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In vitro anti-proliferative effect and in vivo antitumor action of daphnetin in different tumor cells.
Jiménez-Orozco, F Alejandro; Randelovic, Ivan; Hegedüs, Zita; Vega-Lopez, Armando; Martínez-Flores, Francisco; Tóvarí, József.
Afiliación
  • Jiménez-Orozco FA; Department of Pharmacology, School of Medicine, Universidad Nacional Autoinoma de Mexico, Mexico City, Mexico.
  • Randelovic I; Department of Experimental Pharmacology, National Institute of Oncology, Budapest, Hungary.
  • Hegedüs Z; Department of Experimental Pharmacology, National Institute of Oncology, Budapest, Hungary.
  • Vega-Lopez A; Environmental Toxicology Laboratory, Escuela Nacional de Ciencias Bioloigicas, Instituto Politécnico Nacional, Mexico City, Mexico.
  • Martínez-Flores F; Skin and Tissue Bank, Instituto Nacional de Rehabilitación, Secretaría de Salud, Mexico City, Mexico.
  • Tóvarí J; Department of Experimental Pharmacology, National Institute of Oncology, Budapest, Hungary.
Cir Cir ; 88(6): 765-771, 2020.
Article en En | MEDLINE | ID: mdl-33254179
RESUMEN
BACKGROUND: The anti-inflammatory effects of daphnetin (7,8-dihidroxicoumarin) have been well-documented, but the potential of daphnetin as an anticancer agent is controversial and remains insufficiently explored. MATERIAL AND METHODS: In this work, we evaluated the in vitro anti-proliferative effect of daphnetin in three cell lines by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assays, as well as its in vivo antitumor effect in four different types of mouse tumor. RESULTS: With a correlation between in vitro and in vivo results, the tested cell types have different sensitivity to the compound. The following cell lines are arranged according to the in vitro anti-proliferative potency of daphnetin: B16 melanoma cells (inhibitory concentrations 50 [IC50] = 54 ± 2.8 µM) > mitoxantrone (MXT) breast adenocarcinoma cells (IC50 = 74 ± 6.4 µM) > C26 colon carcinoma cells (IC50 = 108 ± 7.3 µM). In vivo, the optimal antitumor dose of daphnetin was 40 mg/kg and the magnitudes of inhibition were the following: B16 tumor (48%) > MXT tumor (40%) > S180 fibrosarcoma tumor (30%) > C26 tumor (20%). CONCLUSION: Our results indicate that daphnetin might have an impact as adjuvant to improve the effectiveness of conventional chemotherapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adenocarcinoma / Neoplasias del Colon Límite: Humans Idioma: En Revista: Cir Cir Año: 2020 Tipo del documento: Article País de afiliación: México Pais de publicación: México

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Adenocarcinoma / Neoplasias del Colon Límite: Humans Idioma: En Revista: Cir Cir Año: 2020 Tipo del documento: Article País de afiliación: México Pais de publicación: México