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Updated: May 31, 2025

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
Using β-Elemene to reduce stemness and drug resistance in osteosarcoma: A focus on the AKT/FOXO1 signaling pathway
Shaochun Zhang1, Zhijie Xing1, Jing Ke2
1Orthopedics Department, The Central Hospital of Ezhou, Ezhou 436000, China.
Objective:
Osteosarcoma, a highly malignant bone tumor, poses significant treatment challenges due to its propensity for stemness and drug resistance, particularly against doxorubicin (DOX). This study aims to investigate the mechanism by which β-elemene reduces the stemness of osteosarcoma stem cells and ultimately decreases DOX resistance by inhibiting the Akt/FoxO1 signaling pathway and activating a macrophage-mediated inflammatory microenvironment.
Methods:
Osteosarcoma stem cells were isolated and induced for DOX resistance. In vitro and in vivo models were employed to assess β-elemene's impact on cell viability, stemness, and drug resistance. Bioinformatics analysis, flow cytometry, and immunofluorescence staining were used to evaluate signaling pathway activity and macrophage polarization. Additionally, an osteosarcoma xenograft mouse model was established to confirm the therapeutic effects of β-elemene.
Results:
In vivo animal experiments demonstrated that β-elemene reduces osteosarcoma resistance. Bioinformatics analysis revealed that AKT1 is a key core gene in osteosarcoma progression, acting through the FOXO signaling pathway. Additionally, AKT inhibits immune cell infiltration in osteosarcoma and suppresses immune responses during osteosarcoma progression. β-elemene may influence osteosarcoma progression by mediating TP53 to regulate PTEN and subsequently AKT1. In vitro experiments showed that β-elemene promotes M1 macrophage activation by inhibiting the Akt/FoxO1 signaling axis, thereby reducing the stemness of osteosarcoma stem cells. Finally, in vivo animal experiments confirmed that β-elemene reduces osteosarcoma resistance by promoting M1 macrophage activation through inhibition of the Akt/FoxO1 signaling axis.
Conclusion:
β-Elemene demonstrates promising potential in reducing osteosarcoma stemness and drug resistance via dual mechanisms: targeting the AKT/FOXO1 pathway and modulating the tumor immune microenvironment. These findings suggest β-elemene as a potential adjunct therapy for osteosarcoma, providing novel therapeutic strategies to overcome chemotherapy resistance and improve patient outcomes.
Insights
Beta-elemene combats osteosarcoma stemness and doxorubicin resistance by inhibiting the Akt/FoxO1 pathway and activating anti-tumor M1 macrophages. This dual action offers a promising strategy for improving osteosarcoma treatment outcomes.
Area of Science:
- Oncology
- Pharmacology
- Immunology
Background:
- Osteosarcoma is a malignant bone tumor with significant treatment challenges, including stemness and drug resistance, particularly to doxorubicin (DOX).
- Understanding the mechanisms underlying osteosarcoma stemness and drug resistance is crucial for developing effective therapeutic strategies.
Purpose of the Study:
- To investigate how beta-elemene reduces osteosarcoma stemness and doxorubicin resistance.
- To elucidate the role of the Akt/FoxO1 signaling pathway and macrophage activation in beta-elemene's therapeutic effects.
Main Methods:
- Utilized in vitro and in vivo osteosarcoma models, including drug-resistant stem cells and xenograft mouse models.
- Employed bioinformatics analysis, flow cytometry, and immunofluorescence staining to assess signaling pathways and macrophage polarization.
- Evaluated beta-elemene's impact on cell viability, stemness, drug resistance, and immune cell infiltration.
Main Results:
- Beta-elemene demonstrated efficacy in reducing osteosarcoma resistance in vivo.
- Inhibition of the Akt/FoxO1 signaling pathway by beta-elemene was observed, potentially mediated by TP53 regulating PTEN and AKT1.
- Beta-elemene promoted M1 macrophage activation, which in turn reduced osteosarcoma stemness and drug resistance.
Conclusions:
- Beta-elemene exhibits potential in reducing osteosarcoma stemness and drug resistance through dual mechanisms.
- Targeting the Akt/FoxO1 pathway and modulating the tumor immune microenvironment are key actions of beta-elemene.
- Beta-elemene may serve as an effective adjunct therapy for osteosarcoma, offering new strategies to overcome chemotherapy resistance.
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