The anti-osteosarcoma property of ailanthone through regulation of miR-126/VEGF-A axis

Daliang Kong1, Boda Ying2, Jinrui Zhang1

  • 1Department of Orthopaedics, China-Japan Union Hospital of Jilin University , Changchun , China.

Insights

Ailanthone (AIL) effectively inhibited osteosarcoma cell growth, migration, and invasion. This anti-tumor effect is linked to increased miR-126 and decreased VEGF-A, offering potential therapeutic strategies.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Ailanthone (AIL) shows anti-tumor properties in various cells, but its effect on osteosarcoma remains unknown.
  • Osteosarcoma is a primary bone malignancy with significant unmet therapeutic needs.

Purpose of the Study:

  • To investigate the anti-cancer effects of AIL on the MG63 osteosarcoma cell line.
  • To elucidate the molecular mechanisms underlying AIL's action, focusing on miR-126 and the PI3K/AKT pathway.

Main Methods:

  • Cell proliferation, migration, and invasion assays (CCK-8, BrdU, Transwell) were performed on AIL-treated MG63 cells.
  • Western blot and qRT-PCR were used to analyze protein expression, apoptosis, and miR-126 levels.
  • The regulatory relationship between miR-126 and VEGF-A was investigated.

Main Results:

  • AIL treatment significantly suppressed MG63 cell proliferation, migration, and invasion while inducing apoptosis.
  • AIL upregulated miR-126 expression and inhibited the PI3K/AKT signaling pathway.
  • Osteosarcoma tissues and cell lines exhibited low miR-126 expression; miR-126 silencing attenuated AIL's anti-tumor effects.
  • VEGF-A was identified as a direct target of miR-126.

Conclusions:

  • Ailanthone demonstrates significant anti-proliferative, anti-migratory, and anti-invasive effects on osteosarcoma cells.
  • The anti-tumor activity of AIL is mediated through the upregulation of miR-126, leading to the degradation of VEGF-A.

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