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Quantitative PCR-based Assay to Measure Sonic Hedgehog Signaling in Cellular Model of Ciliogenesis
Published on: January 31, 2025
Mir-326 potentiates radiosensitivity of cervical squamous cell carcinoma through downregulating SMO expression in the
Junqin Zhang1, Yaxing Li2, Yanan Ren1
1Department of Gynecology, Hebei General Hospital, Shijiazhuang, China.
Background:
Radiotherapy resistance affects the therapeutic effect of cervical squamous cell carcinoma (CSCC). Smoothened (Smo) is an anticancer target of the Hedgehog (Hh) pathway and its mutation is related to drug resistance.
Objective:
To explore the roles of miR-326 and Smoothened (SMO) on radiation resistance in patients with cervical carcinoma.
Methods:
Expression of miR-326 and SMO in cervical cancer tissue and radioresistant cell lines were analyzed. The radiation response with the expression of miR-326 was evaluated in tissue and cells. Bioinformatics analysis and literature review were performed to explore the target of miR-326. The regulation of miR-326 to SMO mRNA was verified through the dual-luciferase reporter assay.
Results:
Patients with poor radiation response have lower miR-326 and higher SMO expression. Upregulation of miR-326 decreased SMO expression and its downstream proteins but does not affect the proliferation of CSCC cells. The upregulation of miR-326 increased radiation sensitivity of the CSCC cell through downregulating SMO and its downstream proteins in the Hedgehog (Hh) signaling pathway.
Conclusions:
miR-326 may predict the treatment response to radiation, and upregulating miR-326 may improve the treatment response to radiation.
Insights
Upregulating miR-326 enhances radiation sensitivity in cervical squamous cell carcinoma (CSCC) by targeting Smoothened (SMO). This microRNA may predict and improve patient response to radiotherapy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Radiotherapy resistance is a significant challenge in treating cervical squamous cell carcinoma (CSCC).
- The Hedgehog (Hh) pathway, particularly Smoothened (SMO), is implicated in drug resistance.
- Understanding molecular mechanisms is crucial for overcoming treatment resistance.
Purpose of the Study:
- To investigate the roles of miR-326 and SMO in the context of radiation resistance in cervical cancer.
- To explore the relationship between miR-326 expression and radiation response in CSCC patients.
Main Methods:
- Analysis of miR-326 and SMO expression in cervical cancer tissues and radioresistant cell lines.
- Evaluation of radiation response correlated with miR-326 levels.
- Bioinformatics analysis and dual-luciferase reporter assays to confirm miR-326 targeting of SMO mRNA.
Main Results:
- Lower miR-326 and higher SMO expression were observed in patients with poor radiation response.
- Upregulation of miR-326 led to decreased SMO and downstream protein expression.
- Increased miR-326 enhanced CSCC cell radiosensitivity by downregulating the SMO/Hh pathway.
Conclusions:
- miR-326 expression levels can potentially predict patient response to radiotherapy.
- Therapeutic strategies involving the upregulation of miR-326 may improve treatment outcomes for cervical cancer patients receiving radiation.
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