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Two-dimensional Gel Electrophoresis Coupled with Mass Spectrometry Methods for an Analysis of Human Pituitary Adenoma Tissue Proteome
Published on: April 2, 2018
Gene expression profiling in human null cell pituitary adenoma tissue.
Ji Hu1, Huaidong Song, Xuanchun Wang
1State Key Laboratory of Genetics Engineering, Institute of Endocrinology and Diabetology, Department of Endocrinology, Huashan Hospital, FuDan University, Shanghai 200040, PR China.
Researchers identified 17 differentially expressed genes in null cell pituitary tumors, including overexpressed synaptotagmin (SYT), ATP5B, and MDH1, offering insights into tumor development.
Area of Science:
- Endocrinology
- Molecular Biology
- Oncology
Background:
- Pituitary gland tumors, specifically null cell adenomas, are common but their development mechanisms are largely unknown.
- Understanding the genetic basis of these tumors is crucial for diagnosis and treatment.
Purpose of the Study:
- To investigate gene expression differences between null cell adenomas and normal pituitary tissue.
- To identify key genes involved in the pathogenesis of null cell pituitary adenomas.
Main Methods:
- Expressed sequence tags (EST) sequencing and cDNA microarray analysis were employed for large-scale gene expression profiling.
- RT-real-time quantitative PCR was used to validate the expression of selected genes.
Main Results:
- 17 genes were found to be differentially expressed in null cell adenomas compared to normal pituitary tissue.
- 14 genes were overexpressed, and 3 were underpressed.
- Overexpression of Synaptotagmin (SYT), ATP5B, and MDH1 was confirmed, suggesting potential roles in tumor function and energy metabolism.
Conclusions:
- The identified differentially expressed genes, particularly SYT, ATP5B, and MDH1, provide new insights into the oncogenesis of null cell pituitary adenomas.
- Overexpression of SYT may indicate potential for unknown hormone or peptide secretion.
- These findings contribute to a better understanding of null cell adenoma formation and development.
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