• 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

微环境代谢调控抗肿瘤免疫。

Microenvironmental Metabolism Regulates Antitumor Immunity.

机构信息

Program in Cancer Biology, Vanderbilt University, Nashville, Tennessee.

Division of Rheumatology and Immunology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

出版信息

Cancer Res. 2019 Aug 15;79(16):4003-4008. doi: 10.1158/0008-5472.CAN-19-0617. Epub 2019 Jul 30.

DOI:10.1158/0008-5472.CAN-19-0617
PMID:31362930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6697577/
Abstract

Metabolic reprogramming of cancer cells and the tumor microenvironment are emerging as key factors governing tumor growth, metastasis, and response to therapies including immune checkpoint inhibitors. It has been recognized that rapidly proliferating cancer cells, tumor-infiltrating lymphocytes, and vascular endothelial cells compete for oxygen and nutrients. Tumor cells and other cell types in the microenvironment not only compete for nutrients, but they also simultaneously produce immunosuppressive metabolites, leading to immune escape. In addition, commensal microbial metabolites can influence regulatory T cells and inflammation in the intestine, thus playing an essential role in cancer prevention or cancer promotion. In this review, we summarize recent advances on metabolic interactions among various cell types in the tumor microenvironment, with a focus on how these interactions affect tumor immunity. We also discuss the potential role of blood vessel metabolism in regulating immune cell trafficking and activation.

摘要

肿瘤细胞和肿瘤微环境的代谢重编程正在成为控制肿瘤生长、转移以及对包括免疫检查点抑制剂在内的治疗方法的反应的关键因素。人们已经认识到,快速增殖的癌细胞、肿瘤浸润淋巴细胞和血管内皮细胞争夺氧气和营养物质。肿瘤细胞和微环境中的其他细胞类型不仅争夺营养物质,而且还同时产生免疫抑制代谢物,导致免疫逃逸。此外,共生微生物代谢物可以影响肠道中的调节性 T 细胞和炎症,从而在癌症预防或促进中发挥重要作用。在这篇综述中,我们总结了肿瘤微环境中各种细胞类型之间代谢相互作用的最新进展,重点讨论了这些相互作用如何影响肿瘤免疫。我们还讨论了血管代谢在调节免疫细胞迁移和激活中的潜在作用。

相似文献

1
Microenvironmental Metabolism Regulates Antitumor Immunity.微环境代谢调控抗肿瘤免疫。
Cancer Res. 2019 Aug 15;79(16):4003-4008. doi: 10.1158/0008-5472.CAN-19-0617. Epub 2019 Jul 30.
2
MondoA-Thioredoxin-Interacting Protein Axis Maintains Regulatory T-Cell Identity and Function in Colorectal Cancer Microenvironment.MondoA-硫氧还蛋白相互作用蛋白轴在结直肠癌微环境中维持调节性 T 细胞的特性和功能。
Gastroenterology. 2021 Aug;161(2):575-591.e16. doi: 10.1053/j.gastro.2021.04.041. Epub 2021 Apr 24.
3
Association of Fusobacterium nucleatum with immunity and molecular alterations in colorectal cancer.具核梭杆菌与结直肠癌免疫及分子改变的关联
World J Gastroenterol. 2016 Jan 14;22(2):557-66. doi: 10.3748/wjg.v22.i2.557.
4
Metabolic Reprogramming of Colorectal Cancer Cells and the Microenvironment: Implication for Therapy.结直肠癌细胞及其微环境的代谢重编程:治疗意义。
Int J Mol Sci. 2021 Jun 10;22(12):6262. doi: 10.3390/ijms22126262.
5
Distribution of Regulatory T-Cells and Other Phenotypes of T-Cells in Tumors and Regional Lymph Nodes of Colorectal Cancer Patients.结直肠癌患者肿瘤及区域淋巴结中调节性 T 细胞及其他 T 细胞表型的分布。
In Vivo. 2020 Mar-Apr;34(2):849-856. doi: 10.21873/invivo.11848.
6
Metabolic reprogramming in the tumour microenvironment: a hallmark shared by cancer cells and T lymphocytes.肿瘤微环境中的代谢重编程:癌细胞与T淋巴细胞的共同特征。
Immunology. 2017 Oct;152(2):175-184. doi: 10.1111/imm.12777. Epub 2017 Jul 10.
7
T cell subsets and colorectal cancer: discerning the good from the bad.T 细胞亚群与结直肠癌:明辨良莠。
Cell Immunol. 2012 Sep;279(1):21-4. doi: 10.1016/j.cellimm.2012.08.004. Epub 2012 Sep 14.
8
Tumor-Infiltrating Lymphocytes in Colorectal Cancer: The Fundamental Indication and Application on Immunotherapy.结直肠癌中的肿瘤浸润淋巴细胞:免疫治疗的基本指征和应用。
Front Immunol. 2022 Jan 14;12:808964. doi: 10.3389/fimmu.2021.808964. eCollection 2021.
9
A comparison of the local immune status between the primary and metastatic tumor in colorectal cancer: a retrospective study.结直肠癌原发灶与转移灶局部免疫状态的比较:一项回顾性研究。
BMC Cancer. 2018 Apr 3;18(1):371. doi: 10.1186/s12885-018-4276-y.
10
Analysis of Spatial Organization of Suppressive Myeloid Cells and Effector T Cells in Colorectal Cancer-A Potential Tool for Discovering Prognostic Biomarkers in Clinical Research.分析结直肠癌中抑制性髓系细胞和效应 T 细胞的空间组织——在临床研究中发现预后生物标志物的潜在工具。
Front Immunol. 2020 Oct 29;11:550250. doi: 10.3389/fimmu.2020.550250. eCollection 2020.

引用本文的文献

1
A novel lactylation-related signature for predicting esophageal cancer prognosis and immune infiltration.一种用于预测食管癌预后和免疫浸润的新型乳酸化相关特征。
J Gastrointest Oncol. 2025 Aug 30;16(4):1711-1735. doi: 10.21037/jgo-2024-1006. Epub 2025 Aug 26.
2
Trends and hotspots in research related to tumor immune escape: bibliometric analysis and future perspectives.肿瘤免疫逃逸相关研究的趋势与热点:文献计量分析及未来展望
Front Immunol. 2025 Aug 28;16:1604216. doi: 10.3389/fimmu.2025.1604216. eCollection 2025.
3
Delivery-Graded Programmable Micelles Achieve Enhanced Tumor Starvation through Combined Glutamine Deprivation and Angiogenesis Inhibition.递送分级可编程胶束通过联合谷氨酰胺剥夺和血管生成抑制实现增强的肿瘤饥饿疗法。
Research (Wash D C). 2025 Sep 5;5:0858. doi: 10.34133/research.0858. eCollection 2025.
4
Targeting myeloid cells to improve cancer immune therapy.靶向髓样细胞以改善癌症免疫治疗。
Front Immunol. 2025 Jul 31;16:1623436. doi: 10.3389/fimmu.2025.1623436. eCollection 2025.
5
Histone lactylation: a new target for overcoming immune evasion and therapy resistance.组蛋白乳酰化:克服免疫逃逸和治疗抗性的新靶点。
Med Oncol. 2025 Aug 2;42(9):399. doi: 10.1007/s12032-025-02940-w.
6
Lactylation and viral infections: A novel link between metabolic reprogramming and immune regulation.乳酰化与病毒感染:代谢重编程与免疫调节之间的新联系。
PLoS Pathog. 2025 Jul 28;21(7):e1013366. doi: 10.1371/journal.ppat.1013366. eCollection 2025 Jul.
7
Fungi and cancer: unveiling the complex role of fungal infections in tumor biology and therapeutic resistance.真菌与癌症:揭示真菌感染在肿瘤生物学和治疗耐药性中的复杂作用
Front Cell Infect Microbiol. 2025 Jun 10;15:1596688. doi: 10.3389/fcimb.2025.1596688. eCollection 2025.
8
Natural Killer Cell Immune Checkpoints and Their Therapeutic Targeting in Cancer Treatment.自然杀伤细胞免疫检查点及其在癌症治疗中的靶向治疗
Research (Wash D C). 2025 Jun 3;8:0723. doi: 10.34133/research.0723. eCollection 2025.
9
Immunomodulatory behavior of CircRNAs in tumor microenvironment.环状RNA在肿瘤微环境中的免疫调节行为
Oncol Res. 2025 Apr 18;33(5):1105-1119. doi: 10.32604/or.2024.054623. eCollection 2025.
10
Heterogeneity of Neutrophils and Immunological Function in Neonatal Sepsis: Analysis of Molecular Subtypes Based on Hypoxia-Glycolysis-Lactylation.新生儿脓毒症中中性粒细胞的异质性及免疫功能:基于缺氧-糖酵解-乳酸化的分子亚型分析
Mediators Inflamm. 2025 Mar 26;2025:5790261. doi: 10.1155/mi/5790261. eCollection 2025.

本文引用的文献

1
Normalizing Function of Tumor Vessels: Progress, Opportunities, and Challenges.肿瘤血管正常化功能:进展、机遇与挑战。
Annu Rev Physiol. 2019 Feb 10;81:505-534. doi: 10.1146/annurev-physiol-020518-114700.
2
A defined commensal consortium elicits CD8 T cells and anti-cancer immunity.特定共生菌群可诱导 CD8+T 细胞及抗肿瘤免疫。
Nature. 2019 Jan;565(7741):600-605. doi: 10.1038/s41586-019-0878-z. Epub 2019 Jan 23.
3
Fecal microbiota transplantation for refractory immune checkpoint inhibitor-associated colitis.粪便微生物群移植治疗难治性免疫检查点抑制剂相关性结肠炎。
Nat Med. 2018 Dec;24(12):1804-1808. doi: 10.1038/s41591-018-0238-9. Epub 2018 Nov 12.
4
Distinct Regulation of Th17 and Th1 Cell Differentiation by Glutaminase-Dependent Metabolism.谷氨酰胺酶依赖性代谢对 Th17 和 Th1 细胞分化的不同调节。
Cell. 2018 Dec 13;175(7):1780-1795.e19. doi: 10.1016/j.cell.2018.10.001. Epub 2018 Nov 1.
5
TLR8-Mediated Metabolic Control of Human Treg Function: A Mechanistic Target for Cancer Immunotherapy.TLR8 介导的人类 Treg 功能代谢控制:癌症免疫治疗的机制靶点。
Cell Metab. 2019 Jan 8;29(1):103-123.e5. doi: 10.1016/j.cmet.2018.09.020. Epub 2018 Oct 18.
6
IRE1α-XBP1 controls T cell function in ovarian cancer by regulating mitochondrial activity.IRE1α-XBP1 通过调节线粒体活性控制卵巢癌中的 T 细胞功能。
Nature. 2018 Oct;562(7727):423-428. doi: 10.1038/s41586-018-0597-x. Epub 2018 Oct 10.
7
Human Organ-Specific Endothelial Cell Heterogeneity.人类器官特异性内皮细胞异质性
iScience. 2018 Jun 29;4:20-35. doi: 10.1016/j.isci.2018.05.003. Epub 2018 May 9.
8
Aerobic Glycolysis Controls Myeloid-Derived Suppressor Cells and Tumor Immunity via a Specific CEBPB Isoform in Triple-Negative Breast Cancer.有氧糖酵解通过三阴性乳腺癌中特定的 CEBPB 异构体控制髓源性抑制细胞和肿瘤免疫。
Cell Metab. 2018 Jul 3;28(1):87-103.e6. doi: 10.1016/j.cmet.2018.04.022. Epub 2018 May 24.
9
Enhancing cancer immunotherapy using antiangiogenics: opportunities and challenges.利用抗血管生成药物增强癌症免疫治疗:机遇与挑战。
Nat Rev Clin Oncol. 2018 May;15(5):325-340. doi: 10.1038/nrclinonc.2018.29. Epub 2018 Mar 6.
10
Pharmacological blockade of ASCT2-dependent glutamine transport leads to antitumor efficacy in preclinical models.药理学阻断 ASCT2 依赖性谷氨酰胺转运可在临床前模型中发挥抗肿瘤疗效。
Nat Med. 2018 Feb;24(2):194-202. doi: 10.1038/nm.4464. Epub 2018 Jan 15.