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<dc:creator>González-Vallinas Garrachón, Margarita</dc:creator>
<dc:creator>Molina, Susana</dc:creator>
<dc:creator>Vicente, Gonzalo</dc:creator>
<dc:creator>Zarza, Virginia</dc:creator>
<dc:creator>Martín Hernández, Roberto</dc:creator>
<dc:creator>García Risco, Mónica R.</dc:creator>
<dc:creator>Fornari, Tiziana</dc:creator>
<dc:creator>Reglero, Guillermo</dc:creator>
<dc:creator>Ramírez de Molina, Ana</dc:creator>
<dc:date>2014</dc:date>
<dc:description>Producción Científica</dc:description>
<dc:description>Colorectal and pancreatic cancers remain important contributors to cancer mortality burden and, therefore, new&#xd;
therapeutic approaches are urgently needed. Rosemary (Rosmarinus officinalis L.) extracts and its components have been&#xd;
reported as natural potent antiproliferative agents against cancer cells. However, to potentially apply rosemary as a&#xd;
complementary approach for cancer therapy, additional information regarding the most effective composition, its&#xd;
antitumor effect in vivo and its main molecular mediators is still needed. In this work, five carnosic acid-rich supercritical&#xd;
rosemary extracts with different chemical compositions have been assayed for their antitumor activity both in vivo (in nude&#xd;
mice) and in vitro against colon and pancreatic cancer cells. We found that the antitumor effect of carnosic acid together&#xd;
with carnosol was higher than the sum of their effects separately, which supports the use of the rosemary extract as a&#xd;
whole. In addition, gene and microRNA expression analyses have been performed to ascertain its antitumor mechanism,&#xd;
revealing that up-regulation of the metabolic-related gene GCNT3 and down-regulation of its potential epigenetic&#xd;
modulator miR-15b correlate with the antitumor effect of rosemary. Moreover, plasmatic miR-15b down-regulation was&#xd;
detected after in vivo treatment with rosemary. Our results support the use of carnosic acid-rich rosemary extract as a&#xd;
complementary approach in colon and pancreatic cancer and indicate that GCNT3 expression may be involved in its&#xd;
antitumor mechanism and that miR-15b might be used as a non-invasive biomarker to monitor rosemary anticancer effect.</dc:description>
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<dc:identifier>http://uvadoc.uva.es/handle/10324/42590</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>Public Library of Science</dc:publisher>
<dc:subject>3207.13 Oncología</dc:subject>
<dc:title>Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
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