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胃肠道肿瘤微环境。

The gastrointestinal tumor microenvironment.

机构信息

II. Medizinische Klinik, Klinikum rechts der Isar, Technische Universität München, München, Germany.

Institut für Molekulare Immunologie, Klinikum rechts der Isar, Technische Universität München, München, Germany.

出版信息

Gastroenterology. 2013 Jul;145(1):63-78. doi: 10.1053/j.gastro.2013.03.052. Epub 2013 Apr 10.

DOI:10.1053/j.gastro.2013.03.052
PMID:23583733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4012393/
Abstract

Over the past decade, the microenvironment of gastrointestinal tumors has gained increasing attention because it is required for tumor initiation, progression, and metastasis. The tumor microenvironment has many components and has been recognized as one of the major hallmarks of epithelial cancers. Although therapeutic strategies for gastrointestinal cancer have previously focused on the epithelial cell compartment, there is increasing interest in reagents that alter the microenvironment, based on reported interactions among gastrointestinal epithelial, stromal, and immune cells during gastrointestinal carcinogenesis. We review the different cellular components of the gastrointestinal tumor microenvironment and their functions in carcinogenesis and discuss how improving our understanding of the complex stromal network could lead to new therapeutic strategies.

摘要

在过去的十年中,胃肠道肿瘤的微环境越来越受到关注,因为它是肿瘤发生、进展和转移所必需的。肿瘤微环境有许多组成部分,已被认为是上皮癌的主要特征之一。尽管胃肠道癌的治疗策略以前集中在上皮细胞区室,但基于胃肠道上皮细胞、基质和免疫细胞在胃肠道癌变过程中的相互作用的报道,人们对改变微环境的试剂越来越感兴趣。我们回顾了胃肠道肿瘤微环境的不同细胞成分及其在癌变中的功能,并讨论了如何加深对复杂基质网络的理解可能导致新的治疗策略。

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The gastrointestinal tumor microenvironment.胃肠道肿瘤微环境。
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Potential therapeutic targets in myeloid cell therapy for overcoming chemoresistance and immune suppression in gastrointestinal tumors.在用于克服胃肠道肿瘤化疗耐药和免疫抑制的髓系细胞治疗中潜在的治疗靶点。
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Dual regulation of gastrointestinal tumor progression by the IFN-γ/STAT1 pathway and prospects for targeted therapy.IFN-γ/STAT1通路对胃肠道肿瘤进展的双重调控及靶向治疗前景
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本文引用的文献

1
Intestinal tumorigenesis initiated by dedifferentiation and acquisition of stem-cell-like properties.肠肿瘤发生由去分化和获得干细胞样特性引发。
Cell. 2013 Jan 17;152(1-2):25-38. doi: 10.1016/j.cell.2012.12.012. Epub 2012 Dec 27.
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Loss of p53 in enterocytes generates an inflammatory microenvironment enabling invasion and lymph node metastasis of carcinogen-induced colorectal tumors.肠上皮细胞中 p53 的缺失会产生炎症微环境,从而使致癌物诱导的结直肠肿瘤发生侵袭和淋巴结转移。
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Dclk1 distinguishes between tumor and normal stem cells in the intestine.
mRNA vaccines for gastrointestinal cancers: a paradigm shift in treatment.
用于胃肠道癌症的mRNA疫苗:治疗领域的范式转变
Naunyn Schmiedebergs Arch Pharmacol. 2025 Aug 6. doi: 10.1007/s00210-025-04462-8.
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Macrophages foster anti-tumor immunity by ZEB1-dependent cytotoxic T cell chemoattraction.巨噬细胞通过ZEB1依赖的细胞毒性T细胞趋化作用促进抗肿瘤免疫。
Commun Biol. 2025 Jul 1;8(1):976. doi: 10.1038/s42003-025-08339-7.
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Editorial: Targeting the tumor microenvironment for effective treatment of gastrointestinal cancers.社论:靶向肿瘤微环境以有效治疗胃肠道癌症
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The Role of Inflammation in Cancer: Mechanisms of Tumor Initiation, Progression, and Metastasis.炎症在癌症中的作用:肿瘤起始、进展和转移的机制
Cells. 2025 Mar 25;14(7):488. doi: 10.3390/cells14070488.
7
Identifying distinct prognostic and predictive contributions of tumor epithelium versus tumor microenvironment in colorectal cancer.确定肿瘤上皮与肿瘤微环境在结直肠癌中的不同预后和预测作用。
BMC Cancer. 2025 Mar 12;25(1):441. doi: 10.1186/s12885-025-13829-2.
8
Translating CD47-targeted therapy in gastrointestinal cancers: Insights from preclinical to clinical studies.胃肠道癌症中CD47靶向治疗的转化:从临床前研究到临床研究的见解
iScience. 2024 Nov 26;27(12):111478. doi: 10.1016/j.isci.2024.111478. eCollection 2024 Dec 20.
9
Microenvironment and Biomarkers in Esophageal Cancers: An Approach for Early Detection and Identification.食管癌中的微环境与生物标志物:早期检测与识别方法
Cureus. 2024 Nov 22;16(11):e74242. doi: 10.7759/cureus.74242. eCollection 2024 Nov.
10
Oxidative Stress and Cancer Therapy: Controlling Cancer Cells Using Reactive Oxygen Species.氧化应激与癌症治疗:利用活性氧物质控制癌细胞。
Int J Mol Sci. 2024 Nov 18;25(22):12387. doi: 10.3390/ijms252212387.
Dclk1 区分肠道中的肿瘤和正常干细胞。
Nat Genet. 2013 Jan;45(1):98-103. doi: 10.1038/ng.2481. Epub 2012 Dec 2.
4
Lysyl oxidase plays a critical role in endothelial cell stimulation to drive tumor angiogenesis.赖氨酰氧化酶在刺激内皮细胞以驱动肿瘤血管生成方面发挥着关键作用。
Cancer Res. 2013 Jan 15;73(2):583-94. doi: 10.1158/0008-5472.CAN-12-2447. Epub 2012 Nov 27.
5
Bevacizumab plus oxaliplatin-based chemotherapy as adjuvant treatment for colon cancer (AVANT): a phase 3 randomised controlled trial.贝伐珠单抗联合奥沙利铂为基础的化疗作为结肠癌的辅助治疗(AVANT):一项 3 期随机对照临床试验。
Lancet Oncol. 2012 Dec;13(12):1225-33. doi: 10.1016/S1470-2045(12)70509-0. Epub 2012 Nov 16.
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Inflammation and colorectal cancer: colitis-associated neoplasia.炎症与结直肠癌:结肠炎相关肿瘤。
Semin Immunopathol. 2013 Mar;35(2):229-44. doi: 10.1007/s00281-012-0352-6. Epub 2012 Nov 16.
7
Dependency of colorectal cancer on a TGF-β-driven program in stromal cells for metastasis initiation.结直肠癌依赖于基质细胞中 TGF-β 驱动的程序进行转移起始。
Cancer Cell. 2012 Nov 13;22(5):571-84. doi: 10.1016/j.ccr.2012.08.013.
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Aspirin use, tumor PIK3CA mutation, and colorectal-cancer survival.阿司匹林使用、肿瘤 PIK3CA 突变与结直肠癌生存
N Engl J Med. 2012 Oct 25;367(17):1596-606. doi: 10.1056/NEJMoa1207756.
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STAT3-driven upregulation of TLR2 promotes gastric tumorigenesis independent of tumor inflammation.STAT3 驱动的 TLR2 上调促进了肿瘤炎症以外的胃癌发生。
Cancer Cell. 2012 Oct 16;22(4):466-78. doi: 10.1016/j.ccr.2012.08.010.
10
The distribution of macrophages with a M1 or M2 phenotype in relation to prognosis and the molecular characteristics of colorectal cancer.M1 型和 M2 型巨噬细胞在结直肠癌中的分布与预后及分子特征的关系。
PLoS One. 2012;7(10):e47045. doi: 10.1371/journal.pone.0047045. Epub 2012 Oct 15.