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Updated: Apr 25, 2026

Colony Formation Assay Detecting the Proliferative Capacity of LncRNA-knockdown Osteosarcoma Cells
Published on: January 16, 2026
Knockdown of Aurora-B inhibits osteosarcoma cell invasion and migration via modulating PI3K/Akt/NF-κB signaling
Liang Bo Zhu1, Jian Jiang2, Xiao Ping Zhu3
1Department of Orthopedics, The First Affiliated Hospital of Nanchang University Jiangxi, China.
Abstract:
Increasing evidences reveal that Aurora-B may be involved in metastasis of malignant tumor. In this study, we investigated the inhibitory effect of Aurora-B on invasion and migration of OS cells and the activity of PI3K/Akt/NF-κB signaling pathway in vitro. The expression of Aurora-B and p-Akt (Ser473) proteins was detected by immunohistochemistry in OS tissues from 24 patients with pulmonary metastatic disease, and the relationship between Aurora-B and p-Akt was investigated. The results showed that there was a positive correlation between Aurora-B and p-Akt protein expression. Furthermore, we down-regulated the expression of Aurora-B through a recombinant lentivirus (Lv-shAURKB). Migration and invasion of cells were investigated by wound healing and transwell invasion assays. Results showed that silencing Aurora-B inhibited cell migratory and invasive ability of OS cells in vitro. Finally, knockdown of Aurora-B suppresses the activity of PI3K/Akt/NF-κB signaling pathway in OS cells. Our results indicated that knockdown of Aurora-B suppresses OS cells migratory and invasive ability via modulating the "PI3K/Akt/NF-κB" signaling pathway in vitro. The Aurora-B blocker may be a new therapeutic strategy in OS management.
Insights
Aurora-B inhibition significantly reduces osteosarcoma (OS) cell migration and invasion by suppressing the PI3K/Akt/NF-κB pathway. This suggests Aurora-B blockers could be a novel therapeutic strategy for managing OS metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Metastasis is a critical factor in malignant tumor progression.
- Aurora-B kinase has been implicated in the metastasis of various cancers.
- The role of Aurora-B in osteosarcoma (OS) metastasis requires further elucidation.
Purpose of the Study:
- To investigate the inhibitory effect of Aurora-B on OS cell invasion and migration.
- To explore the impact of Aurora-B on the PI3K/Akt/NF-κB signaling pathway.
- To assess the correlation between Aurora-B and p-Akt expression in OS tissues.
Main Methods:
- Immunohistochemistry to detect Aurora-B and p-Akt (Ser473) protein expression in patient tissues.
- Recombinant lentivirus (Lv-shAURKB) for Aurora-B gene silencing.
- In vitro assays including wound healing and Transwell invasion assays.
- Western blot analysis to assess PI3K/Akt/NF-κB pathway activity.
Main Results:
- A positive correlation was observed between Aurora-B and p-Akt protein expression in OS tissues.
- Silencing Aurora-B significantly inhibited OS cell migration and invasion in vitro.
- Knockdown of Aurora-B suppressed the activity of the PI3K/Akt/NF-κB signaling pathway.
Conclusions:
- Aurora-B plays a crucial role in promoting OS cell migration and invasion.
- Down-regulation of Aurora-B suppresses OS cell metastasis by modulating the PI3K/Akt/NF-κB pathway.
- Targeting Aurora-B represents a potential therapeutic strategy for osteosarcoma management.
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