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Updated: Aug 22, 2026

Identification of Intracellular Signaling Events Induced in Viable Cells by Interaction with Neighboring Cells Undergoing Apoptotic Cell Death
Published on: December 27, 2016
[Effect of melittin on apoptosis and necrosis of U2 OS cells]
Yong-Qiang Chen1, Zhen-An Zhu, Yong-Qiang Hao
1Department of Orthopaedics, Shanghai Ninth People's Hospital, Shanghai Second Medical University, Shanghai 200011, China. YQCHEN116@hotmail.com
Objective:
To study the effect of melittin on apoptsis and necrosis of osteosarcoma cell line U2 OS in vitro.
Methods:
Osteosarcoma cell line U2 OS was treated with melittin. The growth and proliferation was observed by MTT assay and cell counting, and the necrosis was estimated by Trypan blue staining. The cell apoptsis, Fas and Apo2. 7 expression were detected by cytometer.
Results:
The data showed that melittin could inhibit the proliferation of U2 OS dose-dependently at 16 and 64 mg/L. Cell apoptsis was detected by cytometer, when the cells were treated by 16 mg/L and 32 mg/L of melittin respectively, and the percentages of Fas and Apo2. 7 positive cells were increased.
Conclusion:
Melittin inhibits the proliferation of osterosarcoma cell line through up-regulating Fas expression and inducing apoptsis.
Insights
Melittin effectively inhibits osteosarcoma cell proliferation and induces apoptosis in vitro. This bee venom component up-regulates Fas expression, offering potential therapeutic insights for bone cancer treatment.
Area of Science:
- Biochemistry
- Cell Biology
- Oncology
Background:
- Osteosarcoma is a primary bone malignancy with limited treatment options.
- Melittin, a peptide from bee venom, exhibits diverse biological activities.
Purpose of the Study:
- To investigate the in vitro effects of melittin on osteosarcoma cell line U2 OS.
- To determine melittin's impact on apoptosis and necrosis in U2 OS cells.
Main Methods:
- U2 OS cells were treated with varying concentrations of melittin.
- Cell proliferation assessed via MTT assay and cell counting.
- Necrosis evaluated using Trypan blue staining.
- Apoptosis, Fas, and Apo2.7 expression analyzed by flow cytometry.
Main Results:
- Melittin demonstrated dose-dependent inhibition of U2 OS cell proliferation at 16 and 64 mg/L.
- Treatment with melittin (16 and 32 mg/L) significantly increased apoptosis.
- Fas and Apo2.7 positive cell percentages were elevated following melittin treatment.
Conclusions:
- Melittin inhibits osteosarcoma cell proliferation.
- Melittin induces apoptosis in osteosarcoma cells.
- Upregulation of Fas expression is a key mechanism by which melittin exerts its anti-cancer effects.
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