Basic Study
Copyright ©The Author(s) 2023.
World J Hepatol. Mar 27, 2023; 15(3): 393-409
Published online Mar 27, 2023. doi: 10.4254/wjh.v15.i3.393
Figure 1
Figure 1 Cytotoxicity evaluation of Catharanthusroseus-silver nanoparticles on HepG2 and THLE-3 cells. A: The cytotoxicity of HepG2 cell lines treated with different concentrations of Catharanthus roseus-silver nanoparticles (C. roseus-AgNPs); B: The IC50 of C. roseus-AgNPs on HepG2 cells; C: The cytotoxicity of THLE3 cell lines treated with different concentrations of C. roseus-AgNPs; D: The IC50 of C. roseus-AgNPs on THLE-3 cells. All experiments were done in triplicate, and the data represent means ± standard deviations. The comparison between each concentration with untreated cells was done using two-way ANOVA with Dunnet post-test to detect any significant differences (bP < 0.01; cP < 0.001; ns not significant). C. roseus-AgNPs: Catharanthus roseus-silver nanoparticles.
Figure 2
Figure 2 The correlation analysis between samples. The colour represents the correlation coefficient.
Figure 3
Figure 3 Volcano plot of differentially expression genes. Red points represent upregulated differentially expression genes (DEGs). Blue points represent down-regulated DEGs. Grey points represent non-DEGs. DEGs: Differentially expression genes.
Figure 4
Figure 4  Gene Ontology classification of upregulated and downregulated differentially expression genes.
Figure 5
Figure 5 Network enrichment result. The darker the colour indicates the highest enrichment pathways. The larger the area, the higher the degree of enrichment.
Figure 6
Figure 6 Model of cytotoxicity mechanism in HepG2 cell treated with C. roseus-AgNPs that involves the upregulated genes (in red) and downregulated genes (in green).