<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rosso M</submitter><funding>Consejo Nacional de Investigaciones Científicas y Técnicas</funding><funding>Fundación Alberto J. Roemmers</funding><funding>FP7 People: Marie-Curie Actions</funding><funding>Instituto Nacional del Cáncer</funding><funding>Agencia Nacional de Promoción Científica y Tecnológica</funding><pagination>5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6507066</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Breast cancer (BC) is the most common female cancer and the leading cause of cancer death in women worldwide. Alterations in epithelial cadherin (E-cadherin) expression and functions are associated to BC, but the underlying molecular mechanisms have not been fully elucidated. We have previously reported a novel human E-cadherin splice variant (E-cadherin variant) mRNA. Stable transfectants in MCF-7 human BC cells (MCF7Ecadvar) depicted fibroblast-like cell morphology, E-cadherin wild-type downregulation, and other molecular changes characteristic of the epithelial-to-mesenchymal transition process, reduced cell-cell adhesion, and increased cell migration and invasion. In this study, a two-dimensional differential gel electrophoresis (2D-DIGE) combined with mass spectrome</pubmed_abstract><journal>Cancer &amp; metabolism</journal><pubmed_title>Characterization of the molecular changes associated with the overexpression of a novel epithelial cadherin splice variant mRNA in a breast cancer model using proteomics and bioinformatics approaches: identification of changes in cell metabolism and an increased expression of lactate dehydrogenase B.</pubmed_title><pmcid>PMC6507066</pmcid><funding_grant_id>2016-2017</funding_grant_id><funding_grant_id>PIP740</funding_grant_id><funding_grant_id>2011-2013</funding_grant_id><funding_grant_id>PICT SU 1072</funding_grant_id><funding_grant_id>2014-2015</funding_grant_id><funding_grant_id>PIP887</funding_grant_id><funding_grant_id>269285</funding_grant_id><pubmed_authors>Matos ML</pubmed_authors><pubmed_authors>Besso MJ</pubmed_authors><pubmed_authors>Reventos J</pubmed_authors><pubmed_authors>Canals F</pubmed_authors><pubmed_authors>Quevedo Cuenca JO</pubmed_authors><pubmed_authors>Rosso M</pubmed_authors><pubmed_authors>Vazquez-Levin MH</pubmed_authors><pubmed_authors>Lapyckyj L</pubmed_authors><pubmed_authors>Monge M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Characterization of the molecular changes associated with the overexpression of a novel epithelial cadherin splice variant mRNA in a breast cancer model using proteomics and bioinformatics approaches: identification of changes in cell metabolism and an increased expression of lactate dehydrogenase B.</name><description>&lt;h4>Background&lt;/h4>Breast cancer (BC) is the most common female cancer and the leading cause of cancer death in women worldwide. Alterations in epithelial cadherin (E-cadherin) expression and functions are associated to BC, but the underlying molecular mechanisms have not been fully elucidated. We have previously reported a novel human E-cadherin splice variant (E-cadherin variant) mRNA. Stable transfectants in MCF-7 human BC cells (MCF7Ecadvar) depicted fibroblast-like cell morphology, E-cadherin wild-type downregulation, and other molecular changes characteristic of the epithelial-to-mesenchymal transition process, reduced cell-cell adhesion, and increased cell migration and invasion. In this study, a two-dimensional differential gel electrophoresis (2D-DIGE) combined with mass spectrome</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-05-07T02:14:56.396Z</modification><creation>2019-06-06T23:29:04Z</creation></dates><accession>S-EPMC6507066</accession><cross_references><pubmed>31086659</pubmed><doi>10.1186/s40170-019-0196-9</doi></cross_references></HashMap>