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Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1
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 i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040068/ https://www.ncbi.nlm.nih.gov/pubmed/33889273 http://dx.doi.org/10.4251/wjgo.v13.i4.216 |
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author | Sun, Ke-Ran Lv, Hui-Fang Chen, Bei-Bei Nie, Cai-Yun Zhao, Jing Chen, Xiao-Bing |
author_facet | Sun, Ke-Ran Lv, Hui-Fang Chen, Bei-Bei Nie, Cai-Yun Zhao, Jing Chen, Xiao-Bing |
author_sort | Sun, Ke-Ran |
collection | PubMed |
description | 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 in vitro. 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. |
format | Online Article Text |
id | pubmed-8040068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-80400682021-04-21 Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 Sun, Ke-Ran Lv, Hui-Fang Chen, Bei-Bei Nie, Cai-Yun Zhao, Jing Chen, Xiao-Bing World J Gastrointest Oncol Minireviews 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 in vitro. 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. Baishideng Publishing Group Inc 2021-04-15 2021-04-15 /pmc/articles/PMC8040068/ /pubmed/33889273 http://dx.doi.org/10.4251/wjgo.v13.i4.216 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Minireviews Sun, Ke-Ran Lv, Hui-Fang Chen, Bei-Bei Nie, Cai-Yun Zhao, Jing Chen, Xiao-Bing Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 |
title | Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 |
title_full | Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 |
title_fullStr | Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 |
title_full_unstemmed | Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 |
title_short | Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1 |
title_sort | latest therapeutic target for gastric cancer: anthrax toxin receptor 1 |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040068/ https://www.ncbi.nlm.nih.gov/pubmed/33889273 http://dx.doi.org/10.4251/wjgo.v13.i4.216 |
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