Cell Proliferation, Reactive Oxygen and Cellular Glutathione
Open accessAbstract
A variety of cellular activities, including metabolism, growth, and death, are regulated and modulated by the redox status of the environment. A biphasic effect has been demonstrated on cellular proliferation with reactive oxygen species (ROS)—especially hydrogen peroxide and superoxide—in which low levels (usually submicromolar concentrations) induce growth but higher concentrations (usually >10–30 micromolar) induce apoptosis or necrosis. This phenomenon has been demonstrated for primary, immortalized and transformed cell types. However, the mechanism of the proliferative response to low levels of ROS is not well understood. Much of the work examining the signal transduction by ROS, including H 2 O 2 , has been performed using doses in the lethal range. Although use of higher ROS doses have allowed the identification of important signal transduction pathways, these pathways may be activated by cells only in association with ROS-induced apoptosis and necrosis, and may not utilize the same pathways activated by lower doses of ROS associated with increased cell growth. Recent data has shown that low levels of exogenous H 2 O 2 up-regulate intracellular glutathione and activate the DNA binding activity toward antioxidant response element. The modulation of the cellular redox environment, through the regulation of cellular glutathione levels, may be a part of the hormetic effect shown by ROS on cell growth.
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- Authors
- Day, R. M., & Suzuki, Y. J.
- Affiliations
- Uniformed Services University of the Health Sciences (US)
- Georgetown University (US)
- Corresponding author
- Day, Regina M.
- Venue
- Dose-Response
- Publisher
- SAGE Publications
- Published
- 2005-07-01
- Volume
- 3
- Issue
- 3
- Pages
- 425-42
- ISSN
- 1559-3258 (ISSN-L)
- PMC
- PMC2475947
- OpenAlex
- W1968883706
- Cited by
- 149
- References
- 88
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 9 · 2023: 9 · 2022: 9 · 2021: 16 · 2020: 23 · 2019: 10 · 2018: 11 · 2017: 5 · 2016: 10 · 2015: 8 · 2014: 4 · 2013: 3 · 2012: 8
- FWCI
- 0.13
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Dose-Response (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ScholarWorks@UMassAmherst (University of Massachusetts Amherst) (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Australian Government
- National Institutes of Health (5r01hl073929-05)
- Uniformed Services University of the Health Sciences
- National Heart, Lung, and Blood Institute (R01-HL-073929, R01HL067340, R01HL072844)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer and biochemical research
- Keywords
- reactive oxygen species, hydrogen peroxide, superoxide, glutathione, cell proliferation, redox state, hormesis, antioxidant response element, DNA binding, apoptosis, necrosis, signal transduction
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