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Updated: Mar 16, 2026

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
Genetic and epigenetic cancer chemoprevention on molecular targets during multistage carcinogenesis
Hyung Sik Kim1, Sam Kacew2, Byung Mu Lee3
1Division of Toxicology, College of Pharmacy, Sungkyunkwan University, Seoburo 2066, Suwon, Gyeonggi-Do, 440-746, Republic of Korea.
Abstract:
The main goal of cancer chemoprevention is to prevent or halt the progression of carcinogenesis with the administration of synthetic or natural compounds. Fundamental chemopreventive strategies include inhibition of genetic damage, anti-proliferation/cell cycle regulation, and induction of apoptosis and anti-inflammatory processes, which may be critical for carcinogenesis intervention. Recently, a new paradigm for identifying chemopreventive agents has been implemented. It focuses on defining new biomarkers that can be used to evaluate chemopreventive efficacy based on multistage carcinogenesis. The functional roles of chemopreventive agents are associated with the modulation of nuclear factor kappa B, nuclear factor erythroid 2-related factor, p53, AMPK/mTOR, phosphatidylinositol 3-kinase, epidermal growth factor receptor, cyclooxygenase-2, chemokine (C-X-C motif) receptor 2, and sphingosine-1-phosphate. This paper summarizes the genetic and epigenetic effects of chemopreventive agents on the expression of cancer-related target genes mediated by epigenetic alterations, such as DNA methylation and histone modifications. This review will provide unique and effective strategies for reducing cancer and aging-related diseases in humans.
Insights
Cancer chemoprevention uses compounds to halt cancer progression by targeting genetic damage, cell cycles, and inflammation. New strategies identify biomarkers for efficacy, focusing on molecular pathways and epigenetic modifications for disease prevention.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Cancer chemoprevention aims to prevent or delay carcinogenesis using synthetic or natural compounds.
- Key strategies involve inhibiting genetic damage, regulating cell proliferation, inducing apoptosis, and reducing inflammation.
- A new paradigm focuses on biomarkers for evaluating chemopreventive efficacy across carcinogenesis stages.
Purpose of the Study:
- To summarize the genetic and epigenetic effects of chemopreventive agents on cancer-related genes.
- To highlight the role of epigenetic alterations like DNA methylation and histone modifications.
- To present strategies for reducing cancer and aging-related diseases.
Main Methods:
- Review of literature on cancer chemoprevention strategies.
- Analysis of molecular targets modulated by chemopreventive agents, including signaling pathways (NF-κB, Nrf2, p53, AMPK/mTOR, PI3K, EGFR, COX-2, CXCR2, S1P).
- Examination of genetic and epigenetic mechanisms (DNA methylation, histone modifications).
Main Results:
- Chemopreventive agents modulate key molecular pathways crucial for carcinogenesis intervention.
- Epigenetic alterations, including DNA methylation and histone modifications, play a significant role in mediating the effects of chemopreventive agents.
- Identification of specific biomarkers aids in evaluating the efficacy of chemopreventive agents.
Conclusions:
- Chemoprevention offers a promising approach to reduce cancer incidence and progression.
- Understanding the molecular and epigenetic mechanisms enhances the development of novel chemopreventive strategies.
- This review provides insights into effective strategies for combating cancer and aging-related diseases.
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