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Updated: Feb 10, 2026

DNA Vector-based RNA Interference to Study Gene Function in Cancer
Published on: June 4, 2012
[Effects of stromal interaction molecule 1 RNA interference on the cell proliferation and apoptosis in human
1Department of Otolaryngology, Qinghai University Affiliated Hospital, Xining, 810001, China.
Abstract:
Objective:To study the effects of stromal interaction molecule 1 (STIM1) RNA interference on cell proliferation, apoptosis, invasion and migration ability in vitro in human laryngeal cancer cells Hep-2. Method:Lentivirus transfection was used to realize the STIM1 RNA interference in human laryngeal cancer cells Hep-2. STIM1 RNA interference was verified by real-time PCR and western blotting. The cell proliferation was analyzed by CCK-8 method, Transwell chamber and wound scratch assay were used to detect cell invasion and migration ability, respectively. The cell apoptosis rate was evaluated by flow cytometry. The apoptotic proteins expression levels of caspase-3, Bax, Bcl-2, VEGF and MMP9 were detected by western blotting. Result:The gene expression levels of STIM1 mRNA and protein in human laryngeal cancer cells Hep-2 were significantly decreased after interference lentivirus transfection. After the interference of STIM1, the cell proliferation, invasion and migratory ability of Hep-2 cells in vitro declined (P<0.05). The cell apoptosis rate significantly increased after STIM1 RNA interference, along with the caspase-3 and Bax protein expression levels up-regulation, and the Bcl-2 expression levels down-regulation. The decrease of cell invasion and migratory ability was related with the down-regulation of VEGF and MMP9 protein expression. Conclusion:RNA interference of STIM1 in human laryngeal cancer cells Hep-2 inhibits the cell proliferation, invasion and migration ability in vitro, and enhances the cell apoptosis rate of Hep-2 cells.
Insights
Stromal interaction molecule 1 (STIM1) RNA interference significantly reduced laryngeal cancer cell proliferation, invasion, and migration. STIM1 knockdown also increased apoptosis, offering potential therapeutic targets for Hep-2 cells.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Laryngeal cancer poses a significant health challenge.
- Stromal interaction molecule 1 (STIM1) is implicated in various cellular processes.
- Understanding STIM1's role in laryngeal cancer is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the impact of STIM1 RNA interference on human laryngeal cancer Hep-2 cells.
- To assess the effects on cell proliferation, apoptosis, invasion, and migration in vitro.
- To explore the molecular mechanisms underlying STIM1's function in laryngeal cancer.
Main Methods:
- Lentivirus-mediated RNA interference was employed to silence STIM1 in Hep-2 cells.
- Quantitative real-time PCR and Western blotting confirmed STIM1 knockdown.
- Cell proliferation, invasion, migration, and apoptosis were analyzed using CCK-8, Transwell assays, scratch assays, and flow cytometry, respectively.
Main Results:
- STIM1 gene and protein expression were significantly reduced post-interference.
- Hep-2 cell proliferation, invasion, and migration abilities decreased (P<0.05).
- Apoptosis rate increased, with upregulated caspase-3 and Bax, and downregulated Bcl-2, VEGF, and MMP9.
Conclusions:
- STIM1 RNA interference effectively inhibits proliferation, invasion, and migration of human laryngeal cancer Hep-2 cells in vitro.
- Silencing STIM1 enhances apoptosis in Hep-2 cells.
- Targeting STIM1 presents a promising therapeutic strategy for laryngeal cancer.
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RNA Interference
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