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Updated: Oct 3, 2025

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
Published on: April 7, 2017
mir-204-5p Acts as a Tumor Suppressor by Targeting DNM2 in Osteosarcoma Cells
Liangliang Qu1, Zhongqiu Li2, Pinduan Liu1
1Department of Orthopedics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou 121001, Liaoning, China.
Abstract:
Osteosarcoma is a malignant bone tumor composed of interstitial cells. We aim to seek the function of mir-204-5p/DNM2 in osteosarcoma cells. From April 2017 to August 2019, 58 cases of cancer tissues and paracancer tissues were obtained from patients with osteosarcoma in our hospital. qPCR was used to detect mir-204-5p in excisional cancer tissues and paracarcinoma tissues of osteosarcoma patients. The overexpression vector of mir-204-5p was established and transfected into osteosarcoma cells, and the propagation, invasiveness, migration, and apoptosis of osteosarcoma cells were observed. StarBase was employed to forecast the binding site of mir-204-5p and DNM2. The targeting connection of mir-204-5p with DNM2 was detected via double luciferase reporter gene. mir-204-5p was lessened in osteosarcoma (p < 0.05). mir-204-5p overexpression suppressed propagation and accelerated apoptosis of osteosarcoma cells (p < 0.05). The results of double luciferase reporter gene revealed that the fluorescence activity of mir-204-5p was obviously declined when binding to DNM2 (p < 0.05). mir-204-5p functions as a tumor inhibitor by targeting DNM2 in osteosarcoma cells. Our research is helpful to provide new ideas for clinical treatment.
Insights
MicroRNA-204-5p (mir-204-5p) acts as a tumor suppressor in osteosarcoma. Its overexpression inhibits cancer cell growth and promotes apoptosis by targeting DNM2, offering potential new therapeutic strategies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma is a primary malignant bone tumor.
- Understanding the molecular mechanisms driving osteosarcoma progression is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the role of microRNA-204-5p (mir-204-5p) in osteosarcoma.
- To elucidate the functional relationship between mir-204-5p and DNM2 in osteosarcoma cells.
Main Methods:
- Quantitative real-time PCR (qPCR) to measure mir-204-5p expression in patient tissues.
- Transfection of osteosarcoma cells with mir-204-5p overexpression vectors.
- Assessment of cell proliferation, invasion, migration, and apoptosis.
- Bioinformatic prediction using StarBase and validation via dual-luciferase reporter assays to confirm mir-204-5p targeting of DNM2.
Main Results:
- Mir-204-5p expression was significantly downregulated in osteosarcoma tissues compared to adjacent non-cancerous tissues.
- Overexpression of mir-204-5p suppressed osteosarcoma cell proliferation and migration while promoting apoptosis.
- Dual-luciferase reporter assays confirmed that mir-204-5p directly targets DNM2, indicated by reduced fluorescence activity upon binding.
Conclusions:
- Mir-204-5p functions as a tumor suppressor in osteosarcoma.
- The tumor-inhibitory effect of mir-204-5p is mediated through its targeting of DNM2.
- These findings suggest mir-204-5p/DNM2 axis as a potential therapeutic target for osteosarcoma treatment.
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