Literature DB >> 12810636

Persistent oxidative stress in chromosomally unstable cells.

Charles L Limoli1, Erich Giedzinski, William F Morgan, Steven G Swarts, George D D Jones, William Hyun.   

Abstract

Past work using the human-hamster hybrid line GM10115 has demonstrated that exposure to a variety of DNA damaging agents can lead to the persistent destabilization of chromosomes. To gain insight into the potential biochemical mechanisms involved in perpetuating the unstable phenotype, groups of clones characterized as stable or unstable were analyzed for indications of oxidative stress. All of the clones were derived from single progenitor cells surviving exposure to ionizing radiation or chemicals. Compared with their stable counterparts, unstable clones possessed elevated levels of reactive oxygen species (ROS) as measured by their enhanced ability to oxidize fluorogenic dyes. Fluorescence automated cell sorting analysis indicated that unstable clones had significantly higher mean fluorescence signals of approximately 2-fold and approximately 1.25-fold, respectively, as derived from the dyes 5-(and-6)-chloromethyl-2',7'-dichlorodihydrofluorescein diacetate and dihydrorhodamine 123, respectively. To determine whether mitochondria might constitute a potential source of ROS, stable and unstable clones of cells were analyzed for mitochondrial content using nonyl acridine orange and function using rhodamine 123. Fluorescence automated cell sorting data indicated that compared with stable clones, unstable clones possessed an elevated number (15% increase in mean nonyl acridine orange fluorescence) of dysfunctional mitochondria (27% decrease in mean rhodamine 123 fluorescence). Interestingly, the consequences of elevated ROS did not translate to an increase in oxidative base damage in nuclear DNA. Analysis of nine different base damage adducts by gas chromatography/mass spectrometry did not reveal significant differences between stable and unstable clones. The data suggest that the perpetuation of many of the abnormal phenotypes associated with genomic instability may be linked to a state of chronic oxidative stress derived in part from dysfunctional mitochondria.

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Keywords:  Non-programmatic

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Year:  2003        PMID: 12810636

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  54 in total

1.  Induction of chromosomal instability by chronic oxidative stress.

Authors:  Charles L Limoli; Erich Giedzinski
Journal:  Neoplasia       Date:  2003 Jul-Aug       Impact factor: 5.715

Review 2.  Reduction-oxidation (redox) system in radiation-induced normal tissue injury: molecular mechanisms and implications in radiation therapeutics.

Authors:  R Yahyapour; E Motevaseli; A Rezaeyan; H Abdollahi; B Farhood; M Cheki; S Rezapoor; D Shabeeb; A E Musa; M Najafi; V Villa
Journal:  Clin Transl Oncol       Date:  2018-01-09       Impact factor: 3.405

3.  Cytogenetic effects of low-dose radiation with different LET in human peripheral blood lymphocytes.

Authors:  E A Nasonova; N L Shmakova; O V Komova; L A Mel'nikova; T A Fadeeva; E A Krasavin; S Ritter
Journal:  Radiat Environ Biophys       Date:  2006-10-10       Impact factor: 1.925

Review 4.  Twilight effects of low doses of ionizing radiation on cellular systems: a bird's eye view on current concepts and research.

Authors:  Ilaria Postiglione; Angela Chiaviello; Giuseppe Palumbo
Journal:  Med Oncol       Date:  2009-06-06       Impact factor: 3.064

Review 5.  Health risks of space exploration: targeted and nontargeted oxidative injury by high-charge and high-energy particles.

Authors:  Min Li; Géraldine Gonon; Manuela Buonanno; Narongchai Autsavapromporn; Sonia M de Toledo; Debkumar Pain; Edouard I Azzam
Journal:  Antioxid Redox Signal       Date:  2013-12-06       Impact factor: 8.401

6.  Sensitivity to low-dose/low-LET ionizing radiation in mammalian cells harboring mutations in succinate dehydrogenase subunit C is governed by mitochondria-derived reactive oxygen species.

Authors:  Nukhet Aykin-Burns; Benjamin G Slane; Annie T Y Liu; Kjerstin M Owens; Malinda S O'Malley; Brian J Smith; Frederick E Domann; Douglas R Spitz
Journal:  Radiat Res       Date:  2010-11-17       Impact factor: 2.841

7.  Radiation-induced alterations in mitochondria of the rat heart.

Authors:  Vijayalakshmi Sridharan; Nukhet Aykin-Burns; Preeti Tripathi; Kimberly J Krager; Sunil K Sharma; Eduardo G Moros; Peter M Corry; Grazyna Nowak; Martin Hauer-Jensen; Marjan Boerma
Journal:  Radiat Res       Date:  2014-02-25       Impact factor: 2.841

Review 8.  Bystander effects and radiotherapy.

Authors:  Alicia Marín; Margarita Martín; Olga Liñán; Felipe Alvarenga; Mario López; Laura Fernández; David Büchser; Laura Cerezo
Journal:  Rep Pract Oncol Radiother       Date:  2014-08-28

9.  A role for mitochondrial dysfunction in perpetuating radiation-induced genomic instability.

Authors:  Grace J Kim; Gary M Fiskum; William F Morgan
Journal:  Cancer Res       Date:  2006-11-01       Impact factor: 12.701

10.  Mitochondrial dysfunction resulting from loss of cytochrome c impairs radiation-induced bystander effect.

Authors:  G Yang; L Wu; S Chen; L Zhu; P Huang; L Tong; Y Zhao; G Zhao; J Wang; T Mei; A Xu; Y Wang
Journal:  Br J Cancer       Date:  2009-05-19       Impact factor: 7.640

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