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Purinergic signaling as potential target of thiamethoxam-induced neurotoxicity using silver catfish (Rhamdia quelen) as experimental model
Authors:Matheus D. Baldissera  Carine F. Souza  Jaqueline I. Golombieski  Débora Seben  Letícia R. Sippert  Joseânia Salbego  Enio Marchesan  Renato Zanella  Bernardo Baldisserotto
Affiliation:1.Graduate School of Humanity-Oriented Science and Engineering,Kindai University,Iizuka,Japan;2.Department of Biological and Environmental Chemistry, Faculty of Humanity-Oriented Science and Engineering,Kindai University,Iizuka,Japan;3.Technology Development Section,UHA Mikakuto Co., Ltd,Chuo-ku,Japan;4.Department of Cell Biology, Faculty of Medicine,Fukuoka University,Jonan-ku,Japan;5.Central Research Institute for Advanced Molecular Medicine,Fukuoka University,Jonan-ku,Japan
Abstract:Resveratrol is a polyphenolic compound in many edible foods including grapes, peanuts, and berries. Several studies have revealed the beneficial effects of resveratrol against various diseases such as heart disease, diabetes, obesity, neurological disorders, and cancer. A recent study showed that resveratrol inhibits the proliferation of HCT116 human colorectal cancer cells in three-dimensional culture (3DC) via induction of luminal apoptosis in HCT116 cell spheroids. In this study, we showed that a novel compound, caffeic acid-adducted resveratrol, has a stronger inhibitory effect on the growth of HCT116 cell spheroids in 3DC than resveratrol. It showed almost the same inhibitory efficacy as 5-fluorouracil, a conventional anticancer drug. We further showed that the resveratrol derivative did not affect the growth of HKe3 cell spheroids derived from HCT116 cells by disruption of the activating mutant KRAS gene. These results suggest that the resveratrol derivative inhibits the growth of HCT116 cell spheroids via inhibition of an oncogenic KRAS-mediated signaling pathway.
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