Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer

Colorectal and pancreatic cancers remain important contributors to cancer mortality burden and, therefore, new therapeutic approaches are urgently needed. Rosemary (Rosmarinus officinalis L.) extracts and its components have been reported as natural potent antiproliferative agents against cancer cells. However, to potentially apply rosemary as a complementary approach for cancer therapy, additional information regarding the most effective composition, its antitumor effect in vivo and its main molecular mediators is still needed. In this work, five carnosic acid-rich supercritical rosemary extracts with different chemical compositions have been assayed for their antitumor activity both in vivo (in nude mice) and in vitro against colon and pancreatic cancer cells. We found that the antitumor effect of carnosic acid together with carnosol was higher than the sum of their effects separately, which supports the use of the rosemary extract as a whole. In addition, gene and microRNA expression analyses have been performed to ascertain its antitumor mechanism, revealing that up-regulation of the metabolic-related gene GCNT3 and down-regulation of its potential epigenetic modulator miR-15b correlate with the antitumor effect of rosemary. Moreover, plasmatic miR-15b down-regulation was detected after in vivo treatment with rosemary. Our results support the use of carnosic acid-rich rosemary extract as a complementary approach in colon and pancreatic cancer and indicate that GCNT3 expression may be involved in its antitumor mechanism and that miR-15b might be used as a non-invasive biomarker to monitor rosemary anticancer effect. © 2014 González-Vallinas et al.

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Main Authors: González-Vallinas, Margarita, Molina, Susana, Vicente, G., Zarza, Virginia, Martín-Hernández, Roberto, García-Risco, Mónica R., Fornari, Tiziana, Reglero, Guillermo, Ramírez de Molina, Ana
Other Authors: Comunidad de Madrid
Format: artículo biblioteca
Published: Public Library of Science 2014
Online Access:http://hdl.handle.net/10261/113510
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/100012818
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spelling dig-cial-es-10261-1135102021-12-28T16:23:41Z Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer González-Vallinas, Margarita Molina, Susana Vicente, G. Zarza, Virginia Martín-Hernández, Roberto García-Risco, Mónica R. Fornari, Tiziana Reglero, Guillermo Ramírez de Molina, Ana Comunidad de Madrid Ministerio de Ciencia e Innovación (España) European Commission Colorectal and pancreatic cancers remain important contributors to cancer mortality burden and, therefore, new therapeutic approaches are urgently needed. Rosemary (Rosmarinus officinalis L.) extracts and its components have been reported as natural potent antiproliferative agents against cancer cells. However, to potentially apply rosemary as a complementary approach for cancer therapy, additional information regarding the most effective composition, its antitumor effect in vivo and its main molecular mediators is still needed. In this work, five carnosic acid-rich supercritical rosemary extracts with different chemical compositions have been assayed for their antitumor activity both in vivo (in nude mice) and in vitro against colon and pancreatic cancer cells. We found that the antitumor effect of carnosic acid together with carnosol was higher than the sum of their effects separately, which supports the use of the rosemary extract as a whole. In addition, gene and microRNA expression analyses have been performed to ascertain its antitumor mechanism, revealing that up-regulation of the metabolic-related gene GCNT3 and down-regulation of its potential epigenetic modulator miR-15b correlate with the antitumor effect of rosemary. Moreover, plasmatic miR-15b down-regulation was detected after in vivo treatment with rosemary. Our results support the use of carnosic acid-rich rosemary extract as a complementary approach in colon and pancreatic cancer and indicate that GCNT3 expression may be involved in its antitumor mechanism and that miR-15b might be used as a non-invasive biomarker to monitor rosemary anticancer effect. © 2014 González-Vallinas et al. This work was supported by the Spanish Ministry of Science and Innovation (Plan Nacional I+D+i AGL2010-21565, RyC 2008-03734; IPT-2011-1248-060000); Comunidad de Madrid (ALIBIRD, S2009/AGR-1469); and European Union Structural Funds. Peer Reviewed 2015-04-10T11:03:37Z 2015-04-10T11:03:37Z 2014 2015-04-10T11:03:38Z artículo http://purl.org/coar/resource_type/c_6501 doi: 10.1371/journal.pone.0098556 issn: 1932-6203 PLoS ONE 9(6): e98556 (2014) http://hdl.handle.net/10261/113510 10.1371/journal.pone.0098556 http://dx.doi.org/10.13039/501100004837 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/100012818 24892299 #PLACEHOLDER_PARENT_METADATA_VALUE# S2009/AGR-1469/ALIBIRD Publisher's version http://dx.doi.org/10.1371/journal.pone.0098556 Sí open Public Library of Science
institution CIAL ES
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country España
countrycode ES
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access En linea
databasecode dig-cial-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del CIAL España
description Colorectal and pancreatic cancers remain important contributors to cancer mortality burden and, therefore, new therapeutic approaches are urgently needed. Rosemary (Rosmarinus officinalis L.) extracts and its components have been reported as natural potent antiproliferative agents against cancer cells. However, to potentially apply rosemary as a complementary approach for cancer therapy, additional information regarding the most effective composition, its antitumor effect in vivo and its main molecular mediators is still needed. In this work, five carnosic acid-rich supercritical rosemary extracts with different chemical compositions have been assayed for their antitumor activity both in vivo (in nude mice) and in vitro against colon and pancreatic cancer cells. We found that the antitumor effect of carnosic acid together with carnosol was higher than the sum of their effects separately, which supports the use of the rosemary extract as a whole. In addition, gene and microRNA expression analyses have been performed to ascertain its antitumor mechanism, revealing that up-regulation of the metabolic-related gene GCNT3 and down-regulation of its potential epigenetic modulator miR-15b correlate with the antitumor effect of rosemary. Moreover, plasmatic miR-15b down-regulation was detected after in vivo treatment with rosemary. Our results support the use of carnosic acid-rich rosemary extract as a complementary approach in colon and pancreatic cancer and indicate that GCNT3 expression may be involved in its antitumor mechanism and that miR-15b might be used as a non-invasive biomarker to monitor rosemary anticancer effect. © 2014 González-Vallinas et al.
author2 Comunidad de Madrid
author_facet Comunidad de Madrid
González-Vallinas, Margarita
Molina, Susana
Vicente, G.
Zarza, Virginia
Martín-Hernández, Roberto
García-Risco, Mónica R.
Fornari, Tiziana
Reglero, Guillermo
Ramírez de Molina, Ana
format artículo
author González-Vallinas, Margarita
Molina, Susana
Vicente, G.
Zarza, Virginia
Martín-Hernández, Roberto
García-Risco, Mónica R.
Fornari, Tiziana
Reglero, Guillermo
Ramírez de Molina, Ana
spellingShingle González-Vallinas, Margarita
Molina, Susana
Vicente, G.
Zarza, Virginia
Martín-Hernández, Roberto
García-Risco, Mónica R.
Fornari, Tiziana
Reglero, Guillermo
Ramírez de Molina, Ana
Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
author_sort González-Vallinas, Margarita
title Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
title_short Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
title_full Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
title_fullStr Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
title_full_unstemmed Expression of MicroRNA-15b and the glycosyltransferase GCNT3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
title_sort expression of microrna-15b and the glycosyltransferase gcnt3 correlates with antitumor efficacy of rosemary diterpenes in colon and pancreatic cancer
publisher Public Library of Science
publishDate 2014
url http://hdl.handle.net/10261/113510
http://dx.doi.org/10.13039/501100004837
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/100012818
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