<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>59(6)</volume><submitter>Grouwels G</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>Generating functional beta-cells by inducing their proliferation may provide new perspectives for cell therapy in diabetes. Transcription factor E2F1 controls G(1)- to S-phase transition during the cycling of many cell types and is required for pancreatic beta-cell growth and function. However, the consequences of overexpression of E2F1 in beta-cells are unknown.&lt;h4>Research design and methods&lt;/h4>The effects of E2F1 overexpression on beta-cell proliferation and function were analyzed in isolated rat beta-cells and in transgenic mice.&lt;h4>Results&lt;/h4>Adenovirus AdE2F1-mediated overexpression of E2F1 increased the proliferation of isolated primary rat beta-cells 20-fold but also enhanced beta-cell death. Coinfection with adenovirus AdAkt expressing a constitutively active f</pubmed_abstract><journal>Diabetes</journal><pagination>1435-44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2874704</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Ectopic expression of E2F1 stimulates beta-cell proliferation and function.</pubmed_title><pmcid>PMC2874704</pmcid><pubmed_authors>Leuckx G</pubmed_authors><pubmed_authors>Hoebeke I</pubmed_authors><pubmed_authors>Chintinne M</pubmed_authors><pubmed_authors>Heimberg H</pubmed_authors><pubmed_authors>Cai Y</pubmed_authors><pubmed_authors>Ziebold U</pubmed_authors><pubmed_authors>Van de Casteele M</pubmed_authors><pubmed_authors>Grouwels G</pubmed_authors><pubmed_authors>Stange G</pubmed_authors><pubmed_authors>Ling Z</pubmed_authors><pubmed_authors>Pipeleers D</pubmed_authors><pubmed_authors>Heremans Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ectopic expression of E2F1 stimulates beta-cell proliferation and function.</name><description>&lt;h4>Objective&lt;/h4>Generating functional beta-cells by inducing their proliferation may provide new perspectives for cell therapy in diabetes. Transcription factor E2F1 controls G(1)- to S-phase transition during the cycling of many cell types and is required for pancreatic beta-cell growth and function. However, the consequences of overexpression of E2F1 in beta-cells are unknown.&lt;h4>Research design and methods&lt;/h4>The effects of E2F1 overexpression on beta-cell proliferation and function were analyzed in isolated rat beta-cells and in transgenic mice.&lt;h4>Results&lt;/h4>Adenovirus AdE2F1-mediated overexpression of E2F1 increased the proliferation of isolated primary rat beta-cells 20-fold but also enhanced beta-cell death. Coinfection with adenovirus AdAkt expressing a constitutively active f</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Jun</publication><modification>2025-04-26T06:20:02.583Z</modification><creation>2019-03-27T00:30:58Z</creation></dates><accession>S-EPMC2874704</accession><cross_references><pubmed>20299467</pubmed><doi>10.2337/db09-1295</doi></cross_references></HashMap>