• 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

结直肠癌中转移相关巨噬细胞的特征分析用于预后预测和免疫代谢重塑。

Characterization of metastasis-specific macrophages in colorectal cancer for prognosis prediction and immunometabolic remodeling.

机构信息

Department of colorectal surgery, Tianjin Union Medical Center, Tianjin, 300122, China.

Tianjin Institute of Coloproctology, Tianjin, 300122, China.

出版信息

Sci Rep. 2024 Nov 1;14(1):26361. doi: 10.1038/s41598-024-77248-2.

DOI:10.1038/s41598-024-77248-2
PMID:39487182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11530676/
Abstract

This study develops a prognostic model to predict metastasis and prognosis in colorectal cancer liver metastases by identifying distinct macrophage subsets. Using scRNA-seq data from primary colorectal cancer and liver metastases, we dissected the cellular landscape to find unique macrophage subpopulations, particularly EEF1G + macrophages, which were prevalent in liver metastases. The study leveraged data from GSE231559, TCGA, and GEO databases to construct an 8-gene risk model named EMGS, based on the EEF1G + macrophage gene signature. Patients were divided into high-risk and low-risk groups using the median EMGS score, with the high-risk group showing significantly worse survival. This group also demonstrated upregulated pathways associated with tumor progression, such as epithelial-mesenchymal transition and angiogenesis, and downregulated metabolic pathways. Moreover, the high-risk group presented an immunosuppressive microenvironment, with a higher TIDE score indicating lower effectiveness of immunotherapy. The study identifies potential drugs targeting the high-risk group, suggesting therapeutic avenues to improve survival. Conclusively, the EMGS score identifies colorectal cancer patients at high risk of liver metastases, highlighting the role of specific macrophage subsets in tumor progression and providing a basis for personalized treatment strategies.

摘要

本研究通过鉴定不同的巨噬细胞亚群,开发了一种预测结直肠癌肝转移转移和预后的预后模型。使用来自原发性结直肠癌和肝转移的 scRNA-seq 数据,我们剖析了细胞景观,以发现独特的巨噬细胞亚群,特别是在肝转移中普遍存在的 EEF1G+巨噬细胞。该研究利用 GSE231559、TCGA 和 GEO 数据库中的数据,根据 EEF1G+巨噬细胞基因特征构建了一个名为 EMGS 的 8 基因风险模型。患者根据 EMGS 评分的中位数分为高风险和低风险组,高风险组的生存明显更差。该组还表现出与肿瘤进展相关的上调途径,如上皮-间充质转化和血管生成,以及下调的代谢途径。此外,高风险组表现出免疫抑制的微环境,较高的 TIDE 评分表明免疫治疗的效果较低。该研究确定了针对高风险组的潜在药物,为提高生存率提供了治疗途径。总之,EMGS 评分确定了结直肠癌患者肝转移的高风险,突出了特定巨噬细胞亚群在肿瘤进展中的作用,并为个性化治疗策略提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/f320823fbe5b/41598_2024_77248_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/ea4c71023d71/41598_2024_77248_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/97af8c78d4cf/41598_2024_77248_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/feb90c28d289/41598_2024_77248_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/7219aab83816/41598_2024_77248_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/0ebc5f505b71/41598_2024_77248_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/da7c69fa32c7/41598_2024_77248_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/f320823fbe5b/41598_2024_77248_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/ea4c71023d71/41598_2024_77248_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/97af8c78d4cf/41598_2024_77248_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/feb90c28d289/41598_2024_77248_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/7219aab83816/41598_2024_77248_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/0ebc5f505b71/41598_2024_77248_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/da7c69fa32c7/41598_2024_77248_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aef8/11530676/f320823fbe5b/41598_2024_77248_Fig7_HTML.jpg

相似文献

1
Characterization of metastasis-specific macrophages in colorectal cancer for prognosis prediction and immunometabolic remodeling.结直肠癌中转移相关巨噬细胞的特征分析用于预后预测和免疫代谢重塑。
Sci Rep. 2024 Nov 1;14(1):26361. doi: 10.1038/s41598-024-77248-2.
2
Comprehensive scRNA-seq analysis to identify new markers of M2 macrophages for predicting the prognosis of prostate cancer.综合单细胞 RNA 测序分析鉴定 M2 巨噬细胞的新标志物用于预测前列腺癌的预后。
Ann Med. 2024 Dec;56(1):2398195. doi: 10.1080/07853890.2024.2398195. Epub 2024 Sep 2.
3
Crosstalk between cancer cells and tumor associated macrophages is required for mesenchymal circulating tumor cell-mediated colorectal cancer metastasis.癌细胞与肿瘤相关巨噬细胞之间的串扰对于间质循环肿瘤细胞介导的结直肠癌转移是必需的。
Mol Cancer. 2019 Mar 30;18(1):64. doi: 10.1186/s12943-019-0976-4.
4
Metastasis and basement membrane-related signature enhances hepatocellular carcinoma prognosis and diagnosis by integrating single-cell RNA sequencing analysis and immune microenvironment assessment.转移和基底膜相关特征通过整合单细胞RNA测序分析和免疫微环境评估增强肝细胞癌的预后和诊断。
J Transl Med. 2024 Jul 31;22(1):711. doi: 10.1186/s12967-024-05493-0.
5
Establishment of a chemokine-based prognostic model and identification of CXCL10+ M1 macrophages as predictors of neoadjuvant therapy efficacy in colorectal cancer.建立基于趋化因子的预后模型,并鉴定 CXCL10+M1 巨噬细胞作为结直肠癌新辅助治疗疗效的预测因子。
Front Immunol. 2024 Aug 7;15:1400722. doi: 10.3389/fimmu.2024.1400722. eCollection 2024.
6
A Novel TGF-β-Related Signature for Predicting Prognosis, Tumor Microenvironment, and Therapeutic Response in Colorectal Cancer.一种新型 TGF-β 相关标志物用于预测结直肠癌的预后、肿瘤微环境和治疗反应。
Biochem Genet. 2024 Aug;62(4):2999-3029. doi: 10.1007/s10528-023-10591-7. Epub 2023 Dec 7.
7
Exosome-encapsulated miRNAs contribute to CXCL12/CXCR4-induced liver metastasis of colorectal cancer by enhancing M2 polarization of macrophages.外泌体包裹的 miRNA 通过增强巨噬细胞的 M2 极化促进结直肠癌 CXCL12/CXCR4 诱导的肝转移。
Cancer Lett. 2020 Apr 1;474:36-52. doi: 10.1016/j.canlet.2020.01.005. Epub 2020 Jan 10.
8
SERPINC1, a new prognostic predictor of colon cancer, promote colon cancer progression through EMT.SERPINC1,一种新的结肠癌预后预测因子,通过 EMT 促进结肠癌的进展。
Cancer Rep (Hoboken). 2024 Jun;7(6):e2079. doi: 10.1002/cnr2.2079.
9
Tumor cell-derived SPON2 promotes M2-polarized tumor-associated macrophage infiltration and cancer progression by activating PYK2 in CRC.肿瘤细胞来源的 SPON2 通过激活 CRC 中的 PYK2 促进 M2 极化的肿瘤相关巨噬细胞浸润和癌症进展。
J Exp Clin Cancer Res. 2021 Sep 28;40(1):304. doi: 10.1186/s13046-021-02108-0.
10
CPEB3 inhibits epithelial-mesenchymal transition by disrupting the crosstalk between colorectal cancer cells and tumor-associated macrophages via IL-6R/STAT3 signaling.CPEB3 通过阻断结直肠癌细胞与肿瘤相关巨噬细胞之间的细胞因子信号转导及转录激活因子 3(IL-6R/STAT3)信号通路来抑制上皮-间质转化。
J Exp Clin Cancer Res. 2020 Jul 11;39(1):132. doi: 10.1186/s13046-020-01637-4.

引用本文的文献

1
Exploring macrophage polarization as a prognostic indicator for colorectal cancer: Unveiling the impact of metalloproteinase mutations.探索巨噬细胞极化作为结直肠癌的预后指标:揭示金属蛋白酶突变的影响。
World J Clin Cases. 2025 Aug 16;13(23):105011. doi: 10.12998/wjcc.v13.i23.105011.
2
Construction of Gene Regulatory Networks Based on Spatial Multi-Omics Data and Application in Tumor-Boundary Analysis.基于空间多组学数据的基因调控网络构建及其在肿瘤边界分析中的应用
Genes (Basel). 2025 Jul 13;16(7):821. doi: 10.3390/genes16070821.

本文引用的文献

1
Sirpα on tumor-associated myeloid cells restrains antitumor immunity in colorectal cancer independent of its interaction with CD47.Sirpα 抑制结直肠癌肿瘤相关髓系细胞的抗肿瘤免疫,与 CD47 无关。
Nat Cancer. 2024 Mar;5(3):500-516. doi: 10.1038/s43018-023-00691-z. Epub 2024 Jan 10.
2
Single-cell transcriptomic analysis deciphers heterogenous cancer stem-like cells in colorectal cancer and their organ-specific metastasis.单细胞转录组分析揭示结直肠癌中异质性癌症干细胞样细胞及其器官特异性转移。
Gut. 2024 Feb 23;73(3):470-484. doi: 10.1136/gutjnl-2023-330243.
3
Oncogenic KRAS Drives Lipofibrogenesis to Promote Angiogenesis and Colon Cancer Progression.
致癌性 KRAS 驱动脂肪纤维生成以促进血管生成和结肠癌进展。
Cancer Discov. 2023 Dec 12;13(12):2652-2673. doi: 10.1158/2159-8290.CD-22-1467.
4
Characterizing cancer metabolism from bulk and single-cell RNA-seq data using METAFlux.使用 METAFlux 从批量和单细胞 RNA-seq 数据中描绘癌症代谢。
Nat Commun. 2023 Aug 12;14(1):4883. doi: 10.1038/s41467-023-40457-w.
5
Single-cell and spatial transcriptome analysis reveals the cellular heterogeneity of liver metastatic colorectal cancer.单细胞和空间转录组分析揭示了肝转移性结直肠癌的细胞异质性。
Sci Adv. 2023 Jun 16;9(24):eadf5464. doi: 10.1126/sciadv.adf5464.
6
Methotrexate Provokes Disparate Folate Metabolism Gene Expression and Alternative Splicing in Ex Vivo Monocytes and GM-CSF- and M-CSF-Polarized Macrophages.甲氨蝶呤诱导体外单核细胞和 GM-CSF 及 M-CSF 极化巨噬细胞中差异叶酸代谢基因表达和选择性剪接。
Int J Mol Sci. 2023 Jun 1;24(11):9641. doi: 10.3390/ijms24119641.
7
Targeting IRG1 reverses the immunosuppressive function of tumor-associated macrophages and enhances cancer immunotherapy.靶向 IRG1 可逆转肿瘤相关巨噬细胞的免疫抑制功能,并增强癌症免疫治疗。
Sci Adv. 2023 Apr 28;9(17):eadg0654. doi: 10.1126/sciadv.adg0654.
8
An immunometabolism subtyping system identifies S100A9 macrophage as an immune therapeutic target in colorectal cancer based on multiomics analysis.基于多组学分析的免疫代谢亚型系统确定 S100A9 巨噬细胞为结直肠癌的免疫治疗靶点。
Cell Rep Med. 2023 Apr 18;4(4):100987. doi: 10.1016/j.xcrm.2023.100987. Epub 2023 Mar 28.
9
Survival rate of colorectal cancer in China: A systematic review and meta-analysis.中国结直肠癌的生存率:一项系统评价与荟萃分析。
Front Oncol. 2023 Mar 3;13:1033154. doi: 10.3389/fonc.2023.1033154. eCollection 2023.
10
Survival improvement for patients with metastatic colorectal cancer over twenty years.二十年来转移性结直肠癌患者的生存改善情况。
NPJ Precis Oncol. 2023 Feb 13;7(1):16. doi: 10.1038/s41698-023-00353-4.