Research Article

Isorhamnetin Induces Melanoma Cell Apoptosis via the PI3K/Akt and NF-κB Pathways

Figure 1

Effect of isorhamnetin on B16F10 cell proliferation. (a) Cells were treated with 0-100 μmol/L IH for 48 h and 72 h. CCK-8 assay showed that cell viability was dose-dependently reduced. (b) After treated with 0-100 μmol/L IH for 24 h, cells were incubated for an additional 7 days, then fixed with 3.7% paraformaldehyde, and stained with the crystal violet solution. The clonogenic assay indicated a suppressive effect of IH on B16F10 cells forming colonies. Each experiment was done at least three times. compared with control; compared with control.
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