Glucose capped silver nanoparticles induce cell cycle arrest in HeLa cells

Toxicol In Vitro. 2017 Jun:41:64-74. doi: 10.1016/j.tiv.2017.02.014. Epub 2017 Feb 20.

Abstract

This study aims to determine the interaction (uptake and biological effects on cell viability and cell cycle progression) of glucose capped silver nanoparticles (AgNPs-G) on human epithelioid cervix carcinoma (HeLa) cells, in relation to amount, 2×103 or 2×104 NPs/cell, and exposure time, up to 48h. The spherical and well dispersed AgNPs (30±5nm) were obtained by using glucose as reducing agent in a green synthesis method that ensures to stabilize AgNPs avoiding cytotoxic soluble silver ions Ag+ release. HeLa cells take up abundantly and rapidly AgNPs-G resulting toxic to cells in amount and incubation time dependent manner. HeLa cells were arrested at S and G2/M phases of the cell cycle and subG1 population increased when incubated with 2×104 AgNPs-G/cell. Mitotic index decreased accordingly. The dissolution experiments demonstrated that the observed effects were due only to AgNPs-G since glucose capping prevents Ag+ release. The AgNPs-G influence on HeLa cells viability and cell cycle progression suggest that AgNPs-G, alone or in combination with chemotherapeutics, may be exploited for the development of novel antiproliferative treatment in cancer therapy. However, the possible influence of the cell cycle on cellular uptake of AgNPs-G and the mechanism of AgNPs entry in cells need further investigation.

Keywords: Cell cycle; Cytotoxicity; HeLa cells; Nanoparticles uptake; Silver nanoparticles (AgNPs).

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Cell Cycle Checkpoints / drug effects*
  • Cell Survival / drug effects
  • Glucose / pharmacology*
  • HeLa Cells
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Metal Nanoparticles* / ultrastructure
  • Microscopy, Electron, Transmission
  • Silver / pharmacology*

Substances

  • Antineoplastic Agents
  • Silver
  • L-Lactate Dehydrogenase
  • Glucose