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Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study
BACKGROUND: Osteosarcoma (OS) is a common malignant bone tumor with poor prognosis. We previously reviewed that CD146 is correlated with multiple cancer progression, while its impact on OS is currently not systematically studied. METHODS: MG63 was transfected with lentivirus to express CD146 ectopic...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186124/ https://www.ncbi.nlm.nih.gov/pubmed/34103063 http://dx.doi.org/10.1186/s12935-021-02006-7 |
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author | Lei, Xing Wang, Kewei Wang, Wenbo Jin, Hao Gu, Wenguang Chen, Zhiguo Wang, Wei Gao, Kaituo Wang, Huan |
author_facet | Lei, Xing Wang, Kewei Wang, Wenbo Jin, Hao Gu, Wenguang Chen, Zhiguo Wang, Wei Gao, Kaituo Wang, Huan |
author_sort | Lei, Xing |
collection | PubMed |
description | BACKGROUND: Osteosarcoma (OS) is a common malignant bone tumor with poor prognosis. We previously reviewed that CD146 is correlated with multiple cancer progression, while its impact on OS is currently not systematically studied. METHODS: MG63 was transfected with lentivirus to express CD146 ectopically, and anti-CD146 neutralizing antibody ab75769 was used to inhibit 143B. Cyclic migration of MG63 and co-culture between MG63 and 143B were used to explore the role of OS malignancy in CD146 expression. The effect of OS cell medium (CM) on endothelium behaviors was assessed, and the expression changes of CD146 before and after co-culture of endothelium and OS were evaluated. Finally, the expression of CD146 in OS was detected under different culture conditions, including hyperoxia, low oxygen, high glucose and low glucose conditions. RESULTS: CD146 promoted the colony formation, migration, invasion and homotypic adhesion of OS cells, and reducing the concentration of soluble CD146 in the OS medium inhibited the proliferation, migration and lumen formation of the cultured endothelium. However, CD146 did not affect the adhesion between OS and endothelium, nor did co-culture of both sides affect the CD146 expression. Similarly, the proliferation, migration and CD146 expression of MG63 remained unchanged after many cycles of migration itself, as did its co-culture with 143B for expressing CD146. In addition, we also showed that high glucose promoted the expression of CD146 in OS, while hypoxia had the opposite effect. CONCLUSIONS: These findings demonstrate that CD146 promotes OS progression by mediating pro-tumoral and angiogenic effects. Thus, CD146 could be a potential therapeutic target for OS, especially for OS patients with diabetes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02006-7. |
format | Online Article Text |
id | pubmed-8186124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81861242021-06-10 Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study Lei, Xing Wang, Kewei Wang, Wenbo Jin, Hao Gu, Wenguang Chen, Zhiguo Wang, Wei Gao, Kaituo Wang, Huan Cancer Cell Int Primary Research BACKGROUND: Osteosarcoma (OS) is a common malignant bone tumor with poor prognosis. We previously reviewed that CD146 is correlated with multiple cancer progression, while its impact on OS is currently not systematically studied. METHODS: MG63 was transfected with lentivirus to express CD146 ectopically, and anti-CD146 neutralizing antibody ab75769 was used to inhibit 143B. Cyclic migration of MG63 and co-culture between MG63 and 143B were used to explore the role of OS malignancy in CD146 expression. The effect of OS cell medium (CM) on endothelium behaviors was assessed, and the expression changes of CD146 before and after co-culture of endothelium and OS were evaluated. Finally, the expression of CD146 in OS was detected under different culture conditions, including hyperoxia, low oxygen, high glucose and low glucose conditions. RESULTS: CD146 promoted the colony formation, migration, invasion and homotypic adhesion of OS cells, and reducing the concentration of soluble CD146 in the OS medium inhibited the proliferation, migration and lumen formation of the cultured endothelium. However, CD146 did not affect the adhesion between OS and endothelium, nor did co-culture of both sides affect the CD146 expression. Similarly, the proliferation, migration and CD146 expression of MG63 remained unchanged after many cycles of migration itself, as did its co-culture with 143B for expressing CD146. In addition, we also showed that high glucose promoted the expression of CD146 in OS, while hypoxia had the opposite effect. CONCLUSIONS: These findings demonstrate that CD146 promotes OS progression by mediating pro-tumoral and angiogenic effects. Thus, CD146 could be a potential therapeutic target for OS, especially for OS patients with diabetes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-021-02006-7. BioMed Central 2021-06-08 /pmc/articles/PMC8186124/ /pubmed/34103063 http://dx.doi.org/10.1186/s12935-021-02006-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Primary Research Lei, Xing Wang, Kewei Wang, Wenbo Jin, Hao Gu, Wenguang Chen, Zhiguo Wang, Wei Gao, Kaituo Wang, Huan Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study |
title | Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study |
title_full | Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study |
title_fullStr | Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study |
title_full_unstemmed | Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study |
title_short | Recognize the role of CD146/MCAM in the osteosarcoma progression: an in vitro study |
title_sort | recognize the role of cd146/mcam in the osteosarcoma progression: an in vitro study |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8186124/ https://www.ncbi.nlm.nih.gov/pubmed/34103063 http://dx.doi.org/10.1186/s12935-021-02006-7 |
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