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Updated: Jun 12, 2025

MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR qPCR
Published on: May 16, 2012
Increasing prostate cancer radiosensitivity by miR-7-5p knockdown of anti-apoptotic genes
Leili Darvish1, Mohammad-Taghi Bahreyni-Toossi2, Seyed Hamid Aghaee-Bakhtiari3
1Mother and Child Welfare Research Center, Hormozgan University of Medical Sciences, Bandar Abbas, Iran; Department of Radiology, Faculty of Paramedicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Abstract:
Despite the success of radiotherapy for prostate cancer treatment, the recent discovery of radiation resistance prevents it from reaching its full potential. This study aims to use hsa-miR-7-5p for the expression of anti-apoptotic genes. The search for anti-apoptotic genes was carried out through databases. The selected genes included XIAP, MCL1, REL, and BIRC3. Our selection was based on the best miRNA because it has a greater impact on genes. The second step involved transfecting the miRNA into a prostate cancer cell line. Subsequently, radiosensitivity was tested using real-time PCR, clonogenic assay, and annexin V flow cytometry. The highest apoptosis rate in the transfected cells was at 0 Gy in hsa-miR-7-5p (28.88 ± 0.80), plenti III (18.81 ± 0.59), and the control group (4.10 ± 1.52) (P<0.001). Also, its rate was at 4 Gy in hsa-miR-7-5p (36.11 ± 1.93), plenti III (26.42 ± 0.42), and the control group (8.79 ± 2.29) (P<0.001). This study showed a decreasing trend in survival with increasing doses. Suppression of anti-apoptotic genes, including XIAP, MCL1, Birc3, and REL, enhanced radiosensitivity by increasing the expression of hsa-miR-7-5p in the PC3 and LNCaP cell lines. Hsa-miR-7-5p is a miRNA that can suppress the expression of anti-apoptotic genes and thus plays an essential role in the process of cell apoptosis. Targeting genes that are associated with apoptosis could potentially enhance the efficacy of treatments for patients with prostate cancer.
Insights
This study shows that hsa-miR-7-5p can overcome radiation resistance in prostate cancer by suppressing anti-apoptotic genes. This enhances radiosensitivity and increases apoptosis, offering a potential new treatment strategy.
Area of Science:
- Oncology
- Molecular Biology
- Radiotherapy Research
Background:
- Prostate cancer radiotherapy is limited by radiation resistance.
- Identifying mechanisms to overcome resistance is crucial for improving treatment efficacy.
Purpose of the Study:
- To investigate the role of hsa-miR-7-5p in overcoming radiation resistance in prostate cancer.
- To determine if hsa-miR-7-5p can suppress anti-apoptotic genes and enhance radiosensitivity.
Main Methods:
- Bioinformatic search for anti-apoptotic genes (XIAP, MCL1, REL, BIRC3) targeted by hsa-miR-7-5p.
- Transfection of hsa-miR-7-5p into prostate cancer cell lines (PC3 and LNCaP).
- Assessment of radiosensitivity using real-time PCR, clonogenic assay, and annexin V flow cytometry.
Main Results:
- hsa-miR-7-5p transfection significantly increased apoptosis rates at 0 Gy and 4 Gy compared to control groups.
- Suppression of anti-apoptotic genes XIAP, MCL1, Birc3, and REL was observed.
- Enhanced radiosensitivity was demonstrated in PC3 and LNCaP cell lines with increased hsa-miR-7-5p expression.
Conclusions:
- hsa-miR-7-5p effectively suppresses anti-apoptotic gene expression, promoting apoptosis in prostate cancer cells.
- Targeting anti-apoptotic genes with hsa-miR-7-5p represents a promising strategy to enhance prostate cancer radiotherapy efficacy.
- This miRNA plays a key role in regulating apoptosis and could be a therapeutic target.
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