Background:
Hepatocellular carcinoma is the second leading cause of cancer-related
deaths among other types of cancer due to lack of effective treatments and late diagnosis. Nanocarriers
represent a novel method to deliver chemotherapeutic drugs, enhancing their bioavailability
and stability.
Methods:
In the present study, we loaded gold nanoparticles (AuNPs) and titanium oxide
nanoparticles (TiO2NPs) with ERL to investigate the efficiency of the formed composite in inducing
apoptosis in HepG2 liver cancer cells. Cytotoxicity was assessed using MTT assay and cell
phase distribution was assessed by flow cytometry along with apoptosis detection.
Results:
Data obtained indicated the efficiency of the formed composite to significantly induce
cell death and arrest cell cycle and G2/M phase. IRF4 was downregulated after treatment with
loaded ERL.
Conclusion:
Our data showed that loading ERL on TiO2NPs was more efficient than AuNPs.
However, both nanocarriers were efficient compared with control.
Methionine Adenosyltransferase 2B, HuR, and Sirtuin 1 Protein Cross-talk Impacts on the Effect of Resveratrol on Apoptosis and Growth in Liver Cancer Cells
