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β-Aescin shows potent antiproliferative activity in osteosarcoma cells by inducing autophagy, ROS generation and
Zhao-Rui Liu1, Li-Zhi Sun, Tang-Hong Jia
1Department of Orthopaedic Surgery, Jinan Central Hospital, Jinan 250013, Shandong, China.
Purpose:
Osteosarcoma is one of the frequent bone tumor affecting mainly children and is associated with considerable mortality. The limited availability of anticancer drugs and less efficacious treatment options have led to poor survival rates of patients with osteosarcoma. Therefore, there is need to look for more viable treatment options and against this backdrop, natural products may prove handy. Therefore the aim of the present study was to evaluate the anticancer activity of a natural product of plant origin, β-aescin, against U2OS human osteosarcoma cells.
Methods:
U205 human osteosarcoma cell line was used in this study. Antiproliferative activity was determined by MTT assay. Reactive oxygen species (ROS) and mitochondrial membrane potential (MMP) were evaluated by flow cytometry. Autophagy was detected by monodansylcadaverine (MDC) staining and immunofluorescence. Protein expression was examined by western blotting.
Results:
The results indicated that β-aescin showed significant anticancer activity against U2OS human osteosarcoma cells and exhibited an IC50 of 40 μM. β-aescin treatment caused significant increase in ROS and decrease in the MMP. The anticancer effect of β-aescin was found to be due mainly to autophagic cell death as evidenced from MDC staining and immunofluorescence. Moreover, β-aescin caused significant increase in the expression levels of LC3- II protein in U2OS osteosarcoma cells in a time and dosedependent manner.
Conclusion:
Taken together we propose that β-aescin may prove a lead molecule in the management of osteosarcoma and deserves further research efforts.
Insights
Beta-aescin, a natural product, demonstrates significant anticancer activity against osteosarcoma cells by inducing cell death through autophagy. This plant-derived compound shows promise as a potential therapeutic agent for osteosarcoma management.
Area of Science:
- Oncology
- Natural Product Chemistry
- Cell Biology
Background:
- Osteosarcoma is a prevalent bone tumor in children with high mortality.
- Limited treatment options and drug efficacy contribute to poor patient survival rates.
- Natural products offer potential alternative therapeutic strategies for osteosarcoma.
Purpose of the Study:
- To evaluate the anticancer potential of beta-aescin, a plant-derived natural product.
- To investigate the effects of beta-aescin on U2OS human osteosarcoma cells.
- To explore the mechanisms underlying beta-aescin's anti-cancer activity.
Main Methods:
- Utilized U2OS human osteosarcoma cell line.
- Assessed antiproliferative activity via MTT assay.
- Quantified reactive oxygen species (ROS) and mitochondrial membrane potential (MMP) using flow cytometry.
- Detected autophagy using monodansylcadaverine (MDC) staining and immunofluorescence.
- Examined protein expression, specifically LC3-II, through western blotting.
Main Results:
- Beta-aescin exhibited significant anticancer activity with an IC50 of 40 μM against U2OS cells.
- Treatment with beta-aescin led to increased ROS levels and decreased MMP.
- Autophagic cell death was identified as the primary mechanism of beta-aescin's anticancer effect.
- Beta-aescin dose-dependently increased the expression of LC3-II protein, a marker of autophagy.
Conclusions:
- Beta-aescin demonstrates potent anticancer effects against osteosarcoma cells.
- The anti-cancer activity is mediated through the induction of autophagic cell death.
- Beta-aescin warrants further investigation as a potential lead compound for osteosarcoma treatment.
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