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肿瘤相关巨噬细胞——对分子肿瘤学和成像的影响

Tumor-Associated Macrophages-Implications for Molecular Oncology and Imaging.

作者信息

Kimm Melanie A, Klenk Christopher, Alunni-Fabbroni Marianna, Kästle Sophia, Stechele Matthias, Ricke Jens, Eisenblätter Michel, Wildgruber Moritz

机构信息

Department of Radiology, University Hospital, LMU Munich, 81377 Munich, Germany.

Department of Diagnostic and Interventional Radiology, Freiburg University Hospital, 79106 Freiburg, Germany.

出版信息

Biomedicines. 2021 Apr 2;9(4):374. doi: 10.3390/biomedicines9040374.

DOI:10.3390/biomedicines9040374
PMID:33918295
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8066018/
Abstract

Tumor-associated macrophages (TAMs) represent the largest group of leukocytes within the tumor microenvironment (TME) of solid tumors and orchestrate the composition of anti- as well as pro-tumorigenic factors. This makes TAMs an excellent target for novel cancer therapies. The plasticity of TAMs resulting in varying membrane receptors and expression of intracellular proteins allow the specific characterization of different subsets of TAMs. Those markers similarly allow tracking of TAMs by different means of molecular imaging. This review aims to provides an overview of the origin of tumor-associated macrophages, their polarization in different subtypes, and how characteristic markers of the subtypes can be used as targets for molecular imaging and theranostic approaches.

摘要

肿瘤相关巨噬细胞(TAM)是实体瘤肿瘤微环境(TME)中最大的白细胞群体,可协调抗肿瘤和促肿瘤发生因子的组成。这使得TAM成为新型癌症治疗的理想靶点。TAM的可塑性导致其膜受体和细胞内蛋白质表达各异,从而能够对不同亚群的TAM进行特异性表征。这些标志物同样有助于通过不同的分子成像手段追踪TAM。本综述旨在概述肿瘤相关巨噬细胞的起源、它们向不同亚型的极化过程,以及这些亚型的特征性标志物如何用作分子成像和诊疗方法的靶点。

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本文引用的文献

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S100A9-Imaging Enables Estimation of Early Therapy-Mediated Changes in the Inflammatory Tumor Microenvironment.S100A9成像有助于评估早期治疗介导的炎症性肿瘤微环境变化。
Biomedicines. 2021 Jan 3;9(1):29. doi: 10.3390/biomedicines9010029.
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Distinct Populations of Immune-Suppressive Macrophages Differentiate from Monocytic Myeloid-Derived Suppressor Cells in Cancer.肿瘤中免疫抑制性巨噬细胞的不同群体来源于单核细胞来源的髓系抑制细胞。
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Analyzing One Cell at a TIME: Analysis of Myeloid Cell Contributions in the Tumor Immune Microenvironment.
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Antagonistic action of GPS2 and KDM1A at enhancers governs alternative macrophage activation by interleukin 4.GPS2 和 KDM1A 在增强子上的拮抗作用通过白细胞介素 4 调控巨噬细胞的选择性激活。
Nucleic Acids Res. 2023 Feb 22;51(3):1067-1086. doi: 10.1093/nar/gkac1230.
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Early monocyte response following local ablation in hepatocellular carcinoma.肝细胞癌局部消融后的早期单核细胞反应
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Engineering Macrophages Nanotechnology and Genetic Manipulation for Cancer Therapy.工程化巨噬细胞:用于癌症治疗的纳米技术与基因操纵
Front Oncol. 2022 Jan 6;11:786913. doi: 10.3389/fonc.2021.786913. eCollection 2021.
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