N

Alice Dassano, Mariateresa Mancuso, Paola Giardullo, Loris De Cecco, Pierangela Ciuffreda, Enzo Santaniello, Anna Saran, Tommaso A. Dragani, Francesca Colombo

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

N6-isopentenyladenosine (i6A), a naturally occurring modified nucleoside, inhibits the proliferation of human tumor cell lines in vitro, but its mechanism of action remains unclear. Treatment of MCF7 human breast adenocarcinoma cells with i6A or with three synthetic analogs (allyl6A, benzyl6A, and butyl6A) inhibited growth and altered gene expression. About 60% of the genes that were differentially expressed in response to i6A treatment were also modulated by the analogs, and pathway enrichment analysis identified the NRF2-mediated oxidative stress response as being significantly modulated by all four compounds. Luciferase reporter gene assays in transfected MCF7 cells confirmed that i6A activates the transcription factor NRF2. Assays for cellular production of reactive oxygen species indicated that i6A and analogs had antioxidant effects, reducing basal levels and inhibiting the H2O2- or 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced production in MCF7 or dHL-60 (HL-60 cells induced to differentiate along the neutrophilic lineage) cell lines, respectively. In vivo, topical application of i6A or benzyl6A to mouse ears prior to TPA stimulation lessened the inflammatory response and significantly reduced the number of infiltrating neutrophils. These results suggest that i6A and analogs trigger a cellular response against oxidative stress and open the possibility of i6A and benzyl6A being used as topical anti-inflammatory drugs. © 2014 The Authors.
Original languageEnglish
Pages (from-to)580 - 589
Number of pages10
JournalRedox Biology
Volume2
Issue number1
DOIs
Publication statusPublished - 2014
Externally publishedYes

    Fingerprint

All Science Journal Classification (ASJC) codes

  • Organic Chemistry
  • Clinical Biochemistry

Cite this

Dassano, A., Mancuso, M., Giardullo, P., Cecco, L. D., Ciuffreda, P., Santaniello, E., Saran, A., Dragani, T. A., & Colombo, F. (2014). N. Redox Biology, 2(1), 580 - 589. https://doi.org/10.1016/j.redox.2014.03.001