Co-adjuvant therapy efficacy of catechin and procyanidin b2 with docetaxel on hormone-related cancers in vitro

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psiquiatría, Radioloxía, Saúde Pública, Enfermaría e Medicina
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica
dc.contributor.authorNúñez Iglesias, María Jesús
dc.contributor.authorNovío Mallón, Silvia
dc.contributor.authorGarcía Santiago, Carlota
dc.contributor.authorPérez Muñuzuri, Mª Elena
dc.contributor.authorMartínez, María-Carmen
dc.contributor.authorSantiago, José-Luis
dc.contributor.authorBoso, Susana
dc.contributor.authorGago, Pilar
dc.contributor.authorFreire-Garabal Núñez, Manuel
dc.date.accessioned2025-10-24T11:49:01Z
dc.date.available2025-10-24T11:49:01Z
dc.date.issued2021-07-02
dc.description.abstractProstate (PC) and breast cancer (BC) are heterogeneous hormonal cancers. Treatment resistance and adverse effects are the main limitations of conventional chemotherapy treatment. The use of sensitizing agents could improve the effectiveness of chemotherapeutic drugs as well as obviate these limitations. This study analyzes the effect of single catechin (CAT), procyanidin B2 (ProB2) treatment as well as the co-adjuvant treatment of each of these compounds with docetaxel (DOCE). We used PC- and BC-derived cell lines (PC3, DU-145, T47D, MCF-7 and MDA-MB-231). The short and long-term pro-apoptotic, anti-proliferative and anti-migratory effects were analyzed. RT-qPCR was used to discover molecular bases of the therapeutic efficacy of these compounds. ProB2 treatment induced a two- to five-fold increase in anti-proliferative and pro-apoptotic effects compared to single DOCE treatment, and also had a more sensitizing effect than DOCE on DU145 cells. Regarding BC cells, ProB2- and CAT-mediated sensitization to DOCE anti-proliferative and pro-apoptotic effects was cell-independent and cell-dependent, respectively. Combined treatment led to high-efficacy effects on MCF-7 cells, which were associated to the up-regulation of CDKN1A, BAX, caspase 9 and E-cadherin mRNA under combined treatment compared to single DOCE treatment. CAT and ProB2 can enhance the efficacy of DOCE therapy on PC and BC cells by the sensitizing mechanism.
dc.description.peerreviewedSI
dc.description.sponsorshipThis research included in Interreg Atlantic Area Programme 2014–2020 was funded by European Regional Development Fund (ERDF) under management of Centro para el Desarrollo Tecnológico Industrial (CDTI). INNGAL-AGROMARSALUD 2013 project [grant number ITC-20133014].
dc.identifier.citationNúñez-Iglesias, M.J.; Novio, S.; García, C.; Pérez-Muñuzuri, M.E.; Martínez, M.-C.; Santiago, J.-L.; Boso, S.; Gago, P.; Freire-Garabal, M. Co-Adjuvant Therapy Efficacy of Catechin and Procyanidin B2 with Docetaxel on Hormone-Related Cancers In Vitro. Int. J. Mol. Sci. 2021, 22, 7178. https://doi.org/10.3390/ ijms22137178
dc.identifier.doi10.3390/ijms22137178
dc.identifier.issn1422-0067
dc.identifier.urihttps://hdl.handle.net/10347/43388
dc.journal.titleInternational Journal of Molecular Sciences
dc.language.isoeng
dc.page.final29
dc.page.initial1
dc.publisherMDPI
dc.relation.projectID20133014
dc.relation.publisherversionhttps://doi.org/10.3390/ijms22137178
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license. Attribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAntitumor activity
dc.subjectCatechin
dc.subjectDocetaxel
dc.subjectDocetaxel-sensitization
dc.subjectHormone-related cancer
dc.subjectNatural substances
dc.subjectPlant co-adjuvant therapy
dc.subjectProcyanidin
dc.titleCo-adjuvant therapy efficacy of catechin and procyanidin b2 with docetaxel on hormone-related cancers in vitro
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number22
dspace.entity.typePublication
relation.isAuthorOfPublication5cbecf8b-bcf0-4fb9-a778-0c8609d1cee2
relation.isAuthorOfPublication2af53262-a340-48fa-a042-b862b2df6f1d
relation.isAuthorOfPublication6edab564-dfce-4586-95bb-0977f87f74bd
relation.isAuthorOfPublication.latestForDiscovery5cbecf8b-bcf0-4fb9-a778-0c8609d1cee2

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