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Published in: Pituitary 1/2014

01-02-2014

Increased serum interleukin-22 levels in patients with PRL-secreting and non-functioning pituitary macroadenomas

Authors: S. Cannavo, F. Ferrau, O. R. Cotta, S. Saitta, V. Barresi, M. T. Cristani, A. Saija, R. M. Ruggeri, F. Trimarchi, S. Gangemi

Published in: Pituitary | Issue 1/2014

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Abstract

Cytokines’ involvement in tumorigenesis has been hypothesized. Interleukin-22 (IL-22) is implicated in proliferative and anti-apoptotic pathways via its receptor IL-22R. Its role in pituitary adenomas has never been investigated. Twenty-seven patients with pituitary macroadenomas (PA, 21 males, mean age 53.8 ± 14.4 years) and 30 healthy controls (19 males, mean age 50.4 ± 8.4 years) were enrolled. Out of 27 PA patients, 17 had a non-functioning tumour (NFPA) and 10 a PRL-secreting adenoma (PRL-oma). Serum IL-22 levels were measured in both patients and controls. Immunohistochemical (IHC) tumoral IL-22R expression was evaluated in 10 patients with NFPA and 4 with PRL-oma. IL-22 levels were significantly higher in PA patients than in controls [32.47 (11.29–70.12) vs. 5.58 (0.19–21.46) pg/mL, p < 0.0001] but did not correlate with tumor maximum diameter and were not associated to pituitary function impairment. PRL-oma patients had significantly higher IL-22 levels than NFPA patients [37.18 (14.82–70.12) vs. 21.29 (11.29–56) pg/mL, p = 0.039]. IHC revealed a strong IL-22R staining in 100 % of PRL-omas and 60 % of NFPAs. We provide the first evidence of increased serum IL-22 levels in patients with pituitary macroadenoma, especially in PRL-omas, regardless of tumor size and/or degree of pituitary function impairment. We also demonstrated the expression of IL22R in all PRL-omas and in 60 % of NFPAs.
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Metadata
Title
Increased serum interleukin-22 levels in patients with PRL-secreting and non-functioning pituitary macroadenomas
Authors
S. Cannavo
F. Ferrau
O. R. Cotta
S. Saitta
V. Barresi
M. T. Cristani
A. Saija
R. M. Ruggeri
F. Trimarchi
S. Gangemi
Publication date
01-02-2014
Publisher
Springer US
Published in
Pituitary / Issue 1/2014
Print ISSN: 1386-341X
Electronic ISSN: 1573-7403
DOI
https://doi.org/10.1007/s11102-013-0468-2

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