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Updated: Feb 22, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
MicroRNA-509-5p functions as an anti-oncogene in breast cancer via targeting SOD2
1Breast Center, Affiliated Hospital of Qingdao University, Qingdao, P.R. China. qdsongyh@163.com.
Objective:
Breast cancer is one of the most common malignant tumors in women worldwide. Considering the poor therapeutic effect of breast cancer, we are supposed to dissect the functioning mode of miR-509-5p on breast cancer cell growth and metastasis, providing therapeutic targets for breast cancer.
Patients And Methods:
Quantitative Real-time PCR (qRT-PCR) assay was employed to detect miR-509-5p expression level. CCK8 assay and colony formation assay were incorporated to assess cell viability and proliferation capacities. Cell migration and invasion assay were performed to investigate metastasis capacity of breast cancer cells. Flow cytometry was used to identify cell apoptosis and cell cycle distribution. Protein levels were assessed by Western blotting assay. The target gene was predicted and verified by bioinformatics analysis and luciferase assay.
Results:
MiR-509-5p was obviously downregulated in breast cancer tissues when compared with pericarcinomatous tissues (n=76). Overexpressed miR-509-5p could attenuate breast cancer cell viability, proliferation, migration and invasion capacities, as well as promote cell apoptosis and induce cell cycle arrest at G0/G1 phase. Superoxide dismutase 2 (SOD2) was chosen as the target gene of miR-509-5p by bioinformatic analysis and Luciferase reporter assay. Moreover, restoration of SOD2 could rescue tumor suppression role of miR-509-5p on breast cancer tumorigenesis.
Conclusions:
MiR-509-5p exerted tumor-suppressive effects on breast cancer progression and metastasis via targeting SOD2 in vitro, which provided an innovative and candidate target for diagnose and treatment of breast cancer.
Insights
MicroRNA-509-5p (miR-509-5p) acts as a tumor suppressor in breast cancer by inhibiting cell growth and metastasis. Targeting miR-509-5p and its downstream effector, SOD2, offers a potential therapeutic strategy for breast cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Breast cancer is a leading cause of cancer-related mortality in women globally.
- Existing therapies for breast cancer often have limited efficacy, necessitating novel therapeutic targets.
- Understanding the molecular mechanisms underlying breast cancer progression is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of microRNA-509-5p (miR-509-5p) in regulating breast cancer cell growth and metastasis.
- To identify potential therapeutic targets for breast cancer treatment based on miR-509-5p function.
Main Methods:
- Quantitative Real-time PCR (qRT-PCR) to measure miR-509-5p expression.
- Cell viability, proliferation, migration, invasion, apoptosis, and cell cycle assays (CCK8, colony formation, migration/invasion assays, flow cytometry).
- Western blotting for protein analysis, bioinformatics, and luciferase assays to identify and validate miR-509-5p targets.
Main Results:
- miR-509-5p was significantly downregulated in breast cancer tissues.
- Overexpression of miR-509-5p suppressed breast cancer cell viability, proliferation, migration, and invasion.
- miR-509-5p promoted apoptosis and induced G0/G1 cell cycle arrest.
- Superoxide dismutase 2 (SOD2) was identified as a direct target of miR-509-5p.
- Restoring SOD2 expression reversed the tumor-suppressive effects of miR-509-5p.
Conclusions:
- miR-509-5p exhibits tumor-suppressive properties against breast cancer progression and metastasis by targeting SOD2.
- miR-509-5p serves as a potential diagnostic and therapeutic target for breast cancer.
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