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Nuclear exclusion of menin drives functional MEN1 deficiency in non-MEN1 prolactinomas: mouse models and human biopsies

2026-08-24

Abstract excerpt

<h4>ABSTRACT</h4> Prolactinomas, the most common secretory pituitary tumour subtype, frequently occur in patients with Multiple Endocrine Neoplasia type 1, caused by germline MEN1 mutations encoding menin. While menin loss is well established in MEN1-associated prolactinomas, its role in sporadic tumours remains unclear. We investigated menin expression, subcellular localization, and downstream signalling in two...

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Literature Corpus work
a1795913-a3f4-5e39-b947-9b25310619bc
DOI
10.64898/2026.08.19.745771
Open publication

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Nuclear exclusion of menin drives functional MEN1 deficiency in non-MEN1 prolactinomas: mouse models and human biopsiesDOI 10.64898/2026.08.19.745771
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