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Updated: Jan 6, 2026

Three-Dimensional Bone Extracellular Matrix Model for Osteosarcoma
Published on: April 12, 2019
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.
Abstract:
Background: Despite the characters of the resistance of tumour of ailanthone (AIL) were found in various tumour cells, its effect on osteosarcoma is still unclear. Herein, we attempted to see the effects of AIL on an osteosarcoma cell line MG63. Methods: MG63 cells were treated by AIL, following which CCK-8 assay, BrdU assay, Transwell assay and Western blot were utilized to detect cell proliferation, migration, invasion and apoptosis. miR-126 expression in osteosarcoma tissues and cell lines was measured by qRT-PCR. Further, the target of miR-126 and the downstream signalling for AIL were studied. Results: Treating MG63 cells with 1.5 μM AIL for 24 h significantly suppressed proliferation, migration, invasion and induced apoptosis. Meanwhile, AIL inhibited PI3K/AKT pathway and up-regulated miR-126 expression. miR-126 of osteosarcoma tissues and cell lines was low expressed, as relative to paracancerous tissues and normal osteoblast. The anti-tumour effects of AIL were attenuated by miR-126 silencing. Further, VEGF-A was a target of miR-126. Conclusions: This study demonstrated that AIL was effective in inhibiting MG63 cells growth, migration and invasion. The anti-tumour properties may be via up-regulating miR-126 and thereby degradation of VEGF-A.
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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