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B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma
BACKGROUND: Lung adenocarcinoma is the most common pathological type of lung cancer. However, the mechanisms underlying its development are still poorly understood. B7-H3 was discovered as a new member of the B7 costimulatory family. METHODS: We detected the expression status of B7-H3 protein in lun...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091475/ https://www.ncbi.nlm.nih.gov/pubmed/30127617 http://dx.doi.org/10.2147/OTT.S169811 |
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author | Yu, Ting-Ting Zhang, Tao Lu, Xi Wang, Ruo-Zheng |
author_facet | Yu, Ting-Ting Zhang, Tao Lu, Xi Wang, Ruo-Zheng |
author_sort | Yu, Ting-Ting |
collection | PubMed |
description | BACKGROUND: Lung adenocarcinoma is the most common pathological type of lung cancer. However, the mechanisms underlying its development are still poorly understood. B7-H3 was discovered as a new member of the B7 costimulatory family. METHODS: We detected the expression status of B7-H3 protein in lung adenocarcinoma tissues, and evaluated the relationship of B7-H3 expression and patients’ prognosis. Then, we silenced its expression in A549 cells by transient siRNA transfection to ascertain the function of B7-H3 in lung adenocarcinoma cells. Western blotting was used to detect the expression of epithelial–mesenchymal transition (EMT) related proteins. RESULTS: We found that B7-H3 overexpressed in lung adenocarcinoma. It is correlated with lymph node metastasis, distant metastasis, and disease stage. The Cox regression analysis showed that B7-H3 might serve as an independent prognostic marker of lung adenocarcinoma. We also found that B7-H3 promoted proliferation, invasion and migration of A549 cells in vitro. B7-H3 also could promote EMT progression by regulating EMT-related molecules. CONCLUSION: B7-H3 is a potential target for the treatment of lung adenocarcinoma. |
format | Online Article Text |
id | pubmed-6091475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60914752018-08-20 B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma Yu, Ting-Ting Zhang, Tao Lu, Xi Wang, Ruo-Zheng Onco Targets Ther Original Research BACKGROUND: Lung adenocarcinoma is the most common pathological type of lung cancer. However, the mechanisms underlying its development are still poorly understood. B7-H3 was discovered as a new member of the B7 costimulatory family. METHODS: We detected the expression status of B7-H3 protein in lung adenocarcinoma tissues, and evaluated the relationship of B7-H3 expression and patients’ prognosis. Then, we silenced its expression in A549 cells by transient siRNA transfection to ascertain the function of B7-H3 in lung adenocarcinoma cells. Western blotting was used to detect the expression of epithelial–mesenchymal transition (EMT) related proteins. RESULTS: We found that B7-H3 overexpressed in lung adenocarcinoma. It is correlated with lymph node metastasis, distant metastasis, and disease stage. The Cox regression analysis showed that B7-H3 might serve as an independent prognostic marker of lung adenocarcinoma. We also found that B7-H3 promoted proliferation, invasion and migration of A549 cells in vitro. B7-H3 also could promote EMT progression by regulating EMT-related molecules. CONCLUSION: B7-H3 is a potential target for the treatment of lung adenocarcinoma. Dove Medical Press 2018-08-10 /pmc/articles/PMC6091475/ /pubmed/30127617 http://dx.doi.org/10.2147/OTT.S169811 Text en © 2018 Yu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Yu, Ting-Ting Zhang, Tao Lu, Xi Wang, Ruo-Zheng B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
title | B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
title_full | B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
title_fullStr | B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
title_full_unstemmed | B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
title_short | B7-H3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
title_sort | b7-h3 promotes metastasis, proliferation, and epithelial-mesenchymal transition in lung adenocarcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6091475/ https://www.ncbi.nlm.nih.gov/pubmed/30127617 http://dx.doi.org/10.2147/OTT.S169811 |
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