Literature DB >> 15247030

Lysosomal redox-active iron is important for oxidative stress-induced DNA damage.

Tino Kurz1, Alan Leake, Thomas von Zglinicki, Ulf T Brunk.   

Abstract

Data show that specifically chelating lysosomal redox-active iron can prevent most H(2)O(2)-induced DNA damage. Lysosomes seem to contain the major pool of redox-active labile iron within the cell. Under oxidative stress conditions, this iron may then relocate to the nucleus and play an important role for DNA damage by taking part in Fenton reactions.

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Year:  2004        PMID: 15247030     DOI: 10.1196/annals.1297.048

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  4 in total

1.  Noxa couples lysosomal membrane permeabilization and apoptosis during oxidative stress.

Authors:  Colins O Eno; Guoping Zhao; Avinashnarayan Venkatanarayan; Bing Wang; Elsa R Flores; Chi Li
Journal:  Free Radic Biol Med       Date:  2013-06-14       Impact factor: 7.376

2.  Disruption of clathrin-mediated trafficking causes centrosome overduplication and senescence.

Authors:  Maciej B Olszewski; Panagiotis Chandris; Bum-Chan Park; Evan Eisenberg; Lois E Greene
Journal:  Traffic       Date:  2013-11-12       Impact factor: 6.215

3.  Crucial role of chelatable iron in silver nanoparticles induced DNA damage and cytotoxicity.

Authors:  Agnieszka Grzelak; Maria Wojewódzka; Sylwia Meczynska-Wielgosz; Mariusz Zuberek; Dominika Wojciechowska; Marcin Kruszewski
Journal:  Redox Biol       Date:  2018-01-09       Impact factor: 11.799

Review 4.  Cell Death Pathways: a Novel Therapeutic Approach for Neuroscientists.

Authors:  G Morris; A J Walker; M Berk; M Maes; B K Puri
Journal:  Mol Neurobiol       Date:  2017-10-19       Impact factor: 5.590

  4 in total

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