<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(10)</volume><submitter>You L</submitter><pubmed_abstract>Hyperglycemia is one of the possible causes for osteoporosis and bone fracture in diabetes mellitus. Here we modeled diabetes-induced osteoporosis in vitro using preosteoblastic cell line MC3T3-E1 and a diabetic mice model for in vivo studies. We found that in addition to reducing osteoblast viability and differentiation (mineralization), culture in elevated glucose down regulated microRNA-378 (miR-378) expression but ectopic miR-378 expression reversed the effects of high glucose. We identified caspase-3 (CASP3) as a target of miR-378 and showed that miR-378 repressed CASP3 mRNA and protein expression under high glucose condition. We further showed that both miR-378 expression and CASP3 silencing independently restored alkaline phosphatase (ALP) activity and the expression of osteoblastic</pubmed_abstract><journal>International journal of clinical and experimental pathology</journal><pagination>7249-61</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4230144</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MiR-378 overexpression attenuates high glucose-suppressed osteogenic differentiation through targeting CASP3 and activating PI3K/Akt signaling pathway.</pubmed_title><pmcid>PMC4230144</pmcid><pubmed_authors>You L</pubmed_authors><pubmed_authors>Peng Y</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Gu W</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Pan L</pubmed_authors></additional><is_claimable>false</is_claimable><name>MiR-378 overexpression attenuates high glucose-suppressed osteogenic differentiation through targeting CASP3 and activating PI3K/Akt signaling pathway.</name><description>Hyperglycemia is one of the possible causes for osteoporosis and bone fracture in diabetes mellitus. Here we modeled diabetes-induced osteoporosis in vitro using preosteoblastic cell line MC3T3-E1 and a diabetic mice model for in vivo studies. We found that in addition to reducing osteoblast viability and differentiation (mineralization), culture in elevated glucose down regulated microRNA-378 (miR-378) expression but ectopic miR-378 expression reversed the effects of high glucose. We identified caspase-3 (CASP3) as a target of miR-378 and showed that miR-378 repressed CASP3 mRNA and protein expression under high glucose condition. We further showed that both miR-378 expression and CASP3 silencing independently restored alkaline phosphatase (ALP) activity and the expression of osteoblastic</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2025-04-25T20:32:38.975Z</modification><creation>2025-04-06T08:23:22.25Z</creation></dates><accession>S-EPMC4230144</accession><cross_references><pubmed>25400823</pubmed></cross_references></HashMap>