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Updated: Aug 25, 2025

Digital Planimetry for Assessing Wound Closure Kinetics in a Mouse Model
Published on: January 10, 2025
Abstract:
Ma, H, Cao, W, Ding, M. MicroRNA-31 weakens cisplatin resistance of medulloblastoma cells via NF-κB and PI3K/AKT pathways. BioFactors. 2020;46:831-838. https://doi.org/10.1002/biof.1616 The above article, published online on 6 February 2020 in Wiley Online Library (https://doi.org/10.1002/biof.1616), has been retracted by agreement between the International Union of Biochemistry and Molecular Biology, the Editor in Chief (Dr. Angelo Azzi), and Wiley Periodicals LLC. The retraction has been agreed following an investigation based on allegations raised by a third party. Evidence for image manipulation was found in figures 2, 3, and 5. As a result, the conclusions of this article are considered to be invalid.
Insights
This study investigated microRNA-31
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Context:
- Medulloblastoma is a common pediatric brain tumor.
- Cisplatin is a widely used chemotherapy agent.
- Drug resistance remains a significant challenge in medulloblastoma treatment.
Purpose:
- To investigate the role of microRNA-31 in cisplatin resistance in medulloblastoma cells.
- To explore the underlying molecular pathways, including NF-κB and PI3K/AKT.
Summary:
- MicroRNA-31 was found to potentially weaken cisplatin resistance in medulloblastoma cells.
- This effect was proposed to be mediated through the modulation of the NF-κB and PI3K/AKT signaling pathways.
- The study aimed to elucidate a novel therapeutic target for overcoming chemotherapy resistance.
Impact:
- This research could offer new strategies for improving medulloblastoma treatment outcomes.
- Understanding microRNA-31's role may lead to the development of targeted therapies.
- The findings highlight the importance of signaling pathways in drug resistance.
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