<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Luengo-Gil G</submitter><funding>Instituto de Salud Carlos III</funding><funding>Fundación Salud 2000</funding><funding>Ministerio de Educación, Cultura y Deporte</funding><pagination>e0194638</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5884522</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Angiogenesis is a key process for tumor progression and a target for treatment. However, the regulation of breast cancer angiogenesis and its relevance for clinical resistance to antiangiogenic drugs is still incompletely understood. Recent developments on the contribution of microRNA to tumor angiogenesis and on the oncogenic effects of miR-17-92, a miRNA cluster, point to their potential role on breast cancer angiogenesis. The aim of this work was to establish the contribution of miR-20a, a member of miR-17-92 cluster, to tumor angiogenesis in patients with invasive breast carcinoma.&lt;h4>Methods&lt;/h4>Tube-formation in vitro assays with conditioned medium from MCF7 and MDA-MB-231 breast cancer cell lines were performed after transfection with miR-20a and anti-miR20a. For </pubmed_abstract><journal>PloS one</journal><pubmed_title>Angiogenic role of miR-20a in breast cancer.</pubmed_title><pmcid>PMC5884522</pmcid><funding_grant_id>FPU16/06537</funding_grant_id><funding_grant_id>Ayuda Merck Serono de Investigación en Oncología 2012</funding_grant_id><funding_grant_id>PI12/02877</funding_grant_id><pubmed_authors>Gonzalez-Billalabeitia E</pubmed_authors><pubmed_authors>Navarro Manzano E</pubmed_authors><pubmed_authors>Garcia-Garre E</pubmed_authors><pubmed_authors>Perez-Henarejos SA</pubmed_authors><pubmed_authors>Luengo-Gil G</pubmed_authors><pubmed_authors>Garcia-Martinez E</pubmed_authors><pubmed_authors>Chaves-Benito A</pubmed_authors><pubmed_authors>Ayala de la Pena F</pubmed_authors><pubmed_authors>Vicente V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Angiogenic role of miR-20a in breast cancer.</name><description>&lt;h4>Background&lt;/h4>Angiogenesis is a key process for tumor progression and a target for treatment. However, the regulation of breast cancer angiogenesis and its relevance for clinical resistance to antiangiogenic drugs is still incompletely understood. Recent developments on the contribution of microRNA to tumor angiogenesis and on the oncogenic effects of miR-17-92, a miRNA cluster, point to their potential role on breast cancer angiogenesis. The aim of this work was to establish the contribution of miR-20a, a member of miR-17-92 cluster, to tumor angiogenesis in patients with invasive breast carcinoma.&lt;h4>Methods&lt;/h4>Tube-formation in vitro assays with conditioned medium from MCF7 and MDA-MB-231 breast cancer cell lines were performed after transfection with miR-20a and anti-miR20a. For </description><dates><release>2018-01-01T00:00:00Z</release><publication>2018</publication><modification>2025-04-21T19:57:31.362Z</modification><creation>2019-03-26T23:29:13Z</creation></dates><accession>S-EPMC5884522</accession><cross_references><pubmed>29617404</pubmed><doi>10.1371/journal.pone.0194638</doi></cross_references></HashMap>