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PMID: 12580928 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Expression of pituitary tumour transforming gene (PTTG) and fibroblast growth factor-2 (FGF-2) in human pituitary adenomas: relationships to clinical tumour behaviour.

Clinical endocrinology ·Vol. 58 ·No. 2 ·2003-02-00 ·Pages 141-50

McCabe CJ, Khaira JS, Boelaert K, Heaney AP, Tannahill LA, Hussain S, Mitchell R, Olliff J, Sheppard MC, Franklyn JA, Gittoes NJ

Abstract

Pituitary tumour transforming gene (PTTG) encodes a multifunctional protein that is implicated in initiating and perpetuating pituitary adenoma growth. PTTG appears to have key regulatory functions in determining control of many fundamental cellular events including mitosis, cell transformation, DNA repair and gene regulation. Several of these events are mediated through interactions with PTTG binding factor (PBF) and fibroblast growth factor-2 (FGF-2). Given this background, we have determined the expression of PTTG, PBF, FGF-2 and its receptor FGF-R-1 in a large cohort of pituitary adenomas and have sought associations between levels of gene expression and clinical markers of tumour behaviour. We used real-time reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blot analyses to measure PTTG, PBF, FGF-2 and FGF-R-1 expression in ex vivo pituitary tumours (N = 121). Clinical data, including accurate radiological assessment of tumour characteristics, were used to determine any associations between gene expression and tumour behaviour. PTTG was increased significantly (fivefold, P = 0.005) in adenomas compared with normal pituitaries. We also demonstrated that PBF was similarly raised in adenomas (sixfold, P = 0.0001), and was significantly correlated with PTTG expression. FGF-2 and its receptor FGF-R-1 were also raised in adenomas compared with normal pituitary tissue. Moreover, significantly enhanced expression of FGF-R-1 was observed in invasive adenomas compared with other pituitary tumours. Our data support a fundamental role for PTTG-mediated upregulation of FGF-2 signalling in pituitary tumorigenesis and growth, and suggest that receptor-mediated mechanisms of growth factor action may be critically important. Further prospective studies are required to determine whether measurement of FGF-R-1 mRNA will be of clinical use as a prognostic marker in patients with pituitary adenomas.

MeSH Terms
Adenoma/chemistry,pathology Adult Biomarkers, Tumor/analysis Blotting, Western/methods Chi-Square Distribution Cohort Studies DNA-Binding Proteins/analysis,genetics Female Fibroblast Growth Factor 2/analysis,genetics Gene Expression Humans Intracellular Signaling Peptides and Proteins Magnetic Resonance Imaging Male Membrane Proteins Middle Aged Neoplasm Proteins/analysis,genetics Pituitary Neoplasms/chemistry,pathology RNA, Messenger/analysis Receptor Protein-Tyrosine Kinases/analysis,genetics Receptor, Fibroblast Growth Factor, Type 1 Receptors, Fibroblast Growth Factor/analysis,genetics Reverse Transcriptase Polymerase Chain Reaction Securin Statistics, Nonparametric
Chemicals
Biomarkers, Tumor DNA-Binding Proteins Intracellular Signaling Peptides and Proteins Membrane Proteins Neoplasm Proteins PTTG1IP protein, human RNA, Messenger Receptors, Fibroblast Growth Factor Securin pituitary tumor-transforming protein 1, human Fibroblast Growth Factor 2 FGFR1 protein, human Receptor Protein-Tyrosine Kinases Receptor, Fibroblast Growth Factor, Type 1
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
McCabe C J
Division of Medical Sciences, University of Birmingham, Queen Elizabeth Hospital, Edgbaston, Birmingham, UK. mccabcjz@bham.ac.uk
Khaira J S
Boelaert K
Heaney A P
Tannahill L A
Hussain S
Mitchell R
Olliff J
Sheppard M C
Franklyn J A
Gittoes N J L
Article Info
Journal
Clinical endocrinology
Abbr.
Clin Endocrinol (Oxf)
ISSN
0300-0664
Published
2003-02-00
Pages
141-50
Language
English
Region
England
NLM ID
0346653
Subset
IM
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