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The role of E and N-cadherin in the postoperative course of gonadotroph pituitary tumours.

Authors :
Øystese KAB
Berg JP
Normann KR
Zucknick M
Casar-Borota O
Bollerslev J
Source :
Endocrine [Endocrine] 2018 Nov; Vol. 62 (2), pp. 351-360. Date of Electronic Publication: 2018 Jul 26.
Publication Year :
2018

Abstract

Purpose: Gonadotroph tumours are the most abundant of the clinically silent pituitary tumours. There is a lack of reliable prognostic markers predicting their clinical course. Our aim was to determine the level of E-cadherin and N-cadherin in a cohort of clinically silent gonadotroph pituitary tumours, and compare them to the rate of reintervention.<br />Methods: Tumour tissue from primary surgery was retrospectively investigated and compared with clinical data. Immunohistochemical (N = 105) and real time-qPCR (N = 85) analyses for the levels of N-cadherin and the extra- and intracellular domains of E-cadherin were performed. The immunoreactive scores (IRS) and mRNA relative quantity were compared to the rate of reintervention.<br />Results: The tumours presented a high IRS for N-cadherin (Median 12 (IQR 12-12)) and almost no immunoreactivity for the extracellular domain of E-cadherin (Median 0 (IQR 0-0)). The membranous staining for the intracellular domain of E-cadherin varied (Median 6 (IQR 4-6). Reduced membranous expression of the intracellular domain of E-cadherin was associated with nuclear presence of the same domain. Nuclear staining for the intracellular domain of E-cadherin was associated with a lower rate of reintervention (p = 0.01).<br />Conclusion: We found that silent gonadotroph tumours presented high IRS for N-cadherin and low IRS for the extracellular domain of E-cadherin. A substantial proportion of the tumours presented nuclear staining for the intracellular domain of E-cadherin, accompanied by a reduced membranous expression of the intracellular domain of E-cadherin. Absence of nuclear staining for the intracellular domain of E-cadherin served as an independent predictor of reintervention.

Details

Language :
English
ISSN :
1559-0100
Volume :
62
Issue :
2
Database :
MEDLINE
Journal :
Endocrine
Publication Type :
Academic Journal
Accession number :
30051197
Full Text :
https://doi.org/10.1007/s12020-018-1679-0