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Prognostic Value of miR-137 in Children with Medulloblastoma and its Regulatory Effect on Tumor Progression
Wenyuan Ji1,2,3,4, Xuan Zhe1,2,3,4, Lusheng Li1,2,3,4
1Department of Neurosurgery, Children's Hospital of Chongqing Medical University, No. 136, 2nd Zhongshan Road, Yuzhong District, Chongqing, 400014, People's Republic of China.
Abstract:
Medulloblastoma is a malignant tumor with high incidence and poor prognosis in adolescents and children. MicroRNA-137 (miR-137) has been found to be abnormally expressed in cancers such as pancreatic cancer. The purpose of this study is to explore the expression of miR-137 in MB and its role in cell physiological activities to determine the significance of miR-137 in the prognosis of MB. First, the expression of miR-137 in MB tissues and cell lines was analyzed by qRT-PCR. Then the Kaplan-Meier survival curve was used to analyze the significance of miR-137 expression in the prognosis, and the Cox regression model was used to explore the correlation between miR-137 expression and clinical characteristics. The effects of miR-137 on MB cell activities were analyzed by MTT assay, Transwell assays, and flow cytometry. It can be concluded from the results that the expression of miR-137 is down-regulated in MB tissues and cells. The down-regulation of miR-137 was significantly related to the poor prognosis of MB, and significantly related to clinical indicators. Up-regulated miR-137 inhibited cell proliferation, migration, invasion, and cell cycle progression, as well as induced cell apoptosis by targeting KDM1A. This study can conclude that miR-137 may be used as a prognostic biomarker of MB.
Insights
MicroRNA-137 (miR-137) is down-regulated in medulloblastoma (MB), a pediatric cancer. Restoring miR-137 levels inhibits MB cell growth and progression, suggesting its potential as a prognostic biomarker.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Medulloblastoma (MB) is a highly aggressive pediatric brain tumor with limited treatment options.
- MicroRNA-137 (miR-137) dysregulation is implicated in various cancers, but its role in MB remains unclear.
Purpose of the Study:
- To investigate the expression levels of miR-137 in medulloblastoma.
- To determine the prognostic significance of miR-137 in MB.
- To elucidate the functional role of miR-137 in MB cell behavior.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) for miR-137 expression analysis in MB tissues and cell lines.
- Kaplan-Meier survival analysis and Cox regression modeling to assess prognostic value and clinical correlations.
- In vitro assays including MTT, Transwell, and flow cytometry to evaluate the impact of miR-137 on cell proliferation, migration, invasion, cell cycle, and apoptosis.
Main Results:
- miR-137 expression was significantly downregulated in MB tissues and cell lines compared to normal controls.
- Lower miR-137 expression correlated with poorer prognosis and was associated with specific clinical characteristics in MB patients.
- Upregulation of miR-137 suppressed MB cell proliferation, migration, and invasion, while promoting apoptosis and inhibiting cell cycle progression, partly through targeting KDM1A.
Conclusions:
- miR-137 is a tumor suppressor microRNA in medulloblastoma.
- Downregulation of miR-137 is a significant indicator of poor prognosis in medulloblastoma.
- miR-137 holds potential as a valuable prognostic biomarker for medulloblastoma.
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