Silver nanoparticles selectively treat triple‐negative breast cancer cells without affecting non‐malignant breast epithelial cells in vitro and in vivo

• Published in: FASEB bioAdvances Vol. 1; no. 10; pp. 639 - 660
• Main Authors: Swanner, Jessica, Fahrenholtz, Cale D., Tenvooren, Iliana, Bernish, Brian W., Sears, James J., Hooker, Allison, Furdui, Cristina M., Alli, Elizabeth, Li, Wencheng, Donati, George L., Cook, Katherine L., Vidi, Pierre‐Alexandre, Singh, Ravi
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.10.2019; John Wiley and Sons Inc; Wiley
• Subjects: Antioxidants; Apoptosis; Breast cancer; Cancer therapies; Cell culture; Cytotoxicity; Deoxyribonucleic acid; DNA; DNA damage; Drug development; Endoplasmic reticulum; Epidermal growth factor; Epithelial cells; Insulin; Kinases; nanomedicine; Nanoparticles; Nodules; Penicillin; Proteins; redox; Silver; Structure-function relationships; toxicity; Tumors; unfolded protein response; Xenografts; toxicity; unfolded protein response; nanomedicine; DNA damage; redox
• ISSN: 2573-9832; 2573-9832
• DOI: 10.1096/fba.2019-00021

Silver nanoparticles (AgNPs) show promise for treatment of aggressive cancers including triple‐negative breast cancer (TNBC) in preclinical cancer models. For clinical development of AgNP‐based therapeutics, it will be necessary to clearly define the specific physicochemical features of the nanoparticles that will be used, and to tie these properties to biological outcomes. To fill this knowledge gap, we performed thorough structure/function, mechanistic, safety, and efficacy studies to assess the potential for AgNPs to treat TNBC. We establish that AgNPs, regardless of size, shape, or stabilizing agent, are highly cytotoxic to TNBC cells at doses that are not cytotoxic to non‐malignant breast epithelial cells. In contrast, TNBC cells and non‐malignant breast epithelial cells are similarly sensitive to exposure to silver cation (Ag+), indicating that the nanoparticle formulation is essential for the TNBC‐specific cytotoxicity. Mechanistically, AgNPs are internalized by both TNBC and non‐malignant breast cells, but are rapidly degraded only in TNBC cells. Exposure to AgNPs depletes cellular antioxidants and causes endoplasmic reticulum stress in TNBC cells without causing similar damage in non‐malignant breast epithelial cells. AgNPs also cause extensive DNA damage in 3D TNBC tumor nodules in vitro, but do not disrupt the normal architecture of breast acini in 3D cell culture, nor cause DNA damage or induce apoptosis in these structures. Lastly, we show that systemically administered AgNPs are effective at non‐toxic doses for reducing the growth of TNBC tumor xenografts in mice. This work provides a rationale for development of AgNPs as a safe and specific TNBC treatment.