研究目的
To explore new therapies for castration-resistant prostate cancer (CRPC) to improve patients’ quality of life and extend life.
研究成果
CuS nanoplates are characterized by simple preparation, low biotoxicity and high photothermal conversion efficiency. 980 nm NIR-light-driven CuS nanoplates can significantly inhibit the progression of prostate cancer. Regulating autophagy can enhance the efficacy of CuS nanoplates photothermal therapy in the treatment of prostate cancer.
研究不足
The lack of a targeted approach for small numbers of cells to uptake the nanoplates and then be heated is a major limitation of the clinical application of the work presented.
1:Experimental Design and Method Selection:
The study involved the synthesis of CuS nanoplates, their characterization, and the evaluation of their photothermal conversion efficiency.
2:Sample Selection and Data Sources:
Prostate cancer cells (PC-3 and DU145) and normal human prostate epithelial cells (RWPE-1) were used.
3:List of Experimental Equipment and Materials:
CuS nanoplates, near-infrared (NIR) light source, transmission electron microscope, mCherry-LC3 syncytial virus, acridine orange staining, and autophagy protein detection tools.
4:Experimental Procedures and Operational Workflow:
Cells were cultured with CuS nanoplates, exposed to NIR light, and analyzed for viability, autophagy, and necrosis.
5:Data Analysis Methods:
Statistical analysis was performed using SPSS 22.0 and Graph Pad Prism 5.0 software.
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