nov 1;15(1):9464. doi: 10.1038/s41467-024-53706-3.
5
Aspirin Hypersensitivity in Patients With Atherosclerotic Cardiovascular Disease.阿司匹林过敏患者的动脉粥样硬化性心血管疾病。
J Am Coll Cardiol. 2024 Oct 29;84(18):1748-1766. doi: 10.1016/j.jacc.2024.05.084.
6
AMDHD1 acts as a tumor suppressor and contributes to activation of TGF-β signaling pathway in cholangiocarcinoma.AMDHD1作为一种肿瘤抑制因子,在胆管癌中有助于激活转化生长因子-β信号通路。
Cell Death Differ. 2025 Jan;32(1):162-176. doi: 10.1038/s41418-024-01361-y. Epub 2024 Aug 14.
7
Blocking CX3CR1+ Tumor-Associated Macrophages Enhances the Efficacy of Anti-PD1 Therapy in Hepatocellular Carcinoma.阻断 CX3CR1+肿瘤相关巨噬细胞增强抗 PD-1 疗法在肝细胞癌中的疗效。
Cancer Immunol Res. 2024 Nov 4;12(11):1603-1620. doi: 10.1158/2326-6066.CIR-23-0627.
8
Platelet TGF-β triggers immunosuppression in ITP.血小板转化生长因子-β引发免疫性血小板减少症中的免疫抑制。
Blood. 2024 Jul 4;144(1):7-8. doi: 10.1182/blood.2024024825.
9
PD-1 blockade plus COX inhibitors in dMMR metastatic colorectal cancer: Clinical, genomic, and immunologic analyses from the PCOX trial.PD-1 阻断联合 COX 抑制剂治疗错配修复缺陷转移性结直肠癌:来自 PCOX 试验的临床、基因组和免疫分析。
Med. 2024 Aug 9;5(8):998-1015.e6. doi: 10.1016/j.medj.2024.05.002. Epub 2024 May 24.
10
Platelet-mediated circulating tumor cell evasion from natural killer cell killing through immune checkpoint CD155-TIGIT.血小板介导循环肿瘤细胞通过免疫检查点CD155-TIGIT逃避自然杀伤细胞的杀伤。
Hepatology. 2025 Mar 1;81(3):791-807. doi: 10.1097/HEP.0000000000000934. Epub 2024 May 23.