典型文献
Investigation and experimental validation of curcumin-related mechanisms against hepatocellular carcinoma based on network pharmacology
文献摘要:
Objective: To determine the potential molecular mechanisms underlying the therapeutic effect of curcumin on hepatocellular carcinoma (HCC) by network pharmacology and experimental in vitro validation. Methods: The predictive targets of curcumin or HCC were collected from several databases. the identified overlapping targets were crossed with Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses using the Database for Annotation, Visualization, and Integrated Discovery (DAVID) platform. Two of the candidate pathways were selected to conduct an experimental verification. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide tetrazolium (MTT) assay was used to determine the effect of curcumin on the viability of HepG2 and LO2 cells. The apoptosis and autophagy of HepG2 cells were respectively detected by flow cytometry and transmission electron microscopy. Besides, western blot and real-time polymerase chain reaction (PCR) were employed to verify the p53 apoptotic pathway and adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) autophagy pathway. HepG2 cells were pretreated with pifithrin-α (PFT-α) and GSK690693 for further investigation. Results: The 167 pathways analyzed by KEGG included apoptosis, autophagy, p53, and AMPK pathways. The GO enrichment analysis demonstrated that curcumin was involved in cellular response to drug, regulation of apoptotic pathway, and so on. The in vitro experiments also confirmed that curcumin can inhibit the growth of HepG2 cells by promoting the apoptosis of p53 pathway and autophagy through the AMPK pathway. Furthermore, the protein and messenger RNA (mRNA) of the two pathways were downregulated in the inhibitor-pretreated group compared with the experimental group. The damage-regulated autophagy modulator (DRAM) in the PFT-α-pretreated group was downregulated, and p62 in the GSK690693-pretreated group was upregulated. Conclusions:Curcumin can treat HCC through the p53 apoptotic pathway and the AMPK/Unc-51-like kinase 1 (ULK1) autophagy pathway, in which the mutual transformation of autophagy and apoptosis may occur through DRAM and p62.
文献关键词:
中图分类号:
作者姓名:
Yang CHEN;Qian LI;Sisi REN;Ting CHEN;Bingtao ZHAI;Jiangxue CHENG;Xiaoyan SHI;Liang SONG;Yu FAN;Dongyan GUO
作者机构:
College of Basic Medicine,Shaanxi University of Chinese Medicine,Xianyang 712046,China;School of Pharmacy,Shaanxi University of Chinese Medicine,Xianyang 712046,China;Medical Experimental Center,Shaanxi University of Chinese Medicine,Xianyang 712046,China;Shaanxi Provincial Key Laboratory of TCM Constitution and Disease Prevention,Shaanxi University of Chinese Medicine,Xianyang 712046,China
引用格式:
[1]Yang CHEN;Qian LI;Sisi REN;Ting CHEN;Bingtao ZHAI;Jiangxue CHENG;Xiaoyan SHI;Liang SONG;Yu FAN;Dongyan GUO-.Investigation and experimental validation of curcumin-related mechanisms against hepatocellular carcinoma based on network pharmacology)[J].浙江大学学报(英文版)(B辑:生物医学和生物技术),2022(08):682-698
A类:
pifithrin,GSK690693
B类:
Investigation,experimental,validation,curcumin,related,mechanisms,against,hepatocellular,carcinoma,network,pharmacology,Objective,To,determine,potential,molecular,underlying,therapeutic,effect,HCC,by,vitro,Methods,predictive,targets,were,collected,from,several,databases,identified,overlapping,crossed,Ontology,Kyoto,Encyclopedia,Genes,Genomes,analyses,using,Database,Annotation,Visualization,Integrated,Discovery,DAVID,platform,Two,candidate,pathways,selected,conduct,verification,dimethylthiazol,diphenyltetrazolium,bromide,MTT,assay,was,used,viability,HepG2,LO2,cells,apoptosis,autophagy,respectively,detected,flow,cytometry,transmission,electron,microscopy,Besides,western,blot,real,polymerase,chain,reaction,employed,verify,p53,apoptotic,adenosine,monophosphate,activated,protein,kinase,AMPK,pretreated,PFT,further,investigation,Results,analyzed,included,enrichment,analysis,demonstrated,that,involved,response,drug,regulation,experiments,also,confirmed,growth,promoting,through,Furthermore,messenger,downregulated,inhibitor,group,compared,damage,modulator,DRAM,p62,upregulated,Conclusions,Curcumin,Unc,like,ULK1,which,mutual,transformation,may,occur
AB值:
0.488793
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