<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Zhao S</submitter><funding>Beijing Municipal Science and Technology Commission</funding><funding>National Natural Science Foundation of China</funding><pubmed_abstract>The 14-3-3 protein family has attracted much attention in research into the pathogenesis of human tumors because of its involvement in tumorigenesis. In previous studies, we found that 14-3-3η was highly expressed in pituitary oncocytoma. However, the mechanism by which 14-3-3η regulates tumorigenesis in pituitary oncocytoma is unclear. 14-3-3η-binding proteins were investigated in pituitary oncocytoma by immunoprecipitation and proteomic analysis. A total of 443 proteins were identified as 14-3-3η binding proteins. The interactions of 14-3-3η and its binding partners were identified by a network analysis using the STRING database. The network included 433 nodes and 564 edges. PRAS40 (AKT1S1) was a binding protein of 14-3-3η and showed experimental interactions with 14-3-3η in the STRING d</pubmed_abstract><journal>Frontiers in endocrinology</journal><pagination>797</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6893364</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The Apoptosis Regulator 14-3-3η and Its Potential as a Therapeutic Target in Pituitary Oncocytoma.</pubmed_title><pmcid>PMC6893364</pmcid><pubmed_authors>Zhao S</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Feng J</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Miao Y</pubmed_authors><pubmed_authors>Gong L</pubmed_authors><pubmed_authors>Li B</pubmed_authors><pubmed_authors>Gao H</pubmed_authors><pubmed_authors>Wang H</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Apoptosis Regulator 14-3-3η and Its Potential as a Therapeutic Target in Pituitary Oncocytoma.</name><description>The 14-3-3 protein family has attracted much attention in research into the pathogenesis of human tumors because of its involvement in tumorigenesis. In previous studies, we found that 14-3-3η was highly expressed in pituitary oncocytoma. However, the mechanism by which 14-3-3η regulates tumorigenesis in pituitary oncocytoma is unclear. 14-3-3η-binding proteins were investigated in pituitary oncocytoma by immunoprecipitation and proteomic analysis. A total of 443 proteins were identified as 14-3-3η binding proteins. The interactions of 14-3-3η and its binding partners were identified by a network analysis using the STRING database. The network included 433 nodes and 564 edges. PRAS40 (AKT1S1) was a binding protein of 14-3-3η and showed experimental interactions with 14-3-3η in the STRING d</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-05-04T01:04:03.516Z</modification><creation>2020-05-22T00:01:43Z</creation></dates><accession>S-EPMC6893364</accession><cross_references><pubmed>31849836</pubmed><doi>10.3389/fendo.2019.00797</doi></cross_references></HashMap>