Reduced Levels of E-cadherin Correlate with Progression of Corticotroph Pituitary Tumours
Overview
Authors
Affiliations
Objectives: Loss of E-cadherin is an important marker of epithelial tumour progression. The aims of this study were to explore whether E-cadherin expression and localization correlate to corticotroph tumour progression, relate the expression of the E-cadherin gene (CDH1) to immunohistochemical E-cadherin staining pattern, and study whether the E-cadherin levels were correlated to methylation status of the CDH1 promoter region.
Design: Immunohistochemical analyses of E-cadherin protein were performed, as was RT-qPCR of the CDH1 and the POMC genes. Methylation pattern of the promoter region of CDH1 was measured using pyrosequencing of bisulfite-treated DNA.
Patients: Forty-five patients operated at a tertiary referral centre in Oslo, Norway. Adenoma tissue sections and RNA samples from patients with verified Cushing's disease or Nelson's syndrome were collected.
Measurements: Expression of E-cadherin mRNA and protein in pituitary corticotroph adenomas and average percentage of methylated cytosines in a cytosine-phosphate-guanosine island of the CDH1 promoter.
Results: Correlations were observed between tumour progression and both nuclear expression of E-cadherin and reduced CDH1 mRNA. The E-cadherin expression was not determined by the methylation pattern of the CDH1 promoter.
Conclusions: Corticotroph tumour progression was associated with reduced expression of the epithelial marker E-cadherin.
DNA Methylation in Pituitary Adenomas: A Scoping Review.
Moller M, Nortvig M, Andersen M, Poulsen F Int J Mol Sci. 2025; 26(2).
PMID: 39859246 PMC: 11765255. DOI: 10.3390/ijms26020531.
Xu D, Wang L, Zheng M Immun Inflamm Dis. 2024; 12(12):e70098.
PMID: 39688352 PMC: 11650491. DOI: 10.1002/iid3.70098.
Stem cell-associated transcription factors in non-functioning pituitary neuroendocrine tumours.
Oystese K, Olarescu N, Lindskog C, Xheka F, Berg-Johnsen J, Berg J Free Neuropathol. 2024; 5.
PMID: 38845811 PMC: 11155689. DOI: 10.17879/freeneuropathology-2024-5396.
Jotanovic J, Tebani A, Hekmati N, Sivertsson A, Lindskog C, Uhlen M J Endocr Soc. 2024; 8(5):bvae040.
PMID: 38505563 PMC: 10949357. DOI: 10.1210/jendso/bvae040.
Gil J, Marques-Pamies M, Valassi E, Garcia-Martinez A, Serra G, Hostalot C Biomedicines. 2022; 10(2).
PMID: 35203668 PMC: 8962441. DOI: 10.3390/biomedicines10020460.