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Updated: May 16, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
[Down-regulation of miR-21 expression enhances the radiosensitivity of TE-1 cells in vitro]
Xiaoqing Li1, Xin Chen, Shan Huang
1Department of Radiotherapy, First Affiliated Hospital of Xi'an Jiaotong University College of Medicine, Xi'an, China. Lixiaoqing_1221@126.com
Objective:
To study the effect of miR-21 down-regulation on the radiosensitivity of TE-1 cells in vitro.
Methods:
TE-1 cells were transfected via lentivirus with a vector containing the antisense oligonucleotides of miR21, and the subclones with stable down-regulation of miR21 expression were selected with puromycin and designated as TE-1-miR21(-), whose expression level of miR21 was determined using real-time quantitative PCR. The radiosensitivity of TE-1 and TE-1-miR21(-) cells were evaluated with colony formation assay, and the expressions of β-catenin was determined using Western blotting and RT-PCR. Flow cytometry was used to analyze the proportion of p75NTR(+) cells in TE-1 and TE-1-miR21(-) cells.
Results:
A cell subclone stably expressing a low level of miR21 was obtained and verified by real-time quantitative PCR. Colony formation assay showed an enhanced the radiosensitivity of TE-1-miR21(-) cells compared to parental TE-1 cells. RT-PCR revealed no significant changes in β-catenin mRNA expression in TE-1-miR21(-) cells, whereas its β-catenin protein expression was markedly suppressed by high-dose (8 and 10 Gy) irradiation. Flow cytometry assay showed a decreased proportion of p75NTR(+) cells in TE-1-miR21(-) cells compared to that in TE-1 cells.
Conclusion:
Down-regulation of miR21 can enhance the radiosensitivity of TE-1 cells, which might result from the inactivation of wnt/β-catenin signal pathway and a decreased p75NTR(+) cell proportion.
Insights
Down-regulating miR-21 enhances radiosensitivity in TE-1 cells. This effect may involve the wnt/β-catenin pathway and reduced p75NTR positive cells, offering potential therapeutic strategies.
Area of Science:
- Molecular Biology
- Oncology
- Cell Biology
Context:
- MicroRNA-21 (miR-21) is implicated in cancer progression and radioresistance.
- Esophageal squamous cell carcinoma (TE-1 cells) exhibit varying responses to radiotherapy.
- Understanding miR-21's role is crucial for improving cancer treatment efficacy.
Purpose:
- To investigate the impact of miR-21 down-regulation on the radiosensitivity of TE-1 cells.
- To explore the underlying mechanisms, including the wnt/β-catenin pathway and p75NTR expression.
Summary:
- TE-1 cells with stably down-regulated miR-21 (TE-1-miR21(-)) were generated using lentiviral transfection.
- Radiosensitivity was assessed via colony formation assay, showing enhanced sensitivity in TE-1-miR21(-) cells.
- While β-catenin mRNA levels remained unchanged, protein expression was suppressed by irradiation; p75NTR positive cell proportion decreased.
Impact:
- miR-21 down-regulation significantly enhances the radiosensitivity of TE-1 cells.
- This enhancement is potentially mediated by the inactivation of the wnt/β-catenin signaling pathway.
- A reduced proportion of p75NTR positive cells may also contribute to increased radiosensitivity, suggesting novel therapeutic targets.
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