Abstract

Superoxide radicals, together with nitric oxide (NO), determine the oxidative status of cells, which use different pathways to control their levels in response to stressing conditions. Using gene expression data available in the Cancer Cell Line Encyclopedia and microarray results, we compared the expression of genes engaged in pathways controlling reactive oxygen species and NO production, neutralization, and changes in response to the exposure of cells to ionizing radiation (IR) in human cancer cell lines originating from different tissues. The expression of NADPH oxidases and NO synthases that participate in superoxide radical and NO production was low in all cell types. Superoxide dismutase, glutathione peroxidase, thioredoxin, and peroxiredoxins participating in radical neutralization showed high expression in nearly all cell types. Some enzymes that may indirectly influence superoxide radical and NO levels showed tissue-specific expression and differences in response to IR. Using fluorescence microscopy and specific dyes, we followed the levels and the distribution of superoxide and NO radicals in living melanoma cells at different times after exposure to IR. Directly after irradiation, we observed an increase of superoxide radicals and NO coexistent in the same subcellular locations, suggesting a switch of NO synthase to the production of superoxide radicals.

Highlights

  • Reactive oxygen species (ROS) appear in different metabolic reactions in organisms living in aerobic conditions

  • The activity of nitric oxide synthases (NOS) can be regulated by the nitric oxide synthase interacting protein (NOSIP) [46]

  • We show the results of analyses of the expression of genes coding for enzymes that participate in the regulation of cellular redox status, comparing the levels of transcripts for these genes in more than 1000 cell types from different tissues, including cancer cell lines

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Summary

Introduction

Reactive oxygen species (ROS) appear in different metabolic reactions in organisms living in aerobic conditions. The main representatives of ROS are superoxide radical (O2 − ), hydroxyl ( OH), singlet oxygen (1 O2 ), and hydrogen peroxide (H2 O2 ), which together with reactive nitrogen species such as nitric oxide (NO), peroxynitrite (ONOO− ), and nitrogen dioxide (NO2 ) are damaging agents causing death and involved in aging; they are important players in cellular regulation mechanisms and signaling pathways [1,2,3,4]. ROS may origin from endogenous or exogenous sources; endogenous sources include mitochondria, peroxisomes, and endoplasmic reticulum, where oxygen consumption is high [5]. Exogenous sources of ROS include ionizing and non-ionizing radiation, drugs, pollutants, food, ultrasound, xenobiotics, and toxins [6].

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