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Updated: May 24, 2026

Murine Model for Non-invasive Imaging to Detect and Monitor Ovarian Cancer Recurrence
Published on: November 2, 2014
Effect of shRNA targeting survivin on ovarian cancer
Jun Xing1, Chang-Ru Jia, Yan Wang
1Department of Gastrointestinal Surgery, The Third Hospital of Harbin Medical University, No. 150, Ha Ping Road, Nan Gang District, Heilongjiang Province, People's Republic of China.
Purpose:
This study investigated the effect of shRNA targeting survivin on cultured ovarian cancer cells and on a murine ovarian cancer xenograft.
Methods:
An RNAi plasmid for survivin was transfected into SKOV3 cells, and the effect of shRNA targeting survivin on the expression of survivin was determined. Transmission electron microscopy (TEM), flow cytometry, and TUNEL staining were used to assess apoptosis. The MTT assay was used to measure cell growth and changes in cisplatin sensitivity. SKOV3 cells were injected into nude mice, and the effect of shRNA targeting the survivin gene on tumor growth was assessed.
Results:
SKOV3 cells transfected with an RNAi plasmid against survivin had increased apoptosis and slower growth. At the molecular level, these cells also had lower expression of survivin. Nude mice inoculated with SKOV3 cells developed cancers, and treatment with shRNA targeting survivin markedly inhibited the growth of these cancers with no obvious side effects.
Conclusions:
Our studies of SKOV3 cells and ovarian cancer xenografts in nude mice indicate that shRNA targeting survivin has potential for the treatment of ovarian cancer.
Insights
Short hairpin RNA (shRNA) targeting survivin effectively reduced ovarian cancer cell growth and survivin expression in cell cultures and xenografts. This suggests shRNA targeting survivin is a promising therapeutic strategy for ovarian cancer.
Area of Science:
- Oncology
- Molecular Biology
- Gene Therapy
Background:
- Survivin is a key protein involved in cell survival and proliferation, often overexpressed in various cancers, including ovarian cancer.
- Targeting survivin offers a potential strategy for inhibiting cancer cell growth and inducing apoptosis.
Purpose of the Study:
- To investigate the efficacy of short hairpin RNA (shRNA) targeting survivin in ovarian cancer.
- To evaluate the impact of survivin inhibition on ovarian cancer cell behavior in vitro and in vivo.
Main Methods:
- Transfection of SKOV3 ovarian cancer cells with survivin-targeting shRNA.
- Assessment of survivin expression, apoptosis (using TEM, flow cytometry, TUNEL), and cell proliferation (MTT assay).
- Evaluation of tumor growth inhibition in a murine ovarian cancer xenograft model treated with survivin-targeting shRNA.
Main Results:
- Survivin-targeting shRNA significantly increased apoptosis and reduced proliferation in SKOV3 cells.
- Reduced survivin expression was observed at the molecular level in treated cells.
- In vivo, shRNA treatment markedly inhibited ovarian cancer xenograft growth with no apparent side effects.
Conclusions:
- shRNA targeting survivin demonstrates significant potential as a therapeutic agent for ovarian cancer.
- Inhibition of survivin through shRNA is a viable strategy for controlling ovarian cancer progression.
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