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Updated: Aug 15, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Silencing circUSP48 suppresses osteosarcoma progression by regulating the miR-335/ smad nuclear interacting protein 1
Yue Luo1, Bo Yang1, Xiaopin Yuan1
1Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, China.
Background:
Circular RNAs (circRNAs) can have a critical function in the multi-processes of osteosarcoma (OS). Nevertheless, whether circUSP48 is involved in OS progression remains unclear.
Methods:
In the current work, the expression of circUSP48, miR-335 and SNIP1 in OS cell lines and tissues were evaluated using qRT-PCR. Then, Sanger sequencing, RNase R treatment and FISH assay were performed for circUSP48 validation. Furthermore, the function and potential mechanisms of circUSP48 in OS were investigated by performing loss-of-function experiments.
Results:
Silencing circUSP48 could suppress proliferation, invasion as well as migration of OS cells in vitro, also inhibiting the growth of tumor in vivo. Importantly, circUSP48 promoted OS malignancy by sponging miR-335 to upregulate SNIP1.
Conclusion:
Overall, these findings suggested that circUSP48 acted as an oncogene in OS, which might become a new target for OS therapy.
Insights
Circular USP 48 (circUSP48) promotes osteosarcoma (OS) progression by sponging miR-335 to increase SNIP1. Silencing circUSP48 inhibits OS cell proliferation, invasion, migration, and tumor growth, suggesting circUSP48 as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) play roles in osteosarcoma (OS) development.
- The specific role of circUSP48 in OS progression is currently unknown.
Purpose of the Study:
- To investigate the function and mechanism of circUSP48 in osteosarcoma.
- To determine if circUSP48 acts as an oncogene in OS.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess expression levels of circUSP48, miR-335, and SNIP1.
- circUSP48 validation using Sanger sequencing, RNase R treatment, and FISH assays.
- Loss-of-function experiments to evaluate circUSP48's role in OS cell lines and in vivo tumor growth.
Main Results:
- Silencing circUSP48 suppressed proliferation, invasion, and migration of OS cells in vitro.
- circUSP48 inhibition also reduced tumor growth in vivo.
- circUSP48 promotes OS malignancy by sponging miR-335, leading to SNIP1 upregulation.
Conclusions:
- circUSP48 functions as an oncogene in osteosarcoma.
- circUSP48 may represent a novel therapeutic target for osteosarcoma treatment.
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