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Updated: Jan 29, 2026

Three-dimensional Alginate-bead Culture of Human Pituitary Adenoma Cells
Published on: February 18, 2016
Analysis of pituitary adenoma expression patterns suggests a potential role for the NeuroD1 transcription factor in
Lubov Borisovna Mitrofanova1, Olga Mikhailovna Vorobeva1, Andrey Nikolaevich Gorshkov1,2
1Almazov National Medical Research Center, St. Petersburg, Russia.
Abstract:
NeuroD1's roles in the pathogenesis of pituitary adenomas and in the biology of the normal adult pituitary gland have been insufficiently researched. Much of the work investigating its expression patterns has yielded contradictory results.
Objective:
morphological study of NeuroD1 transcription factor expression in different types of pituitary adenomas and in normal adult human pituitary glands.
Materials And Methods:
This study analyzed 48 pituitary adenomas and nine normal pituitary glands. In all cases, immunohistochemical study was performed with antibodies to NeuroD1, 6 hormones of adenohypophysis, Ki-67, and CK7. We used confocal laser scanning microscopy, electron microscopy and electron immunocytochemistry.
Results:
NeuroD1 expression was detected in all cases of plurihormonal adenomas, mammosomatotropinomas, corticotropinomas, prolactinomas, gonadotropinomas, null-cell pituitary adenomas, and in normal pituitary glands. The average numbers of NeuroD1 expressing cells in normal adenohypophysis specimens were significantly lower than in the adenomas overall (p=0.006). NeuroD1 expression was confirmed by several methods (in prolactinomas, by double stain immunohistochemistry; in mammosomatotropinomas, by double stain immunohistochemistry, confocal laser scanning microscopy, and electron immunocytochemistry; and in somatotropinomas, by electron immunocytochemistry).
Conclusion:
Immunohistochemistry, confocal microscopy, and double label electron immunocytochemistry confirmed NeuroD1's key role in the pathogenesis of pituitary tumors, regardless of their hormonal state. Its expression level in pituitary adenomas is significantly higher than in the normal pituitary gland and has no reliable correlation with any studied hormones or Ki-67. These findings suggest that NeuroD1 should be investigated further as a potential molecular target in tumor-targeting therapies.
Insights
NeuroD1 (Neurogenic differentiation 1) is highly expressed in pituitary tumors compared to normal glands. This suggests NeuroD1 is crucial in pituitary adenoma development and a potential target for new therapies.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- The role of NeuroD1 in pituitary adenoma pathogenesis is not well understood.
- Previous studies on NeuroD1 expression patterns in the pituitary have yielded conflicting results.
Purpose of the Study:
- To investigate the expression patterns of the NeuroD1 transcription factor in various pituitary adenomas and normal adult human pituitary glands.
- To clarify NeuroD1's role in the biology of the normal pituitary and in the development of pituitary tumors.
Main Methods:
- Immunohistochemistry was performed on 48 pituitary adenomas and 9 normal pituitary glands.
- Antibodies against NeuroD1, 6 adenohypophyseal hormones, Ki-67, and CK7 were used.
- Confocal laser scanning microscopy, electron microscopy, and electron immunocytochemistry were employed for detailed analysis.
Main Results:
- NeuroD1 expression was detected in all analyzed pituitary adenoma types and normal pituitary glands.
- The average number of NeuroD1-expressing cells was significantly higher in pituitary adenomas than in normal pituitary tissue (p=0.006).
- NeuroD1 expression was confirmed across multiple methods in specific tumor types, validating its presence.
Conclusions:
- NeuroD1 plays a significant role in the pathogenesis of pituitary tumors, irrespective of their hormonal classification.
- Pituitary adenomas exhibit significantly higher NeuroD1 expression levels compared to normal pituitary glands.
- NeuroD1 expression did not correlate reliably with studied hormones or Ki-67, indicating its potential as a distinct therapeutic target.
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