Iron Oxide Nanoparticles Conjugated to Thiosemicarbazone Reduce the Survival of Cancer Cells by Increasing the Gene Expression of in Lung Cancer A549 Cells.

BACKGROUND

Cancer cells have a higher demand for iron to grow and proliferate. A new complex of iron nanoparticles and thiosemicarbazones was synthesized. Confirmation tests included UV-visible, scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), Fourier transform infrared (FTIR), X-ray diffraction (XRD) and zeta potential.

METHODS

MTT assay, flow cytometry and qRT-PCR were used to investigate anti-proliferative effect, amount of apoptosis and the effect of Fe O @Glu/BTSC on changes in gene expression of (), respectively. The specifications of Fe O @ Glu/BTSC were confirmed at 5 nm.

RESULTS

Fe3O4@Glu/BTSC was more effective than BTSC and Fe O on A549 cells (IC=166.77 µg/mL) but its effect on healthy cells was smaller (CC=189.15 µg/mL). The drug selectivity index (SI) was calculated to be 1.13. The initial apoptosis rate was 46.33% for Fe O @Glu/BTSC, 28.27% for BTSC and 26.02% for Fe O . BTSC and BTSC@Fe O inhibited the cell cycle progression in the Sub-G1 and S phases. expression was 6.9 times higher in treated cells compared to the control group. The expression rate was 2.2 with BTSC compared to the control group and 1.6 times for Fe O.

CONCLUSION

Fe O @Glu/BTSC has proper anti-proliferative effects against lung cancer cells by increasing the expression of and inhibiting the cell cycle with the apoptosis activation pathway.