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作 者:Yanping Gao Zhiyong Dong Jun Bai
机构地区:[1]Department of Gynecology,The First People's Hospital of Datong(Women and Children’s Hospital of Shanxi Datong University),Datong 037000,China [2]Department of Gynecology,The First Affiliated Hospital of Jinan University,Guangzhou 510630,China [3]Institute of Oncology,Shanxi Datong University,Datong 037000,China
出 处:《Oncology and Translational Medicine》2022年第6期285-292,共8页肿瘤学与转化医学(英文版)
基 金:Supported by a grant from the Scientific Research Project of Shanxi Provincial Health Commission(No.2021166)。
摘 要:Objective To investigate the anticancer effect of a novel derivative of genistein(5-hydroxy-4’-nitro-7-propionyloxy-genistein,HNPG)on human ovarian cancer HO-8910 cells and its possible molecular mechanism.Methods HO-8910 cells were cultured in vitro,and the inhibitory effect of HNPG on proliferation was determined using MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide]assay.The effect of HNPG on inducing apoptosis was examined using FCM with Annexin V-FITC and propidium iodide staining.The effect of HNPG on regulating reactive oxygen species(ROS)was measured using FCM with 2’,7’-di chlorodihydro-fluorescein diacetate staining.The effect of HNPG on modulating mitochondrial membrane potential(MMP)was determined using FCM with lipophilic cationic dye 2(6 Amino 3 imino 3H xanthen 9 yl)benzoic acid methyl ester(Rh123)staining.The bioactivity of superoxide dismutase(SOD)and catalase(CAT)and the content of glutathione(GSH)and malondialdehyde(MDA)were detected using enzymelinked immunosorbent assay.The related apoptotic proteins,including bcl-2,bax,cyt-c,and cleavedcaspase-3,were assessed using western blotting.Results HNPG exhibited dramatic antitumor activity against HO-8910 cells in vitro,inhibited proliferation,and induced apoptosis in a time-and dose-dependent manner.These effects were accompanied by reduced bioactivity of SOD and CAT,reduced GSH content,and enhanced MDA content.Simultaneously,the amount of ROS was increased and the level of MMP was reduced,along with upregulation of mitochondrial apoptosis pathway-related proteins,bax,cyt-c,and cleaved-caspase-3;bcl-2 protein was downregulated.Conclusion HNPG inhibited proliferation of human ovarian cancer HO-8910 cells in vitro,which might be related to decreased bioactivity of SOD and CAT.HNPG also reduced GSH content,which resulted in ROS accumulation in cells,damaged the integrity of mitochondrial membrane,and induced cell apoptosis.
关 键 词:ovarian cancer 5-hydroxy-4’-nitro-7-propionyloxy-genistein reactive oxygen species PROLIFERATION apoptosis
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