Dietary ortho phenols that induce glutathione S-transferase and increase the resistance of cells to hydrogen peroxide are potential cancer chemopreventives that act by two mechanisms: the alleviation of oxidative stress and the detoxification of mutagenic xenobiotics
Abstract
Oxidative stress is implicated in the etiology of cancer, hence compounds that alleviate oxidative stress by inducing enzymes that defend against free radical damage might be useful as cancer chemopreventives. Glutathione S-transferase (GST) has been suggested to be a candidate for a critical enzyme in protecting cells against free radical damage, in part, because its level of induction correlates with protection of the cell line IMR-32 against hydrogen peroxide-induced oxidative stress. The present study identified dietary ortho phenols that both induce GST and protect the cell line IMR-32 against hydrogen peroxide-caused oxidative stress. The ortho phenol (o-phenol) inducers were better protectors against oxidative stress than a number of GST inducers that did not bear phenolic groups, possibly because the phenol residues of the ortho phenols allowed their action as antioxidants as well as inducers of GST. GST has previously been thought to protect cells against cancer by detoxifying mutagenic xenobiotics. The present results suggest that ortho phenol inducers of GST might be useful as cancer chemopreventives that act by two independent mechanisms, the alleviation of oxidative stress and the detoxification of mutagenic xenobiotics.
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Many GST protein family members act as tumor promoters by influencing reactive oxygen species (ROS).
“Many GST protein family members act as tumor promoters by influencing reactive oxygen species (ROS) (51–56).”
From The origin of hepatocellular carcinoma depends on metabolic zonation (2026) · cites this paper as [55]
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The origin of hepatocellular carcinoma depends on metabolic zonation
Guo, J., Liang, R., Chung, A., Li, Z., Li, B., Chen, E., Li, L., Wang, J., Hsieh, M.-H., Fang, I. X., et al. (2026) · Science · doi:10.1126/science.adv7129 · Cited by 24 · see citing works
- Authors
- Fiander, H.
- Affiliations
- Institute for Biological Sciences (CA)
- Corresponding author
- Fiander, H
- Venue
- Cancer Letters
- Publisher
- Elsevier BV
- Published
- 2000-08-11
- Volume
- 156
- Issue
- 2
- Pages
- 117-124
- ISSN
- 0304-3835 (ISSN-L)
- OpenAlex
- W1979300200
- Cited by
- 97
- References
- 0
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 2 · 2023: 6 · 2022: 1 · 2021: 4 · 2020: 4 · 2019: 2 · 2018: 3 · 2017: 4 · 2016: 4 · 2015: 4 · 2014: 5 · 2013: 4 · 2012: 4
- FWCI
- 1.57
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cancer Letters (publishedVersion)
- PubMed (publishedVersion)
- NPARC (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
- Health Sciences › Medicine › Biochemistry › Phytochemicals and Antioxidant Activities
- Keywords
- dietary phenolic compounds, glutathione S-transferase induction, chemoprevention, oxidative stress, hydrogen peroxide, antioxidant activity, IMR-32 cells, oxidative damage
- MeSH terms
- Antioxidants, Diet, Diterpenes, Enzyme Induction, Flavonoids, Glutathione Transferase, Humans, Hydrogen Peroxide, Isomerism, Inactivation, Metabolic, Mutagens, Phenanthrenes, Phenols, Plant Extracts, Structure-Activity Relationship, Tumor Cells, Cultured, Anticarcinogenic Agents, Oxidative Stress, Inhibitory Concentration 50, Flavonols, Abietanes
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