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Published on: January 17, 2018
Study on miRNAs' Expression for the Invasion of Pituitary Adenomas
Guoqiang Yu1, Hongyun Wang, Shengyuan Yu
1Tsinghua University, Medical Center, Beijing, China.
Aim:
To explore the possible invasive effect of four microRNAs (miRNAs) in invasive pituitary adenomas.
Material And Methods:
Based on our previous studies, several in silico algorithms, and relative literature, 30 Han Chinese patients with invasive pituitary adenomas and 30 with non-invasive pituitary adenomas were involved in this research. The proteins related to invasion underwent immunohistochemical staining, including basic fibroblast growth factor (FGF2), pituitary tumor transforming gene (PTTG), cyclin B1 (CCNB1), survivin, focal adhesion kinase (FAK), and microvessel density (MVD). To validate the effect of miRNAs, miR-24, miR-93, miR-126, and miR-34a were chosen as possible targets for the aforementioned proteins with four in silico algorithms. All miRNAs tests were performed using quantitative real-time polymerase chain reaction (qPCR). The expression levels of proteins and miRNAs associated with tumors' invasiveness were analyzed.
Results:
In our study, FGF2, FAK, PTTG, CCNB1, and MVD were overexpressed in the invasive group compared with the noninvasive group, while an increase in the expression of survivin in the invasive group did not achieve statistical significance. This paper reviewed the literature, and four miRNAs involving invasion were selected for study: miR-24, miR-34a, miR-93, and miR-126. Under-expression of miR-24, miR-34a, and miR-93 was significant in the invasive group, while a decrease of miR-126 expression in the invasive group did not achieve statistical significance.
Conclusion:
FGF2, PTTG, CCNB1, survivin, FAK, and MVD proteins of pituitary adenoma showed strong expression in invasive tumors. Furthermore, miR-24, miR-93, miR-34a, and miR-126 were under-expressed in invasive Pituitary adenomas compared with non-invasive ones. The results indicated some relationship between the miRNA and protein expression during the pituitary invasion process.
Insights
Invasive pituitary adenomas show higher expression of FGF2, PTTG, CCNB1, FAK, and MVD proteins. Key microRNAs (miRNAs), including miR-24, miR-93, and miR-34a, were found to be under-expressed in invasive tumors.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Pituitary adenomas are common tumors, with invasive subtypes posing significant clinical challenges.
- Understanding the molecular mechanisms underlying pituitary adenoma invasion is crucial for developing targeted therapies.
Purpose of the Study:
- To investigate the role of specific microRNAs (miRNAs) in the invasive potential of pituitary adenomas.
- To correlate miRNA expression levels with key proteins involved in tumor invasion.
Main Methods:
- Comparative analysis of protein expression (FGF2, PTTG, CCNB1, survivin, FAK, MVD) in invasive versus non-invasive pituitary adenomas using immunohistochemistry.
- Quantitative real-time polymerase chain reaction (qPCR) to assess the expression of miR-24, miR-93, miR-126, and miR-34a.
- In silico analysis to identify potential miRNA-protein interactions.
Main Results:
- Proteins FGF2, FAK, PTTG, CCNB1, and MVD were significantly overexpressed in invasive pituitary adenomas compared to non-invasive ones.
- Under-expression of miR-24, miR-34a, and miR-93 was observed in the invasive group.
- miR-126 expression did not show a statistically significant difference between invasive and non-invasive groups.
Conclusions:
- Elevated expression of specific proteins (FGF2, PTTG, CCNB1, FAK, MVD) is associated with pituitary adenoma invasiveness.
- Downregulation of miR-24, miR-93, and miR-34a may contribute to the invasive phenotype of pituitary adenomas.
- A potential relationship exists between miRNA and protein expression patterns in pituitary adenoma invasion.
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