Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.

Both the methylxanthine caffeine and the heavy subunit of ferritin molecule (FHC) are able to control the proliferation rate of several cancer cell lines. While caffeine acts exclusively as a negative modulator of cell proliferation, FHC might reduce or enhance cell viability depending upon the diff...

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Main Authors: Fabiana Zolea, Flavia Biamonte, Anna Martina Battaglia, Maria Concetta Faniello, Giovanni Cuda, Francesco Costanzo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5033359?pdf=render
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spelling doaj-7e56251ac4304e6fa4a92604eab91a442020-11-24T21:35:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01119e016307810.1371/journal.pone.0163078Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.Fabiana ZoleaFlavia BiamonteAnna Martina BattagliaMaria Concetta FanielloGiovanni CudaFrancesco CostanzoBoth the methylxanthine caffeine and the heavy subunit of ferritin molecule (FHC) are able to control the proliferation rate of several cancer cell lines. While caffeine acts exclusively as a negative modulator of cell proliferation, FHC might reduce or enhance cell viability depending upon the different cell type. In this work we have demonstrated that physiological concentrations of caffeine reduce the proliferation rate of H460 cells: along with the modulation of p53, pAKT and Cyclin D1, caffeine also determines a significant FHC up-regulation through the activation of its transcriptional efficiency. FHC plays a central role in the molecular pathways modulated by caffeine, ending in a reduced cell growth, since its specific silencing by siRNA almost completely abolishes caffeine effects on H460 cell proliferation. These results allow the inclusion of ferritin heavy subunits among the multiple molecular targets of caffeine and open the way for studying the relationship between caffeine and intracellular iron metabolism.http://europepmc.org/articles/PMC5033359?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Fabiana Zolea
Flavia Biamonte
Anna Martina Battaglia
Maria Concetta Faniello
Giovanni Cuda
Francesco Costanzo
spellingShingle Fabiana Zolea
Flavia Biamonte
Anna Martina Battaglia
Maria Concetta Faniello
Giovanni Cuda
Francesco Costanzo
Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.
PLoS ONE
author_facet Fabiana Zolea
Flavia Biamonte
Anna Martina Battaglia
Maria Concetta Faniello
Giovanni Cuda
Francesco Costanzo
author_sort Fabiana Zolea
title Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.
title_short Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.
title_full Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.
title_fullStr Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.
title_full_unstemmed Caffeine Positively Modulates Ferritin Heavy Chain Expression in H460 Cells: Effects on Cell Proliferation.
title_sort caffeine positively modulates ferritin heavy chain expression in h460 cells: effects on cell proliferation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Both the methylxanthine caffeine and the heavy subunit of ferritin molecule (FHC) are able to control the proliferation rate of several cancer cell lines. While caffeine acts exclusively as a negative modulator of cell proliferation, FHC might reduce or enhance cell viability depending upon the different cell type. In this work we have demonstrated that physiological concentrations of caffeine reduce the proliferation rate of H460 cells: along with the modulation of p53, pAKT and Cyclin D1, caffeine also determines a significant FHC up-regulation through the activation of its transcriptional efficiency. FHC plays a central role in the molecular pathways modulated by caffeine, ending in a reduced cell growth, since its specific silencing by siRNA almost completely abolishes caffeine effects on H460 cell proliferation. These results allow the inclusion of ferritin heavy subunits among the multiple molecular targets of caffeine and open the way for studying the relationship between caffeine and intracellular iron metabolism.
url http://europepmc.org/articles/PMC5033359?pdf=render
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