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Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma
BACKGROUND: Prognosis of osteosarcoma (OS) with distant metastasis and local recurrence is still poor. Y-box binding protein-1 (YB-1) is a multifunctional protein that can act as a regulator of transcription and translation and its high expression of YB-1 protein was observed in OS, however, the rol...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590655/ https://www.ncbi.nlm.nih.gov/pubmed/23462806 http://dx.doi.org/10.1038/bjc.2012.579 |
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author | Fujiwara-Okada, Y Matsumoto, Y Fukushi, J Setsu, N Matsuura, S Kamura, S Fujiwara, T Iida, K Hatano, M Nabeshima, A Yamada, H Ono, M Oda, Y Iwamoto, Y |
author_facet | Fujiwara-Okada, Y Matsumoto, Y Fukushi, J Setsu, N Matsuura, S Kamura, S Fujiwara, T Iida, K Hatano, M Nabeshima, A Yamada, H Ono, M Oda, Y Iwamoto, Y |
author_sort | Fujiwara-Okada, Y |
collection | PubMed |
description | BACKGROUND: Prognosis of osteosarcoma (OS) with distant metastasis and local recurrence is still poor. Y-box binding protein-1 (YB-1) is a multifunctional protein that can act as a regulator of transcription and translation and its high expression of YB-1 protein was observed in OS, however, the role of YB-1 in OS remains unclear. METHODS: Y-box binding protein-1 expression in OS cells was inhibited by specific small interfering RNAs to YB-1 (si-YB-1). The effects of si-YB-1 in cell proliferation and cell cycle transition in OS cells were analysed in vitro and in vivo. The association of nuclear expression of YB-1 and clinical prognosis was also investigated by immunohistochemistry. RESULTS: Proliferation of OS cell was suppressed by si-YB-1 in vivo and in vitro. The expression of cyclin D1 and cyclin A were also decreased by si-YB-1. In addition, si-YB-1 induced G1/S arrest with decreased cyclin D1 and cyclin A in OS cell lines. Direct binding of YB-1 in OS cell lines was also observed. Finally, the nuclear expression of YB-1 was significantly related to the poorer overall survival in OS patients. CONCLUSION: Y-box binding protein-1 would regulate cell cycle progression at G1/S and tumour growth in human OS cells in vitro and in vivo. Nuclear expression of YB-1 was closely associated with the prognosis of OS, thus, YB-1 simultaneously could be a potent molecular target and prognostic biomarker for OS. |
format | Online Article Text |
id | pubmed-3590655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-35906552014-03-05 Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma Fujiwara-Okada, Y Matsumoto, Y Fukushi, J Setsu, N Matsuura, S Kamura, S Fujiwara, T Iida, K Hatano, M Nabeshima, A Yamada, H Ono, M Oda, Y Iwamoto, Y Br J Cancer Translational Therapeutics BACKGROUND: Prognosis of osteosarcoma (OS) with distant metastasis and local recurrence is still poor. Y-box binding protein-1 (YB-1) is a multifunctional protein that can act as a regulator of transcription and translation and its high expression of YB-1 protein was observed in OS, however, the role of YB-1 in OS remains unclear. METHODS: Y-box binding protein-1 expression in OS cells was inhibited by specific small interfering RNAs to YB-1 (si-YB-1). The effects of si-YB-1 in cell proliferation and cell cycle transition in OS cells were analysed in vitro and in vivo. The association of nuclear expression of YB-1 and clinical prognosis was also investigated by immunohistochemistry. RESULTS: Proliferation of OS cell was suppressed by si-YB-1 in vivo and in vitro. The expression of cyclin D1 and cyclin A were also decreased by si-YB-1. In addition, si-YB-1 induced G1/S arrest with decreased cyclin D1 and cyclin A in OS cell lines. Direct binding of YB-1 in OS cell lines was also observed. Finally, the nuclear expression of YB-1 was significantly related to the poorer overall survival in OS patients. CONCLUSION: Y-box binding protein-1 would regulate cell cycle progression at G1/S and tumour growth in human OS cells in vitro and in vivo. Nuclear expression of YB-1 was closely associated with the prognosis of OS, thus, YB-1 simultaneously could be a potent molecular target and prognostic biomarker for OS. Nature Publishing Group 2013-03-05 2013-03-05 /pmc/articles/PMC3590655/ /pubmed/23462806 http://dx.doi.org/10.1038/bjc.2012.579 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Translational Therapeutics Fujiwara-Okada, Y Matsumoto, Y Fukushi, J Setsu, N Matsuura, S Kamura, S Fujiwara, T Iida, K Hatano, M Nabeshima, A Yamada, H Ono, M Oda, Y Iwamoto, Y Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
title | Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
title_full | Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
title_fullStr | Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
title_full_unstemmed | Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
title_short | Y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
title_sort | y-box binding protein-1 regulates cell proliferation and is associated with clinical outcomes of osteosarcoma |
topic | Translational Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590655/ https://www.ncbi.nlm.nih.gov/pubmed/23462806 http://dx.doi.org/10.1038/bjc.2012.579 |
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