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Int J Oncol ; 56(1): 390-397, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31814036

RESUMEN

8­Gingerol, which is extracted from ginger (Zingiber officinale Roscoe), has been shown to possess antioxidant and anti­inflammatory properties. However, the antitumor effect of 8­gingerol has not been fully elucidated. The aim of the present study was to investigate the therapeutic potential of 8­gingerol against colorectal cancer (CRC). The results demonstrated that 8­gingerol significantly inhibited cell proliferation in CRC cell models. Treatment of CRC cells with 8­gingerol resulted in dose­dependent decreases in migration and invasion. The inhibitory effect of 8­gingerol on CRC cell growth was attributed to cell cycle arrest and increased apoptosis. Moreover, to the best of our knowledge, the present study was the first to demonstrate that 8­gingerol acted as an inhibitor of epidermal growth factor receptor (EGFR) signaling. 8­Gingerol inhibited CRC cell proliferation and migration by targeting the EGFR/signal transducer and activator of transcription/extracellular signal­regulated kinase pathway, and the effects of 8­gingerol depended on the expression of EGFR. Moreover, 8­gingerol reduced the effective dosage of 5­fluorouracil and, thereby, the toxicity of drug combination therapy. These data suggest that 8­gingerol may be a promising candidate for the development of novel anticancer agents against CRC.


Asunto(s)
Catecoles/farmacología , Movimiento Celular , Proliferación Celular , Neoplasias Colorrectales/patología , Alcoholes Grasos/farmacología , Proteína Quinasa 1 Activada por Mitógenos/metabolismo , Proteína Quinasa 3 Activada por Mitógenos/metabolismo , Factor de Transcripción STAT3/metabolismo , Apoptosis , Biomarcadores de Tumor/genética , Biomarcadores de Tumor/metabolismo , Ciclo Celular , Neoplasias Colorrectales/tratamiento farmacológico , Neoplasias Colorrectales/metabolismo , Receptores ErbB/genética , Receptores ErbB/metabolismo , Regulación Neoplásica de la Expresión Génica , Humanos , Proteína Quinasa 1 Activada por Mitógenos/genética , Proteína Quinasa 3 Activada por Mitógenos/genética , Factor de Transcripción STAT3/genética , Células Tumorales Cultivadas
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