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Published on: October 23, 2017
Induced Cell Death as a Possible Pathway of Antimutagenic Action
N V Eremina1, A K Zhanataev1, A D Durnev2
1V. V. Zakusov Research Institute of Pharmacology, Russian Academy of Medical Sciences, Moscow, Russia.
Abstract:
The existing concepts of antimutagenesis are briefly reviewed. Published reports on antimutagenic and proapoptotic properties of some polyphenols and compounds of other chemical groups obtained in representative in vitro and in vivo experiments on eukaryotic test systems are discussed. The relationships between the antimutagenic and proapoptotic properties of the analyzed compounds (naringin, apigenin, resveratrol, curcumin, N-acetylcysteine, etc.) are considered in favor of the hypothesis on induced cell death as an antimutagenic tool.
Insights
Certain compounds, including polyphenols like resveratrol and curcumin, show antimutagenic and pro-apoptotic effects. This suggests that programmed cell death may serve as a mechanism for antimutagenesis.
Area of Science:
- Molecular Biology
- Genetics
- Pharmacology
Background:
- Antimutagenesis research explores compounds that prevent DNA mutations.
- Polyphenols and other natural compounds are investigated for their biological activities.
- Apoptosis, or programmed cell death, is a crucial cellular process.
Purpose of the Study:
- To review existing concepts of antimutagenesis.
- To discuss the antimutagenic and pro-apoptotic properties of various compounds.
- To explore the relationship between these two properties.
Main Methods:
- Literature review of published reports.
- Analysis of in vitro and in vivo experimental data.
- Focus on eukaryotic test systems.
Main Results:
- Several polyphenols (e.g., naringin, apigenin, resveratrol, curcumin) and N-acetylcysteine exhibit both antimutagenic and pro-apoptotic effects.
- Data from diverse eukaryotic test systems support these findings.
Conclusions:
- A strong correlation exists between the antimutagenic and pro-apoptotic activities of the studied compounds.
- Induced cell death is proposed as a significant mechanism underlying antimutagenesis.
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