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Updated: Nov 7, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
CircRNA EPB41L2 inhibits tumorigenicity of lung adenocarcinoma through regulating CDH4 by miR-211-5p
1Department of Respiratory Medicine, Huaihe Hospital of Henan University, Kaifeng, China.
Abstract:
The article "CircRNA EPB41L2 inhibits tumorigenicity of lung adenocarcinoma through regulating CDH4 by miR-211-5p, by S.-J. Zhang, J. Ma, J.-C. Wu, Z.-Z. Hao, Y.-N. Zhang, Y.-J. Zhang, published in Eur Rev Med Pharmacol Sci 2020; 24 (7): 3749-3760-DOI: 10.26355/eurrev_202004_20839-PMID: 32329852" has been withdrawn from the authors due to inaccuracies and mistakes. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/20839.
Insights
This study on lung adenocarcinoma has been withdrawn due to inaccuracies. The research investigated circular RNA EPB41L2
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Lung adenocarcinoma (LUAD) is a major cause of cancer-related mortality.
- Circular RNAs (circRNAs) are emerging as critical regulators in various cancers.
- The role of circRNA EPB41L2 in LUAD tumorigenesis requires further elucidation.
Purpose of the Study:
- To investigate the function of circRNA EPB41L2 in lung adenocarcinoma.
- To explore the regulatory mechanism of circRNA EPB41L2 involving miR-211-5p and CDH4.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess gene and microRNA expression.
- Western blotting to detect protein levels.
- Cell proliferation and migration assays to evaluate tumorigenicity.
Main Results:
- CircRNA EPB41L2 was found to be downregulated in LUAD tissues.
- Overexpression of circRNA EPB41L2 suppressed LUAD cell proliferation and migration.
- CircRNA EPB41L2 acted as a sponge for miR-211-5p, thereby regulating CDH4 expression.
Conclusions:
- CircRNA EPB41L2 functions as a tumor suppressor in lung adenocarcinoma.
- The circRNA EPB41L2/miR-211-5p/CDH4 axis represents a potential therapeutic target for LUAD.
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