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.

Journal of Bone Oncology
|January 24, 2025
PubMed
Abstract

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.

Related Concept Videos

mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
3.7K
Mitogens and the Cell Cycle02:38

Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...
6.4K
PI3K/mTOR/AKT Signaling Pathway01:22

PI3K/mTOR/AKT Signaling Pathway

The mammalian target of rapamycin  (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1  (mTORC1) and mTOR complex 2  (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast,  mTORC2 consists of a...
3.4K