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dc.contributor.authorJara-Gutiérrez, Carlos
dc.contributor.authorMercado, Luis
dc.contributor.authorPaz-Araos, Marilyn
dc.contributor.authorHoward, Carolyn
dc.contributor.authorParraga, Mario
dc.contributor.authorEscobar, Camila
dc.contributor.authorMellado, Marco
dc.contributor.authorMadrid, Alejandro
dc.contributor.authorMontenegro, Iván
dc.contributor.authorSantana, Paula
dc.contributor.authorMurgas, Paola
dc.contributor.authorJimenez-Jara, Cristina
dc.contributor.authorGonzález-Olivares, Luis Guillermo
dc.contributor.authorAhumada, Manuel
dc.contributor.authorVillena, Joan
dc.date.accessioned2024-04-09T22:55:28Z
dc.date.available2024-04-09T22:55:28Z
dc.date.issued2024
dc.identifier10.1186/s12906-024-04341-4
dc.identifier.issn26627671
dc.identifier.urihttps://hdl.handle.net/20.500.12728/10323
dc.description.abstractBackground: Standard cancer treatments show a lack of selectivity that has led to the search for new strategies against cancer. The selective elimination of cancer cells modulating the redox environment, known as “selective oxycution”, has emerged as a viable alternative. This research focuses on characterizing the unexplored Escallonia genus plant extracts and evaluating their potential effects on cancer’s redox balance, cytotoxicity, and activation of death pathways. Methods: 36 plant extracts were obtained from 4 different species of the Escallonia genus (E. illinita C. Presl, E. rubra (Ruiz & Pav.) Pers., E. revoluta (Ruiz & Pav.) Pers., and E. pulverulenta (Ruiz & Pav.) Pers.), which were posteriorly analyzed by their phytoconstituents, antioxidant capacity, and GC-MS. Further, redox balance assays (antioxidant enzymes, oxidative damage, and transcription factors) and cytotoxic effects (SRB, ∆Ψmt, and caspases actives) of those plant extracts were analyzed on four cell lines (HEK-293T, MCF-7, HT-29, and PC-3). Results: 36 plant extracts were obtained, and their phytoconstituents and antioxidant capacity were established. Further, only six extracts had EC50 values < 10 µg*mL− 1, indicating high toxicity against the tested cells. From those, two plant extracts were selective against different cancer cell lines: the hexane extract of E. pulverulenta´s stem was selective for HT-29, and the ethyl acetate extract of E. rubra´s stem was selective for PC-3. Both extracts showed unbalanced redox effects and promoted selective cell death. Conclusions: This is the first study proving “selective oxycution” induced by Chilean native plant extracts. © 2024, The Author(s).es_ES
dc.description.sponsorshipCIDI, (05/06); Centros de Investigación y Desarrollo, Universidad de Valparaíso, CID; Fondo Nacional de Desarrollo Científico y Tecnológico, FONDECYT, (1191763); Universidad de Valparaíso, UV, (CIDI (05/06)); Centro Interdisciplinario de Neurociencia de Valparaíso, Universidad de Valparaíso, CINV, UVes_ES
dc.language.isoenes_ES
dc.publisherBioMed Central Ltdes_ES
dc.subjectCancer cell lineses_ES
dc.subjectChilean native plantses_ES
dc.subjectRedox unbalancees_ES
dc.subjectSelective oxycutiones_ES
dc.titleOxidative stress promotes cytotoxicity in human cancer cell lines exposed to Escallonia spp. extractses_ES
dc.typeArticlees_ES


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