Anisotropic gold nanoparticles have been prepared by the photochemical reduction in the room-temperature
ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF4]) without any additional capping
agent. Scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy,
X-ray diffraction, and Fourier transform infrared spectroscopy have been used to characterize the as-prepared
products. The results show that especial shape gold particles can be controlled by [BMIM][BF4] and reaction
conditions such as reaction time and reagent concentration. The [BMIM][BF4] is a reaction medium, template,
and capping agent. Under different reaction conditions, various morphologies such as sheet (triangle and
hexagon) polyhedron of gold nanoparticles can be obtained. The mechanisms of photochemical reduction
reaction and controlled growth of gold nanoparticles have also been discussed.
Cancer side-population (SP) represents a sub-population of stem-like cancer cells that have an important role in drug resistance due to their high expression of the ATP-binding cassette transporter ABCG2 involved in drug export. Auranofin (AF), a clinical drug of gold complex that is used in treatment of rheumatoid arthritis, has been reported inducing tumor antiproliferation. However, whether AF can impact SP cells remains unclear. Our study showed that AF caused a depletion of SP cells and a downregulation of stem cell markers, and impaired their ability to form tumor colonies in vitro and incidence to develop tumors in vivo of lung cancer cells. Reactive oxygen species (ROS) had an important role in mediating AF-induced depletion of SP cells, which could be reversed by antioxidant NAC. Further study revealed that AF could also cause ATP depletion by inhibition of glycolysis. The depletion of cellular ATP might impair the function of ABCG2 pump, leading to increased drug accumulation within the cells and thus enhancing anticancer activity of chemotherapeutic agents such as adriamycin. Synergistic effect of AF and adriamycin was demonstrated both in vitro and in vivo. Simultaneous increase of ROS and inhibition of glycolysis is a novel strategy to eliminate stem-like cancer cells. Combination of AF with adriamycin seems to be promising to enhance therapeutic effectiveness.
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