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胃癌的最新治疗靶点:炭疽毒素受体1。

Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1.

作者信息

Sun Ke-Ran, Lv Hui-Fang, Chen Bei-Bei, Nie Cai-Yun, Zhao Jing, Chen Xiao-Bing

机构信息

Department of Oncology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450000, Henan Province, China.

出版信息

World J Gastrointest Oncol. 2021 Apr 15;13(4):216-222. doi: 10.4251/wjgo.v13.i4.216.

DOI:10.4251/wjgo.v13.i4.216
PMID:33889273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8040068/
Abstract

Anthrax toxin receptor 1 (ANTXR1), also known as tumor endothelial marker 8, is a highly conserved cell surface protein overexpressed in tumor-infiltrating vessels. It was first found in vascular endothelial cells of human colorectal cancer. Although our understanding of its physiological function is limited, it has been found that ANTXR1 binds collagen and promotes migration of endothelial cells . ANTXR1 is upregulated in vessels of different tumor types in mice and humans, and is also expressed by tumor cells themselves in some tumors, such as gastric, lung, intestinal and breast cancer. Developmental angiogenesis and wound healing were not disturbed in ANTXR1 knockout mice, but compared with wild-type mice, growth of melanoma was impaired after ANTXR1 knockout, indicating that host-derived ANTXR1 can promote tumor growth on the basis of immune activity. Previous studies have shown that ANTXR1 vaccines or sublethal doses of anthrax toxin can inhibit angiogenesis, slow tumor growth and prolong survival. These studies suggest that ANTXR1 is necessary for tumor rather than physiological angiogenesis. It has been found that ANTXR1 plays an important role in tumor angiogenesisas well as in the growth and metastasis of many kinds of tumors. This article reviews the physiological function of ANTXR1 and its role in different kinds of cancer.

摘要

炭疽毒素受体1(ANTXR1),也被称为肿瘤内皮标志物8,是一种在肿瘤浸润血管中过度表达的高度保守的细胞表面蛋白。它最初在人类结直肠癌的血管内皮细胞中被发现。尽管我们对其生理功能的了解有限,但已发现ANTXR1能结合胶原蛋白并促进内皮细胞迁移。在小鼠和人类的不同肿瘤类型的血管中,ANTXR1表达上调,并且在一些肿瘤(如胃癌、肺癌、肠癌和乳腺癌)中肿瘤细胞自身也表达ANTXR1。在ANTXR1基因敲除小鼠中,发育性血管生成和伤口愈合未受干扰,但与野生型小鼠相比,ANTXR1基因敲除后黑色素瘤的生长受到损害,这表明宿主来源的ANTXR1在免疫活性的基础上可促进肿瘤生长。先前的研究表明,ANTXR1疫苗或亚致死剂量的炭疽毒素可抑制血管生成、减缓肿瘤生长并延长生存期。这些研究表明,ANTXR1对肿瘤血管生成而非生理性血管生成是必需的。已发现ANTXR1在肿瘤血管生成以及多种肿瘤的生长和转移中起重要作用。本文综述了ANTXR1的生理功能及其在不同类型癌症中的作用。

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Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1.胃癌的最新治疗靶点:炭疽毒素受体1。
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2
Anthrax toxin receptor 1/tumor endothelial marker 8 promotes gastric cancer progression through activation of the PI3K/AKT/mTOR signaling pathway.炭疽毒素受体 1/肿瘤内皮标志物 8 通过激活 PI3K/AKT/mTOR 信号通路促进胃癌进展。
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Anthrax Toxin Receptor 1 Is Essential for Arteriogenesis in a Mouse Model of Hindlimb Ischemia.炭疽毒素受体1对后肢缺血小鼠模型中的动脉生成至关重要。
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Cells. 2023 Nov 14;12(22):2623. doi: 10.3390/cells12222623.
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AB Toxins as High-Affinity Ligands for Cell Targeting in Cancer Therapy.AB 毒素作为癌症治疗中细胞靶向的高亲和力配体。
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本文引用的文献

1
Antxr1, Which is a Target of Runx2, Regulates Chondrocyte Proliferation and Apoptosis.Antxr1 是 Runx2 的靶点,调节软骨细胞增殖和凋亡。
Int J Mol Sci. 2020 Mar 31;21(7):2425. doi: 10.3390/ijms21072425.
2
The relationship between TEM8 and early diagnosis and prognosis of lung cancer.肿瘤内皮标志物8(TEM8)与肺癌早期诊断及预后的关系
Minerva Med. 2021 Jun;112(3):359-364. doi: 10.23736/S0026-4806.20.06444-7. Epub 2020 Mar 12.
3
Anthrax toxin receptor 1/tumor endothelial marker 8 promotes gastric cancer progression through activation of the PI3K/AKT/mTOR signaling pathway.炭疽毒素受体 1/肿瘤内皮标志物 8 通过激活 PI3K/AKT/mTOR 信号通路促进胃癌进展。
Cancer Sci. 2020 Apr;111(4):1132-1145. doi: 10.1111/cas.14326. Epub 2020 Feb 19.
4
ANTXR1 (TEM8) overexpression in gastric adenocarcinoma makes the protein a potential target of immunotherapy.在胃腺癌中,ANTXR1(TEM8)的过表达使该蛋白成为免疫治疗的潜在靶点。
Cancer Immunol Immunother. 2019 Oct;68(10):1597-1603. doi: 10.1007/s00262-019-02392-y. Epub 2019 Sep 14.
5
Converging physiological roles of the anthrax toxin receptors.炭疽毒素受体的趋同生理作用。
F1000Res. 2019 Aug 12;8. doi: 10.12688/f1000research.19423.1. eCollection 2019.
6
Chemo-resistant Gastric Cancer Associated Gene Expression Signature: Bioinformatics Analysis Based on Gene Expression Omnibus.化疗耐药性胃癌相关基因表达特征:基于基因表达综合数据库的生物信息学分析
Anticancer Res. 2019 Apr;39(4):1689-1698. doi: 10.21873/anticanres.13274.
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Seneca Valley Virus Exploits TEM8, a Collagen Receptor Implicated in Tumor Growth.塞内卡山谷病毒利用TEM8,一种与肿瘤生长有关的胶原蛋白受体。
Front Oncol. 2018 Nov 6;8:506. doi: 10.3389/fonc.2018.00506. eCollection 2018.
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MSLN (Mesothelin), ANTXR1 (TEM8), and MUC3A are the potent antigenic targets for CAR T cell therapy of gastric adenocarcinoma.MSLN(间皮素)、ANTXR1(TEM8)和 MUC3A 是胃腺癌 CAR T 细胞治疗的有效抗原靶点。
J Cell Biochem. 2019 Apr;120(4):5010-5017. doi: 10.1002/jcb.27776. Epub 2018 Sep 27.
9
TEM8 functions as a receptor for uPA and mediates uPA-stimulated EGFR phosphorylation.TEM8 作为 uPA 的受体发挥作用,并介导 uPA 刺激的 EGFR 磷酸化。
Cell Commun Signal. 2018 Sep 21;16(1):62. doi: 10.1186/s12964-018-0272-8.
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