Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data

Pituitary adenomas, monoclonal in origin, are the most common intracranial neoplasms. Altered gene expression as well as somatic mutations is detected frequently in pituitary adenomas. The purpose of this study was to detect differentially expressed genes (DEGs) and biological processes during tumor...

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Main Authors: Peng Zhao, Wei Hu, Hongyun Wang, Shengyuan Yu, Chuzhong Li, Jiwei Bai, Songbai Gui, Yazhuo Zhang
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2015/164087
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author Peng Zhao
Wei Hu
Hongyun Wang
Shengyuan Yu
Chuzhong Li
Jiwei Bai
Songbai Gui
Yazhuo Zhang
author_facet Peng Zhao
Wei Hu
Hongyun Wang
Shengyuan Yu
Chuzhong Li
Jiwei Bai
Songbai Gui
Yazhuo Zhang
author_sort Peng Zhao
collection DOAJ
description Pituitary adenomas, monoclonal in origin, are the most common intracranial neoplasms. Altered gene expression as well as somatic mutations is detected frequently in pituitary adenomas. The purpose of this study was to detect differentially expressed genes (DEGs) and biological processes during tumor formation of pituitary adenomas. We performed an integrated analysis of publicly available GEO datasets of pituitary adenomas to identify DEGs between pituitary adenomas and normal control (NC) tissues. Gene function analysis including Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and protein-protein interaction (PPI) networks analysis was conducted to interpret the biological role of those DEGs. In this study we detected 3994 DEGs (2043 upregulated and 1951 downregulated) in pituitary adenoma through an integrated analysis of 5 different microarray datasets. Gene function analysis revealed that the functions of those DEGs were highly correlated with the development of pituitary adenoma. This integrated analysis of microarray data identified some genes and pathways associated with pituitary adenoma, which may help to understand the pathology underlying pituitary adenoma and contribute to the successful identification of therapeutic targets for pituitary adenoma.
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institution Kabale University
issn 1687-8337
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language English
publishDate 2015-01-01
publisher Wiley
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series International Journal of Endocrinology
spelling doaj-art-0c1f3e64b5c847219a6d8a1c5b968c7f2025-02-03T01:22:38ZengWileyInternational Journal of Endocrinology1687-83371687-83452015-01-01201510.1155/2015/164087164087Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray DataPeng Zhao0Wei Hu1Hongyun Wang2Shengyuan Yu3Chuzhong Li4Jiwei Bai5Songbai Gui6Yazhuo Zhang7Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaDepartment of Cardiology, Beijing Chuiyangliu Hospital, Beijing, ChinaBeijing Neurosurgical Institute, Center of Brain Tumor, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, ChinaBeijing Neurosurgical Institute, Center of Brain Tumor, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, ChinaBeijing Neurosurgical Institute, Center of Brain Tumor, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, ChinaDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaDepartment of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, ChinaBeijing Neurosurgical Institute, Center of Brain Tumor, Beijing Institute for Brain Disorders, Capital Medical University, Beijing, ChinaPituitary adenomas, monoclonal in origin, are the most common intracranial neoplasms. Altered gene expression as well as somatic mutations is detected frequently in pituitary adenomas. The purpose of this study was to detect differentially expressed genes (DEGs) and biological processes during tumor formation of pituitary adenomas. We performed an integrated analysis of publicly available GEO datasets of pituitary adenomas to identify DEGs between pituitary adenomas and normal control (NC) tissues. Gene function analysis including Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis, and protein-protein interaction (PPI) networks analysis was conducted to interpret the biological role of those DEGs. In this study we detected 3994 DEGs (2043 upregulated and 1951 downregulated) in pituitary adenoma through an integrated analysis of 5 different microarray datasets. Gene function analysis revealed that the functions of those DEGs were highly correlated with the development of pituitary adenoma. This integrated analysis of microarray data identified some genes and pathways associated with pituitary adenoma, which may help to understand the pathology underlying pituitary adenoma and contribute to the successful identification of therapeutic targets for pituitary adenoma.http://dx.doi.org/10.1155/2015/164087
spellingShingle Peng Zhao
Wei Hu
Hongyun Wang
Shengyuan Yu
Chuzhong Li
Jiwei Bai
Songbai Gui
Yazhuo Zhang
Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data
International Journal of Endocrinology
title Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data
title_full Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data
title_fullStr Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data
title_full_unstemmed Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data
title_short Identification of Differentially Expressed Genes in Pituitary Adenomas by Integrating Analysis of Microarray Data
title_sort identification of differentially expressed genes in pituitary adenomas by integrating analysis of microarray data
url http://dx.doi.org/10.1155/2015/164087
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