<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>33(2)</volume><submitter>Nakano A</submitter><pubmed_abstract>Pancreatic neuroendocrine tumors (PanNETs) represent a rare subset of pancreatic cancers, comprising approximately 1-2% of all cases. Non-functioning PanNETs (NF-PanNETs), which account for the majority of PanNETs, can be difficult to treat as they show no hormone-related symptoms and are often not diagnosed until more advanced stages. Current therapeutic agents have limited efficacy, highlighting the need for novel treatment strategies. Multiple endocrine neoplasia type 1 is a hereditary syndrome strongly associated with PanNETs and pituitary neuroendocrine tumors (PitNETs), caused by germline mutations in the MEN1 gene. Using Men1 f/f-RipCre+ mice, which develop both NF-PanNETs and PitNETs, we investigated whether long-term administration of metformin, a first-line anti-diabetic drug, co</pubmed_abstract><journal>Endocrine-related cancer</journal><pagination>e250518</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12920065</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Metformin suppresses MEN1-associated pancreatic and pituitary neuroendocrine tumors: evidence from mouse models and clinical data.</pubmed_title><pmcid>PMC12920065</pmcid><pubmed_authors>Moro T</pubmed_authors><pubmed_authors>Terada K</pubmed_authors><pubmed_authors>Tajima T</pubmed_authors><pubmed_authors>Ishiai M</pubmed_authors><pubmed_authors>Hoshino C</pubmed_authors><pubmed_authors>Nakano A</pubmed_authors><pubmed_authors>Shirai R</pubmed_authors><pubmed_authors>Hijioka S</pubmed_authors><pubmed_authors>Kassai H</pubmed_authors><pubmed_authors>Ohki R</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Mistui Y</pubmed_authors><pubmed_authors>Tabata Y</pubmed_authors><pubmed_authors>Sakaguchi Y</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Yokoyama A</pubmed_authors><pubmed_authors>Sakata N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metformin suppresses MEN1-associated pancreatic and pituitary neuroendocrine tumors: evidence from mouse models and clinical data.</name><description>Pancreatic neuroendocrine tumors (PanNETs) represent a rare subset of pancreatic cancers, comprising approximately 1-2% of all cases. Non-functioning PanNETs (NF-PanNETs), which account for the majority of PanNETs, can be difficult to treat as they show no hormone-related symptoms and are often not diagnosed until more advanced stages. Current therapeutic agents have limited efficacy, highlighting the need for novel treatment strategies. Multiple endocrine neoplasia type 1 is a hereditary syndrome strongly associated with PanNETs and pituitary neuroendocrine tumors (PitNETs), caused by germline mutations in the MEN1 gene. Using Men1 f/f-RipCre+ mice, which develop both NF-PanNETs and PitNETs, we investigated whether long-term administration of metformin, a first-line anti-diabetic drug, co</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Feb</publication><modification>2026-07-16T12:59:56.982Z</modification><creation>2026-07-09T10:57:04.384Z</creation></dates><accession>S-EPMC12920065</accession><cross_references><pubmed>41568565</pubmed><doi>10.1530/ERC-25-0518</doi></cross_references></HashMap>