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Updated: Dec 6, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MiR-16 inhibits pituitary adenoma cell proliferation via the suppression of ERK/MAPK signal pathway
1Department of Neurosurgery, the Second Affiliated Hospital of Bengbu Medical College, Bengbu, Anhui, People's Republic of China.
Abstract:
Since this article has been suspected of research misconduct and the corresponding authors did not respond to our request to prove originality of data and figures, "MiR-16 inhibits pituitary adenoma cell proliferation via the suppression of ERK/MAPK signal pathway, by D.-W. Wang, Y.-Q. Wang, H.-S. Shu, published in Eur Rev Med Pharmacol Sci 2018; 22 (5): 1241-1248-DOI: 10.26355/eurrev_201803_14464-PMID: 29565480" has been withdrawn. The Publisher apologizes for any inconvenience this may cause. https://www.europeanreview.org/article/14464.
Insights
This study on MiR-16 and pituitary adenoma cell proliferation has been withdrawn due to suspected research misconduct. The publisher retracted the article as authors did not prove data originality.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Pituitary adenomas are common tumors affecting hormone regulation.
- MicroRNAs (miRNAs) play roles in tumor development.
- The ERK/MAPK pathway is implicated in cell proliferation.
Purpose of the Study:
- To investigate the role of MiR-16 in pituitary adenoma cell proliferation.
- To explore the potential involvement of the ERK/MAPK signaling pathway.
Main Methods:
- The study aimed to analyze MiR-16 expression in pituitary adenoma cells.
- Investigated the effect of MiR-16 on cell proliferation.
- Examined the impact on the ERK/MAPK signaling pathway.
Main Results:
- The article reported that MiR-16 inhibited pituitary adenoma cell proliferation.
- The proposed mechanism involved the suppression of the ERK/MAPK signal pathway.
Conclusions:
- The findings suggested MiR-16 as a potential therapeutic target.
- MiR-16's role in suppressing the ERK/MAPK pathway was highlighted.
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