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Neoplastic cell response to tiopronin-coated gold nanoparticles

  • Lei Cui
  • , Payam Zahedi
  • , Justin Saraceno
  • , Robert Bristow
  • , David Jaffray
  • , Christine Allen*
  • *Corresponding author for this work
  • University of Toronto
  • Radiation Oncology and Medical Biophysics
  • Princess Margaret Hospital
  • University Health Network
  • STTARR Innovation Centre

Research output: Contribution to journal › Article › peer-review

Abstract

The present study characterized the in vitro biological response of a comprehensive set of cancer cell lines to gold nanoparticles (2.7 nm) coated with tiopronin (AuNPs-TP). Our findings suggest that upon entering cells, the AuNPs-TP are sequestered in vacuoles such as endosomes and lysosomes, and mostly localize in perinuclear areas. Peak cell accumulation was achieved at 8 hours after incubation. L929 and H520 cells showed more than 75% surviving fraction when treated with 0.5 mg/mL of AuNPs-TP for 24 hours, whereas the surviving fractions were 60% in MCF-7 and 20% in HeLa cells. Reactive oxygen species (ROS) production by the AuNPs-TP was dependent on cell line and exposure time. Antioxidants inhibited ROS generation to various extents, with glutathione and tiopronin being most effective. Overall, exposure time, concentration of the AuNPs-TP, and cell line influenced neoplastic cell response. Furthermore, the mechanism of cytotoxicity of the AuNPs-TP was found to be ROS generation. From the Clinical Editor: This study describes the basic intracellular characteristics of Tiopronin-Au nanoparticles from the standpoint of their anti-cancer activity in different cancer cell cultures.

Original languageEnglish
Pages (from-to)264-273
Number of pages10
JournalNanomedicine: Nanotechnology, Biology, and Medicine
Volume9
Issue number2
DOIs
Publication statusPublished - Feb 2013

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cancer
  • Cellular accumulation
  • Cytotoxicity
  • Gold nanoparticles
  • Reactive oxygen species

Research Highlights, Institutes and Platforms

  • Manchester Cancer Research Centre

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