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Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma
Endosialin/CD248/tumor endothelial marker 1 is classified as a C-type lectin-like transmembrane receptor, found on the plasma membrane of activated mesenchymal cells, which binds to fibronectin. Although endosialin is expressed at high levels in stem-like cells of sarcomas, its role has not been ful...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674875/ https://www.ncbi.nlm.nih.gov/pubmed/34976154 http://dx.doi.org/10.3892/ol.2021.13160 |
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author | Kondo, Yumiko Honoki, Kanya Kishi, Shingo Mori, Shiori Fujiwara-Tani, Rina Tsukamoto, Shinji Fujii, Hiromasa Kuniyasu, Hiroki Tanaka, Yasuhito |
author_facet | Kondo, Yumiko Honoki, Kanya Kishi, Shingo Mori, Shiori Fujiwara-Tani, Rina Tsukamoto, Shinji Fujii, Hiromasa Kuniyasu, Hiroki Tanaka, Yasuhito |
author_sort | Kondo, Yumiko |
collection | PubMed |
description | Endosialin/CD248/tumor endothelial marker 1 is classified as a C-type lectin-like transmembrane receptor, found on the plasma membrane of activated mesenchymal cells, which binds to fibronectin. Although endosialin is expressed at high levels in stem-like cells of sarcomas, its role has not been fully uncovered. The present study aimed to determine whether endosialin expression is associated with tumor progression and metastasis, and whether endosialin has the potential to act as a novel therapeutic target in osteosarcoma (OS) using MORAb-004/ontuxizumab, a humanized monoclonal antibody, which targets the type C lectin domain of endosialin. The results demonstrated that endosialin was highly expressed in OSs with metastatic disease. Furthermore, MORAb-004 had no cytostatic effect on OS cells in vitro and did not change the expression of stem cells and differentiation markers; however, it inhibited migration of OS cells. Taken together, these results suggest that endosialin may play a role in migration, and may be involved in the metastatic process of OSs. Furthermore, MORAb-004 reduces the motility of OS cells, and suppresses invasion and the development of metastatic lesions. |
format | Online Article Text |
id | pubmed-8674875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-86748752021-12-30 Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma Kondo, Yumiko Honoki, Kanya Kishi, Shingo Mori, Shiori Fujiwara-Tani, Rina Tsukamoto, Shinji Fujii, Hiromasa Kuniyasu, Hiroki Tanaka, Yasuhito Oncol Lett Articles Endosialin/CD248/tumor endothelial marker 1 is classified as a C-type lectin-like transmembrane receptor, found on the plasma membrane of activated mesenchymal cells, which binds to fibronectin. Although endosialin is expressed at high levels in stem-like cells of sarcomas, its role has not been fully uncovered. The present study aimed to determine whether endosialin expression is associated with tumor progression and metastasis, and whether endosialin has the potential to act as a novel therapeutic target in osteosarcoma (OS) using MORAb-004/ontuxizumab, a humanized monoclonal antibody, which targets the type C lectin domain of endosialin. The results demonstrated that endosialin was highly expressed in OSs with metastatic disease. Furthermore, MORAb-004 had no cytostatic effect on OS cells in vitro and did not change the expression of stem cells and differentiation markers; however, it inhibited migration of OS cells. Taken together, these results suggest that endosialin may play a role in migration, and may be involved in the metastatic process of OSs. Furthermore, MORAb-004 reduces the motility of OS cells, and suppresses invasion and the development of metastatic lesions. D.A. Spandidos 2022-02 2021-12-06 /pmc/articles/PMC8674875/ /pubmed/34976154 http://dx.doi.org/10.3892/ol.2021.13160 Text en Copyright: © Kondo et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Kondo, Yumiko Honoki, Kanya Kishi, Shingo Mori, Shiori Fujiwara-Tani, Rina Tsukamoto, Shinji Fujii, Hiromasa Kuniyasu, Hiroki Tanaka, Yasuhito Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
title | Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
title_full | Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
title_fullStr | Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
title_full_unstemmed | Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
title_short | Endosialin/CD248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
title_sort | endosialin/cd248 may be a potential therapeutic target to prevent the invasion and metastasis in osteosarcoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674875/ https://www.ncbi.nlm.nih.gov/pubmed/34976154 http://dx.doi.org/10.3892/ol.2021.13160 |
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