Multiple Endocrine Neoplasia I (MEN1) - Синдром Вермера

MEN1 is a putative tumor suppressor associated with multiple endocrine neoplasia type 1. In vitro studies have shown that menin is localized to the nucleus, possesses two functional nuclear localization signals, and inhibits transcriptional activation by JunD, however, the function of this protein is not known. Two messages have been detected on northern blots but the larger message has not been characterized. Two variants of the shorter transcript have been identified where alternative splicing affects the coding sequence. Five variants where alternative splicing takes place in the 5""" UTR have also been identified.Prognosis in MEN1 patients is related to hormonal hypersecretion by tumors, such as hypergastrinemia causing severe peptic ulcer disease, primary hyperparathyroidism, and acute forms of hyperinsulinemia.