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dc.creatorGuillén Mancina, Emilioes
dc.creatorJiménez Alonso, Julio Josées
dc.creatorCalderón Montaño, José Manueles
dc.creatorJiménez González, Víctores
dc.creatorDíaz Ortega, Patriciaes
dc.creatorBurgos Morón, Estefaníaes
dc.creatorLópez Lázaro, Migueles
dc.date.accessioned2023-03-16T16:10:36Z
dc.date.available2023-03-16T16:10:36Z
dc.date.issued2023
dc.identifier.citationGuillén Mancina, E., Jiménez Alonso, J.J., Calderón Montaño, J.M., Jiménez González, V., Díaz Ortega, P., Burgos Morón, E. y López Lázaro, M. (2023). Artificial Diets with Selective Restriction of Amino Acids and Very Low Levels of Lipids Induce Anticancer Activity in Mice with Metastatic Triple-Negative Breast Cancer. Cancers, 15 (5), 1540. https://doi.org/10.3390/cancers15051540.
dc.identifier.issn2072-6694es
dc.identifier.urihttps://hdl.handle.net/11441/143415
dc.description.abstractCurrent treatments for patients with metastatic triple negative breast cancer (TNBC) are generally ineffective. This manuscript shows for the first time that the survival of mice with metastatic TNBC can be markedly increased through dietary manipulation. Our study revealed that the survival of some mice with metastatic TNBC was increased by replacing their normal diet with artificial diets in which the levels of amino acids (AAs) are manipulated, and the levels of lipids are markedly reduced. The anticancer activity of this non-pharmacological strategy was higher than that of drugs currently used in the treatment of patients with metastatic TNBC. This anticancer strategy also increased the survival of mice with other types of metastatic cancers. Manipulation of AA and lipid levels with artificial diets may be a useful strategy to treat patients with metastatic TNBC and other types of disseminated cancer.es
dc.description.abstractPatients with metastatic triple negative breast cancer (TNBC) need new therapies to improve the low survival rates achieved with standard treatments. In this work, we show for the first time that the survival of mice with metastatic TNBC can be markedly increased by replacing their normal diet with artificial diets in which the levels of amino acids (AAs) and lipids are strongly manipulated. After observing selective anticancer activity in vitro, we prepared five artificial diets and evaluated their anticancer activity in a challenging model of metastatic TNBC. The model was established by injecting 4T1 murine TNBC cells into the tail vein of immunocompetent BALB/cAnNRj mice. First-line drugs doxorubicin and capecitabine were also tested in this model. AA manipulation led to modest improvements in mice survival when the levels of lipids were normal. Reducing lipid levels to 1% markedly improved the activity of several diets with different AA content. Some mice fed the artificial diets as monotherapy lived much longer than mice treated with doxorubicin and capecitabine. An artificial diet without 10 non-essential AAs, with reduced levels of essential AAs, and with 1% lipids improved the survival not only of mice with TNBC but also of mice with other types of metastatic cancers.es
dc.description.sponsorshipJunta de Andalucía 2017/CTS-657, 2019/CTS-657, 2021/CTS-657es
dc.description.sponsorshipUniversidad de Sevilla VIPPIT-2019-I.5, VIPPIT-2020-I.5, VIPPIT-2021-I.5es
dc.formatapplication/pdfes
dc.format.extent28 p.es
dc.language.isoenges
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)es
dc.relation.ispartofCancers, 15 (5), 1540.
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAmino acidses
dc.subjectLipidses
dc.subjectDietes
dc.subjectLow-fat dietes
dc.subjectCancer therapyes
dc.subjectCancer metabolismes
dc.subjectTriple-negative breast canceres
dc.subjectLung canceres
dc.subjectMelanomaes
dc.subjectColorectal canceres
dc.subjectOvarian canceres
dc.subjectMetastasises
dc.titleArtificial Diets with Selective Restriction of Amino Acids and Very Low Levels of Lipids Induce Anticancer Activity in Mice with Metastatic Triple-Negative Breast Canceres
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Farmacologíaes
dc.relation.projectID2017/CTS-657es
dc.relation.projectID2019/CTS-657es
dc.relation.projectID2021/CTS-657es
dc.relation.projectIDVIPPIT-2019-I.5es
dc.relation.projectIDVIPPIT-2020-I.5es
dc.relation.projectIDVIPPIT-2021-I.5es
dc.relation.publisherversionhttps://doi.org/10.3390/cancers15051540es
dc.identifier.doi10.3390/cancers15051540es
dc.journaltitleCancerses
dc.publication.volumen15es
dc.publication.issue5es
dc.publication.initialPage1540es
dc.contributor.funderJunta de Andalucíaes
dc.contributor.funderUniversidad de Sevillaes

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Atribución 4.0 Internacional
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