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Effect of PTEN antisense oligonucleotide on oesophageal squamous cell carcinoma cell lines
1Department of Oncology, First Affiliated Hospital, Zhengzhou University, Zhengzhou, China.
Objective:
To investigate the effects of a phosphatase and tensin homologue (PTEN) antisense oligonucleotide on PTEN and mammalian target of rapamycin (mTOR) mRNA and protein, cell proliferation and apoptosis in oesophageal squamous cell carcinoma (OCSS) cell lines.
Methods:
EC9706 and EC1 cells were transfected with PTEN antisense oligonucleotide, sense oligonucleotide or nonsense oligonucleotide. Cell proliferation and apoptosis were quantified. Immuno cyto chemistry and in situ hybridization were used to determine PTEN and mTOR protein and mRNA levels, respectively.
Results:
Transfection with PTEN antisense oligonucleotide dose- and time-dependently enhanced cell proliferation and inhibited apoptosis in both EC9706 and EC1 cells. PTEN mRNA and protein were significantly downregulated, and mTOR protein and mRNA were significantly upregulated.
Conclusion:
These data suggest that PTEN is an important tumour suppressor gene in the development of OSCC.
Insights
Targeting phosphatase and tensin homologue (PTEN) with antisense oligonucleotides reduced PTEN levels, increased proliferation, and inhibited apoptosis in esophageal squamous cell carcinoma (OSCC) cells, suggesting PTEN
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Esophageal squamous cell carcinoma (OSCC) is a significant global health concern.
- The role of tumor suppressor genes, like PTEN, in OSCC development requires further elucidation.
- Understanding the PTEN/mTOR pathway is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the impact of PTEN modulation on OSCC cell lines.
- To analyze the effects of PTEN antisense oligonucleotide on PTEN and mTOR expression.
- To assess the influence on cell proliferation and apoptosis in OSCC.
Main Methods:
- EC9706 and EC1 OSCC cell lines were utilized.
- Cells were transfected with PTEN antisense, sense, or nonsense oligonucleotides.
- PTEN and mTOR mRNA/protein levels were quantified using in situ hybridization and immunocytochemistry, alongside proliferation and apoptosis assays.
Main Results:
- PTEN antisense oligonucleotide treatment led to dose- and time-dependent increases in cell proliferation and decreases in apoptosis.
- Significant downregulation of PTEN mRNA and protein was observed.
- Concurrently, a significant upregulation of mTOR mRNA and protein was detected.
Conclusions:
- PTEN plays a critical role as a tumor suppressor in the context of OSCC.
- Modulating PTEN levels impacts key cellular processes like proliferation and apoptosis in OSCC.
- The findings highlight the PTEN/mTOR pathway as a potential therapeutic target in OSCC.
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