Inhibitory effect of silver nanoparticles on proliferation of estrogen-dependent MCF-7/BUS human breast cancer cells induced by butyl paraben or di-n-butyl phthalate

Toxicol Appl Pharmacol. 2017 Dec 15:337:12-21. doi: 10.1016/j.taap.2017.10.014. Epub 2017 Oct 23.

Abstract

In this study the effect of silver nanoparticles (AgNPs) on proliferation of estrogen receptor (ER)-positive human breast cancer MCF-7/BUS cells was assessed by means of in vitro assay. The cells were exposed in the absence of estrogens to AgNPs alone or in combination with aluminum chloride (AlCl3), butyl paraben (BPB) and di-n-butyl phthalate (DBPh). The results revealed that AgNPs at the non-cytotoxic concentrations (up to 2μg/mL) and AlCl3 (up to 500μM) did not induce proliferation of MCF-7/BUS cells whereas BPB and DBPh showed strong estrogenic activity with the highest effect at 16μM and 35μM, respectively. AgNPs inhibited the proliferation of the cells induced by DBPh, BPB or even with 17β-estradiol (E2) during 6-day incubation in the absence of estrogens. ICI 182,780 (10nM), a known estrogen receptor (ER) antagonist, induced strong inhibitory effect. AgNPs also decreased transcription of the estrogen-responsive pS2 and progesterone receptor (PGR) genes but modulated expression neither of ERα nor ERβ in MCF-7/BUS cells exposed to BPB, DBPh or E2 for 6h. Our results indicate that AgNPs may inhibit growth of breast cancer cells stimulated by E2 or estrogenic chemicals, i.e. BPB and DBPh.

Keywords: Aluminum; Breast cancer cells; Estrogenic activity; Paraben; Phthalate; Silver nanoparticles.

MeSH terms

  • Aluminum Chloride
  • Aluminum Compounds / pharmacology
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cell Proliferation / drug effects*
  • Chlorides / pharmacology
  • Dibutyl Phthalate / toxicity*
  • Dose-Response Relationship, Drug
  • Estradiol / toxicity*
  • Estrogen Antagonists / pharmacology
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / metabolism
  • Estrogen Receptor beta / genetics
  • Estrogen Receptor beta / metabolism
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • MCF-7 Cells
  • Metal Nanoparticles*
  • Parabens / toxicity*
  • Receptors, Progesterone / genetics
  • Receptors, Progesterone / metabolism
  • Silver Compounds / pharmacology*
  • Silver Compounds / toxicity
  • Transcription, Genetic / drug effects
  • Trefoil Factor-1 / genetics
  • Trefoil Factor-1 / metabolism

Substances

  • Aluminum Compounds
  • Chlorides
  • ESR1 protein, human
  • ESR2 protein, human
  • Estrogen Antagonists
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Parabens
  • Receptors, Progesterone
  • Silver Compounds
  • TFF1 protein, human
  • Trefoil Factor-1
  • Dibutyl Phthalate
  • Aluminum Chloride
  • Estradiol