<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Darvishian Farbod</submitter><species>Homo sapiens</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-24824</full_dataset_link><project>EurocanPlatform</project><abstract>To identify genes differentially modulated by anti-miR-182 treatment in a liver melanoma metastasis mouse model. Targeting oncogenic microRNAs is emerging as a promising strategy for cancer therapy. Here we provide proof-of-principle for the safety and efficacy of miRNA targeting against metastatic tumors. We tested the effect of targeting miR-182, a pro-metastatic miRNA frequently overexpressed in melanoma, whose silencing represses invasion and induces apoptosis in vitro. In particular, we assessed the effect of anti-miR-182 oligonucleotides synthesized with 2’ sugar modifications and a phosphorothioate backbone in a mouse model of melanoma liver metastasis. Luciferase imaging showed that mice treated with anti-miR-182 had an appreciably lower burden of liver metastases compared to the c</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array</experiment_type><data_source>EurocanPlatform</data_source><pubmed_authors>Levin Brandi</pubmed_authors><pubmed_authors>Segura Miguel</pubmed_authors><pubmed_authors>Osman Iman</pubmed_authors><pubmed_authors>Menendez Silvia</pubmed_authors><pubmed_authors>Zavadil Jiri</pubmed_authors><pubmed_authors>Darvishian Farbod</pubmed_authors><pubmed_authors>Huynh Chanh</pubmed_authors><pubmed_authors>Meruelo Daniel</pubmed_authors><pubmed_authors>Hernando Eva</pubmed_authors><pubmed_authors>Gaziel Avita</pubmed_authors><pubmed_authors>Chiriboga Luis</pubmed_authors></additional><is_claimable>false</is_claimable><name>Identification of genes and molecular pathways associated with anti-miR-182 treatment</name><description>To identify genes differentially modulated by anti-miR-182 treatment in a liver melanoma metastasis mouse model. Targeting oncogenic microRNAs is emerging as a promising strategy for cancer therapy. Here we provide proof-of-principle for the safety and efficacy of miRNA targeting against metastatic tumors. We tested the effect of targeting miR-182, a pro-metastatic miRNA frequently overexpressed in melanoma, whose silencing represses invasion and induces apoptosis in vitro. In particular, we assessed the effect of anti-miR-182 oligonucleotides synthesized with 2’ sugar modifications and a phosphorothioate backbone in a mouse model of melanoma liver metastasis. Luciferase imaging showed that mice treated with anti-miR-182 had an appreciably lower burden of liver metastases compared to the c</description><dates><release>2016-04-14T13:48:51Z</release><modification>2016-04-14T13:48:51Z</modification><creation>2016-04-14T13:48:51Z</creation></dates><accession>S-ECPF-GEOD-24824</accession><cross_references><GEO>GSE24824</GEO><ArrayExpress>E-GEOD-24824</ArrayExpress><EFO>EFO_0000756</EFO><EFO>EFO_0003942</EFO><ArrayExpress files>E-GEOD-24824</ArrayExpress files></cross_references></HashMap>