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AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression
Background: AEG-1 has been proven to be tumor enhancer in gastric cancer. However, its mechanism has not yet been fully clarified. Methods: Gain-of-function and loss-of-function experiments were conducted to determine the role of eIF4E in AEG-1-induced growth of gastric cancer cells and xenografts o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659790/ https://www.ncbi.nlm.nih.gov/pubmed/31413586 http://dx.doi.org/10.2147/OTT.S213604 |
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author | Wu, Shengjie Zhang, Zuhao Wu, Dandan Chen, Hongling Qian, Xixi Wang, Xuerong Huang, Wenbin |
author_facet | Wu, Shengjie Zhang, Zuhao Wu, Dandan Chen, Hongling Qian, Xixi Wang, Xuerong Huang, Wenbin |
author_sort | Wu, Shengjie |
collection | PubMed |
description | Background: AEG-1 has been proven to be tumor enhancer in gastric cancer. However, its mechanism has not yet been fully clarified. Methods: Gain-of-function and loss-of-function experiments were conducted to determine the role of eIF4E in AEG-1-induced growth of gastric cancer cells and xenografts of a nude mouse model. Western blot analysis and SRB assay were used to determine the protein expression levels and survival cell numbers. Results: Silencing the expression of AEG-1 inhibited the growth of gastric cancer cells in parallel with a decreased eIF4E and cyclin D1 expression; however, the overexpression of AEG-1 promoted cell growth and increased eIF4E and cyclin D1 expression. Moreover, the overexpression of eIF4E partially reversed the AEG-1 silencing-induced reduction of cyclin D1 and the inhibition of cell growth. An eIF4E knockdown also partially reversed the AEG-1 overexpression-induced upregulation of cyclin D1 and cell growth. Notably, manipulating the expression of eIF4E did not affect the expression of AEG-1. Finally, the silencing of AEG-1 expression inhibited the growth of SGC-7901 xenografts in parallel with the downregulation of eIF4E and cyclin D1 expression in the nude mouse model. Conclusion: AEG-1 promoted the growth of gastric cancer through upregulation of eIF4E/cyclin D1 signaling pathway. |
format | Online Article Text |
id | pubmed-6659790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-66597902019-08-14 AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression Wu, Shengjie Zhang, Zuhao Wu, Dandan Chen, Hongling Qian, Xixi Wang, Xuerong Huang, Wenbin Onco Targets Ther Original Research Background: AEG-1 has been proven to be tumor enhancer in gastric cancer. However, its mechanism has not yet been fully clarified. Methods: Gain-of-function and loss-of-function experiments were conducted to determine the role of eIF4E in AEG-1-induced growth of gastric cancer cells and xenografts of a nude mouse model. Western blot analysis and SRB assay were used to determine the protein expression levels and survival cell numbers. Results: Silencing the expression of AEG-1 inhibited the growth of gastric cancer cells in parallel with a decreased eIF4E and cyclin D1 expression; however, the overexpression of AEG-1 promoted cell growth and increased eIF4E and cyclin D1 expression. Moreover, the overexpression of eIF4E partially reversed the AEG-1 silencing-induced reduction of cyclin D1 and the inhibition of cell growth. An eIF4E knockdown also partially reversed the AEG-1 overexpression-induced upregulation of cyclin D1 and cell growth. Notably, manipulating the expression of eIF4E did not affect the expression of AEG-1. Finally, the silencing of AEG-1 expression inhibited the growth of SGC-7901 xenografts in parallel with the downregulation of eIF4E and cyclin D1 expression in the nude mouse model. Conclusion: AEG-1 promoted the growth of gastric cancer through upregulation of eIF4E/cyclin D1 signaling pathway. Dove 2019-07-22 /pmc/articles/PMC6659790/ /pubmed/31413586 http://dx.doi.org/10.2147/OTT.S213604 Text en © 2019 Wu et al. http://creativecommons.org/licenses/by-nc/3.0/ 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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Wu, Shengjie Zhang, Zuhao Wu, Dandan Chen, Hongling Qian, Xixi Wang, Xuerong Huang, Wenbin AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression |
title | AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression |
title_full | AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression |
title_fullStr | AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression |
title_full_unstemmed | AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression |
title_short | AEG-1 promotes the growth of gastric cancer through the upregulation of eIF4E expression |
title_sort | aeg-1 promotes the growth of gastric cancer through the upregulation of eif4e expression |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659790/ https://www.ncbi.nlm.nih.gov/pubmed/31413586 http://dx.doi.org/10.2147/OTT.S213604 |
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