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Gene Regulation and Targeted Therapy in Gastric Cancer Peritoneal Metastasis: Radiological Findings from Dual Energy CT and PET/CT
Published on: January 22, 2018
Latest therapeutic target for gastric cancer: Anthrax toxin receptor 1
Ke-Ran Sun1, Hui-Fang Lv1, Bei-Bei Chen1
1Department of Oncology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450000, Henan Province, China.
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 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.
Insights
Anthrax toxin receptor 1 (ANTXR1) is crucial for tumor angiogenesis and growth, but not essential for normal physiological processes. Targeting ANTXR1 shows promise for inhibiting tumor progression.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Anthrax toxin receptor 1 (ANTXR1), also known as tumor endothelial marker 8, is a cell surface protein found on tumor-infiltrating vessels.
- ANTXR1 is overexpressed in various human and mouse tumors, including gastric, lung, intestinal, and breast cancer.
- While its physiological role is unclear, ANTXR1 binds collagen and aids endothelial cell migration in vitro.
Purpose of the Study:
- To review the physiological functions of ANTXR1.
- To explore the role of ANTXR1 in tumor angiogenesis, growth, and metastasis.
- To summarize findings on ANTXR1's necessity for tumor-specific angiogenesis.
Main Methods:
- Review of existing literature on ANTXR1.
- Analysis of ANTXR1 expression in different tumor types.
- Examination of ANTXR1 knockout mouse models for developmental and tumor growth phenotypes.
Main Results:
- ANTXR1 knockout mice exhibit impaired melanoma growth, suggesting a role in tumor progression.
- ANTXR1 is upregulated in tumor vasculature and sometimes in tumor cells.
- Developmental angiogenesis and wound healing are unaffected in ANTXR1 knockout mice.
- Host-derived ANTXR1 promotes tumor growth, potentially via immune interactions.
- ANTXR1 appears essential for tumor angiogenesis, not physiological angiogenesis.
Conclusions:
- ANTXR1 is a key player in tumor angiogenesis and progression.
- Targeting ANTXR1, through vaccines or toxin inhibition, may offer therapeutic strategies for cancer.
- ANTXR1 represents a promising target for anti-cancer therapies focused on angiogenesis inhibition.
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