Silver nanoparticles selectively treat triple‐negative breast cancer cells without affecting non‐malignant breast epithelial cells in vitro and in vivo. Issue 10 (30th September 2019)

• Record Type: Journal Article
• 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
• Is Part Of: FASEB bioAdvances. Volume 1:Issue 10(2019)
• Page Start: 639
• Page End: 660
• Publication Date: 2019-09-30
• Subjects: DNA damage -- nanomedicine -- redox -- toxicity -- unfolded protein response
• DOI: 10.1096/fba.2019-00021
• Languages: English
• ISSNs: 2573-9832

Abstract

Abstract: 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.