Apoptotic and cell cycle effects of triterpenes isolated from Phoradendron wattii on leukemia cell lines

Current antineoplastic agents present multiple disadvantages, driving an ongoing search for new and better compounds. Four lupane-type triterpenes, 3α,24-dihydroxylup-20(29)-en-28-oic acid (1), 3α,23-dihydroxy-30-oxo-lup-20(29)-en-28-oic acid (2), 3α,23-O-isopropylidenyl-3α,23-dihydroxylup-20(29)-en...

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Detalles Bibliográficos
Autores: LIA SARAHI VALENCIA CHAN, Dafné Linda Moreno Lorenzana, JIMMY JOSUE CEBALLOS CRUZ, SERGIO RUBEN PERAZA SANCHEZ, ANTONIETA CHAVEZ-GONZALEZ, ROSA MOO_PUC
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:México
Institución:Centro de Investigación Científica de Yucatán
Repositorio:Repositorio Institucional CICY
Idioma:inglés
OAI Identifier:oai:cicy.repositorioinstitucional.mx:1003/2257
Acceso en línea:http://cicy.repositorioinstitucional.mx/jspui/handle/1003/2257
Access Level:acceso abierto
Palabra clave:info:eu-repo/classification/Autores/LEUKEMIA
info:eu-repo/classification/Autores/LUPANE-TYPE TRITERPENE
info:eu-repo/classification/Autores/APOPTOSIS
info:eu-repo/classification/Autores/CELL CYCLE
info:eu-repo/classification/Autores/MOLECULAR DOCKING
info:eu-repo/classification/cti/2
info:eu-repo/classification/cti/24
info:eu-repo/classification/cti/2403
info:eu-repo/classification/cti/230221
Descripción
Sumario:Current antineoplastic agents present multiple disadvantages, driving an ongoing search for new and better compounds. Four lupane-type triterpenes, 3α,24-dihydroxylup-20(29)-en-28-oic acid (1), 3α,23-dihydroxy-30-oxo-lup-20(29)-en-28-oic acid (2), 3α,23-O-isopropylidenyl-3α,23-dihydroxylup-20(29)-en-28-oic acid (3), and 3α,23-dihydroxylup-20(29)-en-28-oic acid (4), previously isolated from Phoradendron wattii, were evaluated on two cell lines of chronic (K562) and acute (HL60) myeloid leukemia. Compounds 1, 2, and 4 decreased cell viability and inhibit proliferation, mainly in K562, and exhibited an apoptotic effect from 24 h of treatment. Of particular interest is compound 2, which caused arrest in active phases (G2/M) of the cell cycle, as shown by in silico study of the CDK1/Cyclin B/Csk2 complex by molecular docking. This compound [3α,23-dihydroxy-30-oxo-lup-20(29)-en-28-oic acid] s a promising candidate for incorporation into cancer treatments and deserves further study. © 2022 by the authors.