The EMT status in the primary tumor of adamantinomatous craniopharyngioma predict postoperative recurrence in children

Introduction Adamantinomatous craniopharyngiomas (ACP) are rare epithelial tumors, which by the WHO are classified as non-malignant tumors. Despite radical tumor regression, almost 57% of patients develop a craniopharyngioma recurrence. The pathogenesis of epithelial cancers involves a process calle...

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Veröffentlicht in:Child's nervous system 2025-12, Vol.41 (1), p.68, Article 68
Hauptverfasser: Bajdak-Rusinek, K., Diak, N., Gutmajster, E., Fus-Kujawa, A., Stępień, K. L., Wójtowicz, W., Kalina, M., Mandera, M.
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Sprache:eng
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Zusammenfassung:Introduction Adamantinomatous craniopharyngiomas (ACP) are rare epithelial tumors, which by the WHO are classified as non-malignant tumors. Despite radical tumor regression, almost 57% of patients develop a craniopharyngioma recurrence. The pathogenesis of epithelial cancers involves a process called epithelial-mesenchymal transition (EMT), which is involved in tumor progression and its invasion, and the loss of E-cadherin is crucial for this process. Undoubtedly, EMT also plays a role in the progression of ACP, but there are no studies that would examine its role in predicting postoperative tumor recurrence. Therefore, in our study, we aimed to compare the expression of EMT inducers and their markers, namely E-cadherin and vimentin, in material from two groups of pediatric patients, first with postoperative ACP relapse and second without relapse. Methods A total of 35 formalin-fixed, paraffin-embedded tissue blocks of pediatric patients (19 girls and 16 boys, from 2 to 17 years old) were included. The material was collected during craniopharyngioma resection in the years 2000–2019 and after then examined by the Department of Pathomorphology. Gene expression analysis was done using qRT-PCR. Results In the studied group of 35 patients, high levels of E-cad and low levels of vimentin expression were found in patients who did not experience relapse ( n  = 25, p  
ISSN:0256-7040
1433-0350
1433-0350
DOI:10.1007/s00381-024-06731-y