Alternative Lengthening of Telomeres and Differential Expression of Endocrine Transcription Factors Distinguish Metastatic and Non-metastatic Insulinomas

Insulin-producing pancreatic neuroendocrine tumors (PanNETs)/insulinomas are generally considered to be indolent tumors with an excellent prognosis after complete resection. However, some insulinomas have a poor prognosis due to relapses and metastatic disease. Recently, studies in non-functional Pa...

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Veröffentlicht in:Endocrine pathology 2020-06, Vol.31 (2), p.108-118
Hauptverfasser: Hackeng, Wenzel M., Schelhaas, Willemien, Morsink, Folkert H. M., Heidsma, Charlotte M., van Eeden, Susanne, Valk, Gerlof D., Vriens, Menno R., Heaphy, Christopher M., Nieveen van Dijkum, Els J. M., Offerhaus, G. Johan A., Dreijerink, Koen M. A., Brosens, Lodewijk A. A.
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Sprache:eng
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Zusammenfassung:Insulin-producing pancreatic neuroendocrine tumors (PanNETs)/insulinomas are generally considered to be indolent tumors with an excellent prognosis after complete resection. However, some insulinomas have a poor prognosis due to relapses and metastatic disease. Recently, studies in non-functional PanNETs indicated that behavior can be stratified according to alpha- and beta-cell differentiation, as defined by expression of the transcription factors ARX and PDX1, respectively. It is unknown whether similar mechanisms play a role in insulinomas. Therefore, we determined ARX and PDX1 expression in a cohort of 35 sporadic primary insulinomas and two liver metastases of inoperable primary insulinomas. In addition, WHO grade and loss of ATRX or DAXX were determined by immunohistochemistry, and alternative lengthening of telomeres (ALT) and CDKN2A status by fluorescence in situ hybridization. These findings were correlated with tumor characteristics and clinical follow-up data. In total, five out of 37 insulinoma patients developed metastatic disease. Metastatic insulinomas were all larger than 3 cm, whereas the indolent insulinomas were smaller ( p value
ISSN:1046-3976
1559-0097
DOI:10.1007/s12022-020-09611-8