<?xml version="1.0" encoding="UTF-8"?>
<collection>
<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1016/j.trsl.2018.03.004</dc:identifier><dc:language>eng</dc:language><dc:creator>Alvarez-Arguedas, S.</dc:creator><dc:creator>Uranga, S.</dc:creator><dc:creator>Martín, M.</dc:creator><dc:creator>Elizalde, J.</dc:creator><dc:creator>Gomez, A.B.</dc:creator><dc:creator>Julián, E.</dc:creator><dc:creator>Nardelli-Haefliger, D.</dc:creator><dc:creator>Martín, C.</dc:creator><dc:creator>Aguilo, N.</dc:creator><dc:title>Therapeutic efficacy of the live-attenuated Mycobacterium tuberculosis vaccine, MTBVAC, in a preclinical model of bladder cancer</dc:title><dc:identifier>ART-2018-106599</dc:identifier><dc:description>Intravesical instillation of bacillus Calmette-Guérin (BCG) has been a first-line therapy for non–muscle-invasive bladder cancer for the last 4 decades. However, this treatment causes serious adverse events in a significant number of patients and a substantial percentage of recurrence episodes. MTBVAC is a live-attenuated vaccine derived from a Mycobacterium tuberculosis clinical isolate and is currently under evaluation in clinical trials to replace BCG as a tuberculosis vaccine. Here, we describe for the first time the potential of MTBVAC as a bladder cancer therapy in vitro and in vivo in a preclinical model. MTBVAC colonized human bladder tumor cells to a much greater extent than BCG via a mechanism mediated by macropinocytosis and induced cell growth inhibition after internalization. In vivo testing in an orthotopic murine model of bladder cancer demonstrated a higher antitumor effect of MTBVAC in experimental conditions in which BCG did not work. Our data encourage further studies to support the possible application of MTBVAC as a new immunotherapeutic agent for bladder cancer.</dc:description><dc:date>2018</dc:date><dc:source>http://zaguan.unizar.es/record/79139</dc:source><dc:doi>10.1016/j.trsl.2018.03.004</dc:doi><dc:identifier>http://zaguan.unizar.es/record/79139</dc:identifier><dc:identifier>oai:zaguan.unizar.es:79139</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/DGA/FSE</dc:relation><dc:relation>info:eu-repo/grantAgreement/ES/MINECO/BIO2014-5258P</dc:relation><dc:identifier.citation>Translational Research 197 (2018), 32-42</dc:identifier.citation><dc:rights>by-nc-nd</dc:rights><dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

</collection>