Related Experiment Video
Updated: Apr 17, 2026

05:51
A Human Ex Vivo Atherosclerotic Plaque Model to Study Lesion Biology
Published on: May 6, 2014
13.9K
Environmental carcinogens and mutational pathways in atherosclerosis.
A Pulliero1, R Godschalk2, M G Andreassi3
1Department of Health Sciences, University of Genoa, Italy.
International Journal of Hygiene and Environmental Health
|February 24, 2015
Summary
Environmental mutagens and DNA damage contribute to atherosclerosis development and progression. This review explores mutation-related pathways and oxidative stress in cardiovascular disease, highlighting molecular mechanisms.
Area of Science:
- Molecular Biology
- Cardiovascular Research
- Environmental Health
Background:
- Atherosclerosis is linked to DNA damage in blood and vessel cells.
- Environmental mutagens like polycyclic aromatic hydrocarbons and heavy metals are found in atherosclerotic vessels.
- Genetic variations in metabolic and DNA repair genes are associated with cardiovascular disease risk.
Purpose of the Study:
- To review experimental and clinical evidence on the role of mutation-related pathways in atherosclerosis.
- To examine the molecular mechanisms underlying DNA damage and oxidative stress in atherosclerosis.
- To explore the impact of environmental mutagens on cardiovascular disease pathogenesis.
Main Methods:
- Literature review of experimental animal models and human clinical studies.
- Analysis of molecular mechanisms involving DNA damage, oxidative stress, and apoptosis.
- Examination of the role of endogenous and exogenous mutagens in atherosclerosis.
Main Results:
- Chemical carcinogens and DNA adducts are abundant in atherosclerotic vessels.
- Mitochondrial DNA damage and oxidative stress contribute to plaque development and instability.
- Ionizing radiation is identified as a risk factor for atherosclerosis.
Conclusions:
- Mutation-related pathways and oxidative damage play a significant pathogenic role in atherosclerosis.
- Environmental and endogenous factors contribute to DNA damage, influencing cardiovascular disease prognosis.
- Further research is needed to clarify the role of UV radiation in atherosclerosis.
Related Concept Videos
Mutagenicity and Carcinogenicity
2.2K
Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...
2.2K
Atherosclerosis I: Introduction
2.2K
Atherosclerosis is a progressive disorder characterized by the buildup of plaques on the arterial inner wall, causing them to narrow and harden over time. These plaques comprise lipids, calcium, blood components, carbohydrates, and fibrous tissue. The process primarily affects the intima of large and medium-sized arteries, reducing blood flow in any artery.Etiology and risk factorsThe cause of atherosclerosis is multifactorial, involving a complex interplay among endothelial injury, lipid...
2.2K
Coronary Artery Disease I: Introduction
1.7K
Coronary Artery Disease (CAD): An Overview with Scientific InsightsCoronary Artery Disease (CAD), often referred to as C-A-D, is a prevalent blood vessel disorder classified under the broader category of atherosclerosis. Atherosclerosis is a pathological process characterized by the hardening and narrowing of arteries due to the accumulation of atherosclerotic plaques. These plaques are composed of cholesterol, fatty substances, inflammatory cells, calcium, and fibrin, reducing blood flow to...
1.7K
Mutations
98.4K
Overview
98.4K
Mutations
46.6K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
46.6K
Spontaneous and Induced Mutations
3.4K
Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).
3.4K

