Differential gene expression in pituitary adenomas by oligonucleotide array analysis.

OBJECTIVES: Microarray technology allows for the expression profile of many thousands of genes to be quantified at the same time, and has resulted in novel discoveries about the tumour biology of a number of cancers. We sought to do this in pituitary adenomas, the most common intracranial neoplasm....

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Main Authors: Morris, D, Musat, M, Czirják, S, Hanzély, Z, Lillington, D, Korbonits, M, Grossman, AB
Format: Journal article
Language:English
Published: 2005
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author Morris, D
Musat, M
Czirják, S
Hanzély, Z
Lillington, D
Korbonits, M
Grossman, AB
author_facet Morris, D
Musat, M
Czirják, S
Hanzély, Z
Lillington, D
Korbonits, M
Grossman, AB
author_sort Morris, D
collection OXFORD
description OBJECTIVES: Microarray technology allows for the expression profile of many thousands of genes to be quantified at the same time, and has resulted in novel discoveries about the tumour biology of a number of cancers. We sought to do this in pituitary adenomas, the most common intracranial neoplasm. METHODS: Affymetrix GeneChip HG-U133A oligonucleotide arrays covering 14 500 well-characterised genes from the human genome were used to study pooled RNA for each of the four major pituitary adenoma subtypes. Individual gene-expression levels in the tumours were compared relative to the expression profile in normal pooled pituitary RNA. Three differentially expressed genes with potential importance in tumourigenesis were chosen for validation by real-time quantitative PCR on the original tumours and on an additional 26 adenomas. RESULTS: Bioinformatic analysis showed that 3906 genes and 351 expressed sequence tags were differentially expressed among all pituitary tumour subtypes. Lysosomal-associated protein transmembrane- 4-beta (LAPTM4B), a novel gene upregulated in hepatocellular carcinoma, was significantly over-expressed in adrenocorticotrophin (ACTH)-secreting adenomas and non-functioning pituitary adenomas (NFPAs). Bcl-2-associated athanogene (BAG1), an anti-apoptotic protein found at high levels in a number of human cancers, was significantly over-expressed in growth hormone-secreting and prolactin-secreting adenomas and NFPAs. The cyclin-dependent kinase inhibitor p18, in which murine gene deletion has been shown to produce pituitary ACTH cell hyperplasia and adenomas, was significantly under-expressed in ACTH-secreting adenomas. CONCLUSIONS: Expression array analysis of pituitary adenomas using the Affymetrix GeneChip HG-U133A arrays appears to be a valid method of identifying genes that may be important in tumour pathogenesis.
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spelling oxford-uuid:36dda830-90ed-4fab-bc13-ad2c1bac02202022-03-26T13:40:33ZDifferential gene expression in pituitary adenomas by oligonucleotide array analysis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:36dda830-90ed-4fab-bc13-ad2c1bac0220EnglishSymplectic Elements at Oxford2005Morris, DMusat, MCzirják, SHanzély, ZLillington, DKorbonits, MGrossman, AB OBJECTIVES: Microarray technology allows for the expression profile of many thousands of genes to be quantified at the same time, and has resulted in novel discoveries about the tumour biology of a number of cancers. We sought to do this in pituitary adenomas, the most common intracranial neoplasm. METHODS: Affymetrix GeneChip HG-U133A oligonucleotide arrays covering 14 500 well-characterised genes from the human genome were used to study pooled RNA for each of the four major pituitary adenoma subtypes. Individual gene-expression levels in the tumours were compared relative to the expression profile in normal pooled pituitary RNA. Three differentially expressed genes with potential importance in tumourigenesis were chosen for validation by real-time quantitative PCR on the original tumours and on an additional 26 adenomas. RESULTS: Bioinformatic analysis showed that 3906 genes and 351 expressed sequence tags were differentially expressed among all pituitary tumour subtypes. Lysosomal-associated protein transmembrane- 4-beta (LAPTM4B), a novel gene upregulated in hepatocellular carcinoma, was significantly over-expressed in adrenocorticotrophin (ACTH)-secreting adenomas and non-functioning pituitary adenomas (NFPAs). Bcl-2-associated athanogene (BAG1), an anti-apoptotic protein found at high levels in a number of human cancers, was significantly over-expressed in growth hormone-secreting and prolactin-secreting adenomas and NFPAs. The cyclin-dependent kinase inhibitor p18, in which murine gene deletion has been shown to produce pituitary ACTH cell hyperplasia and adenomas, was significantly under-expressed in ACTH-secreting adenomas. CONCLUSIONS: Expression array analysis of pituitary adenomas using the Affymetrix GeneChip HG-U133A arrays appears to be a valid method of identifying genes that may be important in tumour pathogenesis.
spellingShingle Morris, D
Musat, M
Czirják, S
Hanzély, Z
Lillington, D
Korbonits, M
Grossman, AB
Differential gene expression in pituitary adenomas by oligonucleotide array analysis.
title Differential gene expression in pituitary adenomas by oligonucleotide array analysis.
title_full Differential gene expression in pituitary adenomas by oligonucleotide array analysis.
title_fullStr Differential gene expression in pituitary adenomas by oligonucleotide array analysis.
title_full_unstemmed Differential gene expression in pituitary adenomas by oligonucleotide array analysis.
title_short Differential gene expression in pituitary adenomas by oligonucleotide array analysis.
title_sort differential gene expression in pituitary adenomas by oligonucleotide array analysis
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AT czirjaks differentialgeneexpressioninpituitaryadenomasbyoligonucleotidearrayanalysis
AT hanzelyz differentialgeneexpressioninpituitaryadenomasbyoligonucleotidearrayanalysis
AT lillingtond differentialgeneexpressioninpituitaryadenomasbyoligonucleotidearrayanalysis
AT korbonitsm differentialgeneexpressioninpituitaryadenomasbyoligonucleotidearrayanalysis
AT grossmanab differentialgeneexpressioninpituitaryadenomasbyoligonucleotidearrayanalysis