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Ag/Au Bimetallic Nanoparticles Inhibit Tumor Growth and Prevent Metastasis in a Mouse Model
Hector Katifelis1, Iuliia Mukha2, Penelope Bouziotis3
1Laboratory of Biology, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
International Journal of Nanomedicine
|August 28, 2020
Summary
Silver-gold-tryptophan nanoparticles (Ag3Au1Trp1:2NPs) demonstrated significant antitumor and antimetastatic effects in a mouse cancer model. These nanoparticles selectively induce cancer cell apoptosis via the TRAIL-dependent pathway.
Area of Science:
- Nanomedicine
- Cancer Research
- Molecular Biology
Background:
- Nanoparticles (NPs) offer novel therapeutic strategies for cancer treatment.
- Targeted delivery of therapeutic agents to tumors is crucial for efficacy and minimizing side effects.
Purpose of the Study:
- To evaluate the antitumor and antimetastatic efficacy of silver-gold-tryptophan nanoparticles (Ag3Au1Trp1:2NPs) in a SCID mouse cancer model.
- To investigate the molecular mechanisms underlying the observed therapeutic effects.
Main Methods:
- Ag3Au1Trp1:2NPs were radiolabeled with Gallium-68 for biodistribution studies.
- Tumor growth was monitored, and metastatic potential was assessed in lung and liver tissues.
- Caspase-3 and TRAIL expression levels were analyzed using real-time PCR and Western blot.
Main Results:
- Ag3Au1Trp1:2NPs exhibited rapid accumulation at tumor sites.
- The highest dose of Ag3Au1Trp1:2NPs reduced tumor volume by 1.9-fold compared to controls.
- NPs treatment inhibited metastasis to the liver and lungs and increased Caspase-3 and TRAIL levels.
Conclusions:
- Ag3Au1Trp1:2NPs possess significant in vivo antitumor and antimetastatic properties.
- The nanoparticles induce cancer cell apoptosis through the extrinsic TRAIL-dependent pathway.
- Enhanced tumor targeting and retention contribute to the observed therapeutic effects.

