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Updated: Apr 25, 2026

Assessment of Selective mRNA Translation in Mammalian Cells by Polysome Profiling
Published on: October 28, 2014
Specific siRNA inhibits XIAP expression in human endometrial carcinoma cell apoptosis
Duo Yin1, Ning Wang, Shu-lan Zhang
1Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, 36 Sanhao Road, Heping District, Shenyang, 110004, Liaoning Province, China.
Abstract:
The aim of the study was to investigate the inhibitory effects of RNA interference on XIAP gene expression of human endometrial carcinoma RL95-2 cell and the cell apoptosis. Specific small interference RNA (siRNA) of XIAP was designed and composed. Transfection of siRNA was conducted in endometrial carcinoma cell line RL95-2. The XIAP gene mRNA was assessed by real-time PCR and the change of XIAP protein was assessed with Western Blotting. The cell proliferation and apoptosis was assessed by MTT and flow cytometry methods. After transfection of siRNA specifically targeting XIAP, the relative fold of mRNA transfection in the specific transfection group was (0.04 ± 0.06) and the relative protein expression was (0.590 ± 0.178), which was significantly decreased when compared with the control group (P < 0.05); the cell growth inhibition rate in the transfection group was (47.86 ± 4.46)%, which was significantly increased when compared to the control group (P < 0.05). In vitro experiment showed that synthetic siRNA could effectively inhibit the transfection and expression of XIAP gene of human endometrial carcinoma RL95-2 cell at the mRNA level and protein level, thus significantly promote the apoptosis of endometrial carcinoma cell. The mechanisms involved in the apoptosis still require further investigation.
Insights
Small interfering RNA (siRNA) effectively inhibited X-linked inhibitor of apoptosis protein (XIAP) gene expression in human endometrial cancer cells. This inhibition significantly promoted cancer cell apoptosis, suggesting a potential therapeutic strategy.
Area of Science:
- Molecular Biology
- Oncology
- Gene Therapy
Background:
- Endometrial carcinoma is a significant gynecological malignancy.
- X-linked inhibitor of apoptosis protein (XIAP) is implicated in cancer cell survival and resistance to apoptosis.
- Targeting XIAP offers a potential strategy for endometrial cancer treatment.
Purpose of the Study:
- To investigate the inhibitory effects of RNA interference targeting XIAP on human endometrial carcinoma RL95-2 cells.
- To assess the impact of XIAP gene silencing on cell apoptosis and proliferation.
Main Methods:
- Design and synthesis of small interfering RNA (siRNA) specific for XIAP.
- Transfection of RL95-2 cells with XIAP siRNA.
- Quantitative assessment of XIAP mRNA levels using real-time PCR.
- Assessment of XIAP protein expression via Western Blotting.
- Evaluation of cell proliferation and apoptosis using MTT assay and flow cytometry.
Main Results:
- XIAP siRNA significantly reduced XIAP mRNA and protein expression in RL95-2 cells (P < 0.05).
- A significant increase in cell growth inhibition rate (47.86 ± 4.46%) was observed in the siRNA-treated group (P < 0.05).
- Flow cytometry analysis indicated a significant promotion of apoptosis in endometrial carcinoma cells following XIAP gene silencing.
Conclusions:
- Synthetic siRNA effectively inhibits XIAP gene expression at both mRNA and protein levels in human endometrial carcinoma RL95-2 cells.
- XIAP gene silencing significantly promotes apoptosis of endometrial carcinoma cells.
- Further investigation is warranted to elucidate the precise mechanisms underlying XIAP-mediated apoptosis in this context.
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