Diallyl Disulfide Induces Apoptosis and Autophagy in Human Osteosarcoma MG-63 Cells through the PI3K/Akt/mTOR Pathway

Ziqi Yue1, Xin Guan1, Rui Chao1

  • 1Department of Bone Metabolism, School of Stomatology Shandong University, Shandong Provincial Key Laboratory of Oral Tissue Regeneration, Jinan 250012, China.

Insights

Diallyl disulfide (DADs) from garlic inhibits osteosarcoma cell growth by inducing apoptosis and autophagy. This natural compound targets the PI3K/Akt/mTOR pathway, offering potential for new cancer treatments.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Diallyl disulfide (DADs), a natural compound from garlic and scallions, exhibits anti-tumor properties.
  • Osteosarcoma remains a significant challenge in bone cancer treatment.

Purpose of the Study:

  • To investigate the anti-tumor effects of DADs on human osteosarcoma cells (MG-63).
  • To elucidate the underlying mechanisms, including apoptosis, cell cycle arrest, and autophagy, mediated by DADs.

Main Methods:

  • MG-63 cells were treated with varying concentrations of DADs (0-100 μM) for 24-72 hours.
  • Cell viability was assessed using CCK8 assay; apoptosis and cell cycle were analyzed by flow cytometry.
  • Western blot analysis detected key proteins involved in apoptosis (caspase-3, Bax, Bcl-2), autophagy (LC3-II/LC3-I, p62), and the PI3K/Akt/mTOR pathway.

Main Results:

  • DADs significantly inhibited MG-63 cell viability in a dose- and time-dependent manner.
  • DADs induced G2/M cell cycle arrest and increased apoptosis.
  • DADs promoted autophagy, evidenced by increased LC3-II/LC3-I ratio, and inhibited the PI3K/Akt/mTOR pathway, leading to autophagy-mediated cell death.

Conclusions:

  • DADs effectively induces apoptosis and autophagy in human osteosarcoma cells.
  • Inhibition of the PI3K/Akt/mTOR signaling pathway is a key mechanism underlying DADs' anti-tumor effects.
  • DADs presents a promising therapeutic agent for osteosarcoma treatment.

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