Article ID Journal Published Year Pages File Type
8476438 Molecular and Cellular Endocrinology 2018 30 Pages PDF
Abstract
The MEN1 gene encodes MENIN, a tumor suppressor that plays a role in multiple cellular processes. Germline and somatic mutations in MEN1 have been identified in hereditary and sporadic tumors of neuroendocrine origins suggesting context-specific functions. In this review, we focus on the development of mutational Men1 in vivo models, the known cellular activities of MENIN and efforts to identify vulnerabilities in tumors with MENIN loss.
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Life Sciences Biochemistry, Genetics and Molecular Biology Cell Biology
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