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Updated: Mar 2, 2026

Utilizing Murine Inducible Telomerase Alleles in the Studies of Tissue Degeneration/Regeneration and Cancer
Published on: April 13, 2015
[Effect of hTERT antisense oligodeoxynucleotide on telomerase activity in bladder cancer cells in vitro]
1Department of Urology, Lanzhou General Hospital of Lanzhou Command, Lanzhou 730050, China. gxd58038@yahoo.com.cn
Objective:
To investigate the effect of hTERT antisense oligodeoxynucleotide on telomerase activity in bladder cancer cells.
Methods:
Antisense phosphorothioate oligodeoxynucleotide (AS PS-ODN) was synthesized and purified. Telomerase activity was measured by telomerase PCR ELISA kit. hTERT mRNA expression was detected by reverse transcription-polymerase chain reaction (RT-PCR), and hTERT protein by immunohistochemistry and flow cytometry.
Results:
Telomerase activity was decreased in T24 cells 48 h after treatment with AS PS-ODN, and was significantly inhibited at 72 h.
Conclusion:
AS PS-ODN can significantly inhibit telomerase activity by down-regulating hTERT mRNA and protein expression in bladder cancer cells.
Insights
This study shows that antisense phosphorothioate oligodeoxynucleotide (AS PS-ODN) effectively reduces telomerase activity in bladder cancer cells by targeting hTERT expression.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Context:
- Telomerase is a key enzyme in cancer development and progression.
- Bladder cancer exhibits high telomerase activity, making it a therapeutic target.
- Antisense technology offers a targeted approach to inhibit specific gene expression.
Purpose:
- To evaluate the efficacy of hTERT antisense oligodeoxynucleotide (AS PS-ODN) in inhibiting telomerase activity.
- To assess the impact of AS PS-ODN on hTERT mRNA and protein levels in bladder cancer cells.
Summary:
- AS PS-ODN was synthesized and its effect on telomerase activity was measured using a PCR ELISA kit.
- hTERT mRNA and protein expression were analyzed via RT-PCR, immunohistochemistry, and flow cytometry.
- Treatment with AS PS-ODN led to a significant decrease in telomerase activity, hTERT mRNA, and protein levels in T24 bladder cancer cells within 72 hours.
Impact:
- Demonstrates the potential of AS PS-ODN as a therapeutic agent for bladder cancer.
- Provides a molecular mechanism for telomerase inhibition in cancer cells.
- Highlights the role of hTERT downregulation in controlling cancer cell proliferation.
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