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dc.contributor.authorGonzález Cabeza, Alicia Verónica 
dc.contributor.authorAlonso González, Carolina 
dc.contributor.authorGonzález González, Alicia
dc.contributor.authorMenéndez Menéndez, Javier
dc.contributor.authorCos Corral, Samuel 
dc.contributor.authorMartínez Campa, Carlos Manuel 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-03-02T15:06:13Z
dc.date.available2022-03-02T15:06:13Z
dc.date.issued2021
dc.identifier.issn2072-6694
dc.identifier.otherSAF2016-77103-Pes_ES
dc.identifier.urihttp://hdl.handle.net/10902/24097
dc.description.abstractMelatonin is a hormone with different functions, antitumor actions being one of the most studied. Among its antitumor mechanisms is its ability to inhibit angiogenesis. Melatonin shows antiangiogenic effects in several types of tumors. Combination of melatonin and chemotherapeutic agents have a synergistic effect inhibiting angiogenesis. One of the undesirable effects of chemotherapy is the induction of pro-angiogenic factors, whilst the addition of melatonin is able to overcome these undesirable effects. This protective effect of the pineal hormone against angiogenesis might be one of the mechanisms underlying its anticancer effect, explaining, at least in part, why melatonin administration increases the sensitivity of tumors to the inhibitory effects exerted by ordinary chemotherapeutic agents. Melatonin has the ability to turn cancer totally resistant to chemotherapeutic agents into a more sensitive chemotherapy state. Definitely, melatonin regulates the expression and/or activity of many factors involved in angiogenesis which levels are affected (either positively or negatively) by chemotherapeutic agents. In addition, the pineal hormone has been proposed as a radiosensitizer, increasing the oncostatic effects of radiation on tumor cells. This review serves as a synopsis of the interaction between melatonin and angiogenesis, and we will outline some antiangiogenic mechanisms through which melatonin sensitizes cancer cells to treatments, such as radiotherapy or chemotherapy.es_ES
dc.description.sponsorshipFunding: The present study was funded by grants from the Spanish Economy and Competitiveness Ministry (SAF2016-77103-P), from University of Cantabria (Proyectos Puente 2020), and from Instituto de Investigación Sanitaria Valdecilla (IDIVAL) (APG/12).es_ES
dc.format.extent27 p.es_ES
dc.language.isoenges_ES
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.es_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceCancers (Basel) . 2021 Jun 29;13(13):3263es_ES
dc.subject.otherMelatonines_ES
dc.subject.otherAngiogenesises_ES
dc.subject.otherChemotherapyes_ES
dc.subject.otherRadiotherapyes_ES
dc.subject.otherBreast canceres_ES
dc.subject.otherAntiangiogenic actionses_ES
dc.titleMelatonin as an adjuvant to antiangiogenic cancer treatmentses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.3390/cancers 13133263es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3390/cancers13133263
dc.type.versionpublishedVersiones_ES


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Mostrar el registro sencillo

© 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.Excepto si se señala otra cosa, la licencia del ítem se describe como © 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.