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MicroRNA-496 suppresses tumor cell proliferation by targeting BDNF in osteosarcoma
Jing Ye1, Wei Xie1, Yunzhou Zuo1
1Department of Orthopedics, Hubei 672 Orthopedics Hospital of Integrated Chinese and Western Medicine, Wuhan, Hubei 430079, P.R. China.
Abstract:
MicroRNAs (miRNAs) are integrally involved in biological and pathobiological development. Many studies have demonstrated the abnormal expression of microRNA-496 (miR-496) in various human malignant tumors. The present study was designed to investigate the functions and the underlying mechanisms of miR-496 in osteosarcoma (OS) progression. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to determine the expression of miR-496 in OS tissues and cell lines. Luciferase activity was used to confirm the interaction between miR-496 and brain derived neurotrophic factor (BDNF), a downstream gene of miR-496. RT-qPCR was also used to quantify BDNF mRNA expression, and the BDNF protein expression level was detected by western blot analysis. In addition, the Cell Counting Kit-8 (CCK-8) was used to detect cell viability. The results revealed that the level of miR-496 expression was significantly reduced in osteosarcoma tissues and cell lines. BDNF was verified to be a direct target gene of miR-496 and was found to be negatively regulated by miR-496. Overall, it was demonstrated that miR-496 inhibits osteosarcoma cell proliferation via inhibition of BDNF. Thus, the miR-496/BDNF axis may be a novel strategy for the clinical treatment of OS.
Insights
MicroRNA-496 (miR-496) is reduced in osteosarcoma (OS). It inhibits OS cell proliferation by targeting brain-derived neurotrophic factor (BDNF), suggesting a new treatment strategy.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- MicroRNAs (miRNAs) regulate biological and pathobiological development.
- Aberrant microRNA-496 (miR-496) expression is observed in various human cancers.
- The role of miR-496 in osteosarcoma (OS) progression requires further investigation.
Purpose of the Study:
- To investigate the function of miR-496 in osteosarcoma (OS) progression.
- To elucidate the underlying molecular mechanisms of miR-496 in OS.
- To identify potential therapeutic targets for OS treatment.
Main Methods:
- Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) for gene expression analysis.
- Luciferase reporter assays to confirm direct gene targeting.
- Western blot and CCK-8 assays to assess protein levels and cell viability.
Main Results:
- miR-496 expression was significantly downregulated in osteosarcoma tissues and cell lines.
- Brain-derived neurotrophic factor (BDNF) was identified as a direct target gene of miR-496.
- miR-496 inhibited osteosarcoma cell proliferation by downregulating BDNF expression.
Conclusions:
- miR-496 acts as a tumor suppressor in osteosarcoma.
- The miR-496/BDNF axis represents a potential therapeutic target for osteosarcoma.
- Further research into the miR-496/BDNF pathway could lead to novel clinical strategies for OS treatment.
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