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Updated: Apr 16, 2026

Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
Published on: October 4, 2019
Survivin small interfering RNA suppresses glioblastoma growth by inducing cellular apoptosis
Yanbo Liu1, Chunming Miao1, Zhenjiang Wang1
1Beihua University Faculty of Medicine, Jilin 132013, Jilin Province, China.
Abstract:
A survivin small interfering RNA sequence specific for a human and mouse homogenous sequence was constructed. Survivin small interfering RNA could significantly inhibit glioma cell proliferation and induce apoptosis when it was transfected into either a human glioma cell line U251 or rat glioma C6 cells in vitro. In addition, treatment of rat orthotopic glioma models with survivin small interfering demonstrated the inhibition of glioma growth in vivo. Our experimental findings suggest that the use of RNA interference techniques to target the survivin sequence may be useful in the treatment of glioma.
Insights
Small interfering RNA targeting survivin effectively inhibited glioma cell growth and promoted apoptosis in vitro and in vivo. This suggests RNA interference targeting survivin may be a promising glioma treatment strategy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Glioblastoma is an aggressive brain tumor with limited treatment options.
- Survivin is a protein that promotes cancer cell survival and proliferation.
- Targeting survivin offers a potential therapeutic strategy for glioblastoma.
Purpose of the Study:
- To investigate the efficacy of survivin small interfering RNA (siRNA) in inhibiting glioma growth.
- To evaluate the potential of RNA interference (RNAi) as a treatment for glioma.
Main Methods:
- Constructed a survivin-specific small interfering RNA (siRNA) targeting a conserved human and mouse sequence.
- Transfected siRNA into human U251 and rat C6 glioma cell lines in vitro.
- Administered siRNA to rat orthotopic glioma models in vivo.
Main Results:
- Survivin siRNA significantly inhibited glioma cell proliferation in both human and rat cell lines.
- Survivin siRNA induced apoptosis in glioma cells in vitro.
- Treatment with survivin siRNA demonstrated inhibition of glioma tumor growth in vivo.
Conclusions:
- Survivin siRNA effectively suppresses glioma cell proliferation and induces apoptosis.
- RNA interference targeting survivin shows potential as a therapeutic approach for glioma treatment.
- Further research into survivin-targeted RNAi is warranted for clinical application in glioma therapy.
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