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DEPDC1 as a crucial factor in the progression of human osteosarcoma
OBJECTIVE: Novel therapeutic strategies are emerging with the increased understanding of the underlying mechanisms of human osteosarcoma. This current study tends to decipher the potentially critical role of DEP domain‐containing 1 (DEPDC1), a tumor‐related gene, during the progression of osteosarco...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028160/ https://www.ncbi.nlm.nih.gov/pubmed/36479633 http://dx.doi.org/10.1002/cam4.5340 |
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author | Shen, Lin Li, Han Liu, Ronghan Zhou, Chendan Bretches, Morgan Gong, Xuan Lu, Laitong Zhang, Ying Zhao, Kai Ning, Bin Yang, Shang‐You Zhang, Aijun |
author_facet | Shen, Lin Li, Han Liu, Ronghan Zhou, Chendan Bretches, Morgan Gong, Xuan Lu, Laitong Zhang, Ying Zhao, Kai Ning, Bin Yang, Shang‐You Zhang, Aijun |
author_sort | Shen, Lin |
collection | PubMed |
description | OBJECTIVE: Novel therapeutic strategies are emerging with the increased understanding of the underlying mechanisms of human osteosarcoma. This current study tends to decipher the potentially critical role of DEP domain‐containing 1 (DEPDC1), a tumor‐related gene, during the progression of osteosarcoma. METHODS: Bioinformatics analysis of 25,035 genes from the National Center for Biotechnology Information (NCBI) databases was performed to screen differentially expressed genes between osteosarcoma and normal control groups, complemented by the examination of 85 clinical osteosarcoma specimens. Furthermore, the manipulation of DEPDC1 expression levels by using silencing RNA (siRNA) or lentiviral vector intervention on human osteosarcoma cells was performed to reveal its role and interactions in in vitro and in vivo settings. RESULTS: Gene expression profile analysis and immunohistochemical (IHC) examination suggested that DEPDC1 is highly expressed in human osteosarcoma cells and tumor tissue. The silencing of DEPDC1 arrested osteosarcoma cell proliferation, promoted apoptosis, and ceased tumor metastasis. Studies involving clinical human osteosarcoma cases exhibited a strong correlation of DEPDC1 over‐expressed osteosarcoma specimens with a reduced patient survival rate. CONCLUSIONS: Collectively, this study demonstrated that DEPDC1 is a critical driver in the promotion of osteosarcoma progression and results in poor patient prognosis. Genetically targeting or pharmacologically inhibiting DEPDC1 may serve as a promising strategy for treating human osteosarcoma. |
format | Online Article Text |
id | pubmed-10028160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100281602023-03-22 DEPDC1 as a crucial factor in the progression of human osteosarcoma Shen, Lin Li, Han Liu, Ronghan Zhou, Chendan Bretches, Morgan Gong, Xuan Lu, Laitong Zhang, Ying Zhao, Kai Ning, Bin Yang, Shang‐You Zhang, Aijun Cancer Med RESEARCH ARTICLES OBJECTIVE: Novel therapeutic strategies are emerging with the increased understanding of the underlying mechanisms of human osteosarcoma. This current study tends to decipher the potentially critical role of DEP domain‐containing 1 (DEPDC1), a tumor‐related gene, during the progression of osteosarcoma. METHODS: Bioinformatics analysis of 25,035 genes from the National Center for Biotechnology Information (NCBI) databases was performed to screen differentially expressed genes between osteosarcoma and normal control groups, complemented by the examination of 85 clinical osteosarcoma specimens. Furthermore, the manipulation of DEPDC1 expression levels by using silencing RNA (siRNA) or lentiviral vector intervention on human osteosarcoma cells was performed to reveal its role and interactions in in vitro and in vivo settings. RESULTS: Gene expression profile analysis and immunohistochemical (IHC) examination suggested that DEPDC1 is highly expressed in human osteosarcoma cells and tumor tissue. The silencing of DEPDC1 arrested osteosarcoma cell proliferation, promoted apoptosis, and ceased tumor metastasis. Studies involving clinical human osteosarcoma cases exhibited a strong correlation of DEPDC1 over‐expressed osteosarcoma specimens with a reduced patient survival rate. CONCLUSIONS: Collectively, this study demonstrated that DEPDC1 is a critical driver in the promotion of osteosarcoma progression and results in poor patient prognosis. Genetically targeting or pharmacologically inhibiting DEPDC1 may serve as a promising strategy for treating human osteosarcoma. John Wiley and Sons Inc. 2022-12-07 /pmc/articles/PMC10028160/ /pubmed/36479633 http://dx.doi.org/10.1002/cam4.5340 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Shen, Lin Li, Han Liu, Ronghan Zhou, Chendan Bretches, Morgan Gong, Xuan Lu, Laitong Zhang, Ying Zhao, Kai Ning, Bin Yang, Shang‐You Zhang, Aijun DEPDC1 as a crucial factor in the progression of human osteosarcoma |
title |
DEPDC1 as a crucial factor in the progression of human osteosarcoma |
title_full |
DEPDC1 as a crucial factor in the progression of human osteosarcoma |
title_fullStr |
DEPDC1 as a crucial factor in the progression of human osteosarcoma |
title_full_unstemmed |
DEPDC1 as a crucial factor in the progression of human osteosarcoma |
title_short |
DEPDC1 as a crucial factor in the progression of human osteosarcoma |
title_sort | depdc1 as a crucial factor in the progression of human osteosarcoma |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028160/ https://www.ncbi.nlm.nih.gov/pubmed/36479633 http://dx.doi.org/10.1002/cam4.5340 |
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