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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/47003

    Título
    Natural triterpenic diols promote apoptosis in astrocytoma cells through ROS-mediated mitochondrial depolarization and JNK activation
    Autor
    Martín Martín, Rubén
    Ibeas, Elvira
    Carvalho Tavares, Juliana
    Hernández Garrido, MaritaAutoridad UVA Orcid
    Ruiz Gutierrez, Valentina
    Nieto Callejo, María Luisa
    Año del Documento
    2009
    Editorial
    PLOS ONE
    Descripción
    Producción Científica
    Documento Fuente
    PLoS ONE, 2009, vol. 4, n. 6. 14 p.
    Resumo
    Background: Triterpene alcohols and acids are multifunctional compounds widely distributed throughout the plant kingdom that exhibit a variety of beneficial health properties, being synthetic analogs of oleanolic acid under clinical evaluation as anti-tumoral therapeutic agents. However, the antineoplastic activity of two natural occuring triterpenoid alcohols extracted from olive oil, erythrodiol (an intermediate from oleanolic acid), and its isomer, uvaol, has barely been reported, particularly on brain cancer cells. Astrocytomas are among the most common and aggressive type of primary malignant tumors in the neurological system lacking effective treatments, and in this study, we addressed the effect of these two triterpenic diols on the human 1321N1 astrocytoma cell line. Principal Findings: Erythrodiol and uvaol effectively affected cell proliferation, as well as cell cycle phases and induced 1321N1 cell death. Both triterpenes successfully modulated the apoptotic response, promoting nuclear condensation and fragmentation. They caused retraction and rounding of cultured cells, which lost adherence from their supports, while F-actin and vimentin filaments disappeared as an organized cytoplasmic network. At molecular level, changes in the expression of surface proteins associated with adhesion or death processes were also observed. Moreover, triterpene exposure resulted in the production of reactive oxygen species (ROS) with loss of mitochondrial transmembrane potential, and correlated with the activation of c-Jun N-terminal kinases (JNK). The presence of catalase reversed the triterpenic diols-induced mitochondrial depolarization, JNK activation, and apoptotic death, indicating the critical role of ROS in the action of these compounds. Conclusions: Overall, we provide a significant insight into the anticarcinogenic action of erythrodiol and uvaol that may have a potential in prevention and treatment of brain tumors and other cancers.
    Palabras Clave
    Triterpenic diols
    Dioles triterpénicos
    Apoptosis
    Astrocytoma cells
    Astrocitomas
    Mitochondrial depolarization
    Despolarización mitocondrial
    ISSN
    1932-6203
    Revisión por pares
    SI
    DOI
    10.1371/journal.pone.0005975
    Patrocinador
    Ministerio de Ciencia e Innovación (grants SAF2005-01242, SAF2008-00245 and AGL2008-022845)
    Junta de Castilla y León (grant CSI11A08)
    Version del Editor
    https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0005975
    Propietario de los Derechos
    © 2009 PLOS
    Idioma
    eng
    URI
    https://uvadoc.uva.es/handle/10324/47003
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
    Aparece en las colecciones
    • DEP06 - Artículos de revista [352]
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    Attribution-NonCommercial-NoDerivatives 4.0 InternacionalExceto quando indicado o contrário, a licença deste item é descrito como Attribution-NonCommercial-NoDerivatives 4.0 Internacional

    Universidad de Valladolid

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