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DEPDC1 as a crucial factor in the progression of human osteosarcoma

Authors :
Lin Shen
Han Li
Ronghan Liu
Chendan Zhou
Morgan Bretches
Xuan Gong
Laitong Lu
Ying Zhang
Kai Zhao
Bin Ning
Shang‐You Yang
Aijun Zhang
Source :
Cancer Medicine, Vol 12, Iss 5, Pp 5798-5808 (2023)
Publication Year :
2023
Publisher :
Wiley, 2023.

Abstract

Abstract 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.

Details

Language :
English
ISSN :
20457634
Volume :
12
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Cancer Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.0e3157066c148909dff996af6b222f5
Document Type :
article
Full Text :
https://doi.org/10.1002/cam4.5340