<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(28)</volume><submitter>Liu X</submitter><pubmed_abstract>Growing evidence indicates that microRNA (miRNA) plays a vital role in progression and metastasis of gastric cancer (GC). However, the underlying mechanism of miRNA-mediated metastasis has not been fully understood. Recently, miRNA-940 (miR-940) was found to be overexpressed in GC, which correlated with malignant progression and poor survival. Mechanistically, we found that miR-940 promoted GC cell migration, invasion, and metastasis in vivo by directly and functionally repressing the expression of Zinc Finger Transcription Factor 24 (ZNF24). Importantly, upregulation of ZNF24 could re-inhibit miR-940-induced migration and invasion. Hence, we demonstrated the oncogenic role of miR-940 in GC, finding that miR-940 promoted GC progression by directly downregulating ZNF24 expression, and targeting miR-940 could serve as a novel strategy for future GC therapy.</pubmed_abstract><journal>Oncotarget</journal><pagination>25418-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4694841</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MicroRNA-940 promotes tumor cell invasion and metastasis by downregulating ZNF24 in gastric cancer.</pubmed_title><pmcid>PMC4694841</pmcid><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Sun M</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zhang Z</pubmed_authors><pubmed_authors>Gan L</pubmed_authors><pubmed_authors>Ge X</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Chang J</pubmed_authors><pubmed_authors>Tang W</pubmed_authors></additional><is_claimable>false</is_claimable><name>MicroRNA-940 promotes tumor cell invasion and metastasis by downregulating ZNF24 in gastric cancer.</name><description>Growing evidence indicates that microRNA (miRNA) plays a vital role in progression and metastasis of gastric cancer (GC). However, the underlying mechanism of miRNA-mediated metastasis has not been fully understood. Recently, miRNA-940 (miR-940) was found to be overexpressed in GC, which correlated with malignant progression and poor survival. Mechanistically, we found that miR-940 promoted GC cell migration, invasion, and metastasis in vivo by directly and functionally repressing the expression of Zinc Finger Transcription Factor 24 (ZNF24). Importantly, upregulation of ZNF24 could re-inhibit miR-940-induced migration and invasion. Hence, we demonstrated the oncogenic role of miR-940 in GC, finding that miR-940 promoted GC progression by directly downregulating ZNF24 expression, and targeting miR-940 could serve as a novel strategy for future GC therapy.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep</publication><modification>2025-04-04T03:42:13.863Z</modification><creation>2019-03-27T02:05:56Z</creation></dates><accession>S-EPMC4694841</accession><cross_references><pubmed>26317898</pubmed><doi>10.18632/oncotarget.4456</doi></cross_references></HashMap>