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Circ_0105346 Knockdown Inhibits Osteosarcoma Development via Regulating miR-1182/WNT7B Axis
Jinbao Liu1, Xiaoyang Li1, Liang Yue2
1Department of Orthopaedics, The First Clinical Medical School, Shandong University of Traditional Chinese Medicine, Jinan 250011, People's Republic of China.
Cancer Management and Research
|January 28, 2021
Summary
Circular RNA circ_0105346 promotes osteosarcoma progression by upregulating WNT7B via sponging miR-1182. Knockdown of circ_0105346 inhibits tumor growth, offering a potential therapeutic target for osteosarcoma.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma (OS) is a prevalent bone cancer in pediatric patients.
- Circular RNAs (circRNAs) are increasingly recognized for their roles in cancer development.
- This study investigates the function of circ_0105346 in OS.
Purpose of the Study:
- To elucidate the role of circRNA circ_0105346 in osteosarcoma (OS) development.
- To explore the underlying molecular mechanism involving microRNA (miR)-1182 and wingless-type MMTV integration site family 7B (WNT7B).
Main Methods:
- Quantitative reverse transcription PCR (qRT-PCR) and Western blot to assess expression levels.
- Cell proliferation, apoptosis, cell cycle, migration, and invasion assays (MTT, flow cytometry, transwell, wound healing).
- Dual-luciferase reporter, RNA immunoprecipitation (RIP), and pull-down assays to confirm molecular interactions; in vivo mouse xenograft model.
Main Results:
- Circ_0105346 and WNT7B were upregulated, while miR-1182 was downregulated in OS tissues and cells.
- Circ_0105346 knockdown inhibited OS cell proliferation, migration, invasion, and glycolysis, and promoted apoptosis.
- Circ_0105346 targets miR-1182, which targets WNT7B, establishing a circ_0105346/miR-1182/WNT7B regulatory axis; tumor growth was inhibited in vivo.
Conclusions:
- Circ_0105346 knockdown suppresses osteosarcoma progression.
- The circ_0105346/miR-1182/WNT7B axis is a key regulator of OS development.
- Circ_0105346 represents a potential therapeutic target for osteosarcoma.
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