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Genotoxicity

Genotoxicity is the property of certain chemical, physical, or biological agents to induce damage to the genetic material within cells, primarily through alterations to DNA structure or function, such as mutations, chromosomal breaks, or recombination events.^[1] This damage can manifest as direct interactions with DNA—via mechanisms like alkylation, intercalation, or adduct formation—or indirectly through the generation of reactive oxygen species that cause oxidative stress and strand breaks.^[2] Genotoxins are distinguished from other toxicants by their potential to cause heritable changes in germ cells or oncogenic transformations in somatic cells, making genotoxicity a key concern in toxicology and risk assessment.^[3] The assessment of genotoxicity plays a pivotal role in regulatory frameworks for evaluating the safety of pharmaceuticals, environmental chemicals, food additives, and consumer products, as it helps identify substances that may pose carcinogenic or mutagenic risks to humans.^[4] Standard genotoxicity testing batteries, recommended by organizations like the International Council for Harmonisation (ICH), typically include a combination of in vitro assays—such as the bacterial reverse mutation (Ames) test for point mutations and the chromosomal aberration test in mammalian cells—and in vivo methods like the micronucleus assay to detect clastogenic effects.^[5] These tests aim to detect both DNA-reactive genotoxins, which operate without a threshold dose, and non-DNA-reactive ones that may act through epigenetic or physiological mechanisms, thereby informing hazard identification and exposure limits.^[6] Beyond immediate DNA damage, genotoxicity contributes to broader health outcomes, including carcinogenesis, reproductive toxicity, and developmental disorders, underscoring its significance in molecular epidemiology and personalized medicine. Advances in genotoxicity evaluation, such as high-throughput in silico models including AI-driven predictions and New Approach Methodologies (NAMs), and biomarker-based approaches like the comet assay for DNA strand breaks, are enhancing predictive accuracy and reducing reliance on animal testing, while addressing challenges like false positives from non-relevant endpoints.^[7]^[8] Ongoing research emphasizes integrating genotoxicity data with toxicogenomics to better understand mode-of-action and threshold concepts for non-genotoxic carcinogens.^[2]

Definition and Fundamentals

Core Definition

Genotoxicity refers to the property of chemical, physical, or biological agents that damage the genetic material within a cell, particularly DNA, potentially leading to mutations, chromosomal aberrations, or cell death.^[3] This damage disrupts the integrity of the genome, which is essential for maintaining cellular function and organismal health. To contextualize genotoxicity, it is helpful to recall the basic structure and replication of DNA: DNA consists of two antiparallel strands forming a double helix, composed of nucleotide bases (adenine, thymine, guanine, and cytosine) linked by phosphodiester bonds, and replication occurs semiconservatively during the cell cycle, where each parental strand serves as a template for synthesizing a complementary daughter strand using DNA polymerase enzymes.^[9]^[10] Genotoxic agents can exert their effects through direct interactions with DNA, such as alkylation or intercalation that covalently modify or insert into the DNA structure, or through indirect mechanisms, including the generation of reactive oxygen species that cause oxidative stress and subsequent DNA lesions like base modifications or strand breaks.^[11]^[12] These processes interfere with DNA replication and repair, increasing the likelihood of heritable genetic changes if the damage persists.^[13] In contrast to non-genotoxic carcinogens, which promote tumor development through mechanisms like hormonal disruption or chronic inflammation without directly altering DNA, genotoxic agents are distinguished by their potential to induce primary genomic instability.^[14] The assessment of genotoxic risk involves ongoing debate regarding threshold models versus no-threshold assumptions: while non-genotoxic effects are generally considered to have a safe exposure threshold below which no adverse effects occur, genotoxic carcinogens are often regulated under a no-threshold model due to the linear extrapolation of risk from low doses, though evidence for practical thresholds in DNA repair capacity continues to be explored.^[6]^[15]^[16]

Historical Context

The concept of genotoxicity traces its roots to pivotal advancements in molecular biology during the mid-20th century. In 1944, Oswald Avery, Colin MacLeod, and Maclyn McCarty provided experimental evidence that deoxyribonucleic acid (DNA) serves as the genetic material, demonstrating its ability to transform non-virulent bacteria into virulent strains through purified extracts. This discovery shifted scientific focus from proteins to nucleic acids as carriers of hereditary information. Complementing this, James Watson and Francis Crick proposed the double-helix structure of DNA in 1953, elucidating how genetic information could be stored, replicated, and potentially damaged, laying the groundwork for understanding mutagenic effects.^[17] Post-World War II, heightened awareness of environmental hazards, including radiation from atomic testing and industrial chemicals, fueled research into chemical mutagens during the 1960s. A landmark event was the identification of aflatoxin B1 in 1960 as a potent hepatocarcinogen produced by Aspergillus fungi, linking mold-contaminated feed to widespread livestock poisoning and highlighting the risks of naturally occurring genotoxic agents.^[18] The term "genotoxicity" was coined in the 1970s— with its earliest documented use in 1978 in the journal Mutation Research—to describe the capacity of agents to induce genetic damage, amid escalating concerns over synthetic chemicals in the environment.^[19] This era was transformed by Bruce Ames's development of the Ames test in 1975, a bacterial reverse mutation assay that rapidly screened compounds for mutagenic potential, influencing global safety assessments.^[4] By the 1980s, genotoxicity had solidified in regulatory science, with organizations like the Organisation for Economic Co-operation and Development (OECD) adopting standardized tests, such as Test Guideline 474 for the in vivo micronucleus assay in 1983, to evaluate chromosomal damage in rodents. The 1990s expanded the field beyond classical mutagenesis, incorporating assays like the single-cell gel electrophoresis (comet) assay, first described in 1984 but widely adopted in the 1990s for visualizing DNA strand breaks at the individual cell level. Regulatory harmonization advanced through the International Council for Harmonisation (ICH), which issued Guideline S2A in 1995 and S2B in 1997, establishing a core battery of genotoxicity tests for pharmaceuticals, including gene mutation, chromosomal aberration, and in vivo assays.^[20]^[21]^[22] Entering the 2020s, while the core definition of genotoxicity remains focused on DNA damage, research has increasingly explored related fields like epigenotoxicity, involving mechanisms such as histone modifications and RNA alterations that induce heritable changes without direct DNA sequence disruption. This evolution reflects growing recognition of gene-environment interactions in disease, prompting calls for integrated testing of genotoxicity and epigenotoxicity in regulatory frameworks to address dynamic, context-dependent effects, including advanced assays like dual-directional epi-genotoxicity methods as of 2025.^[23]^[4]^[24]

Mechanisms of Action

Types of DNA Damage

Genotoxicity involves various forms of damage to the genetic material, primarily targeting DNA at the molecular level. These damages can be broadly classified into base modifications, strand breaks, crosslinks, and chromosomal aberrations, each arising from distinct chemical or physical interactions that disrupt DNA structure and function.^[25] Base modifications encompass alterations to individual nucleotide bases, such as alkylation, deamination, and oxidation. Alkylation adds alkyl groups to bases like guanine, forming lesions such as O⁶-methylguanine, which can lead to base mispairing during replication. Deamination converts bases like cytosine to uracil through spontaneous hydrolysis, creating mismatched pairs that promote transitions. Oxidation, often from reactive oxygen species, generates oxidized bases like 8-oxoguanine, which pairs erroneously with adenine instead of cytosine. These modifications are typically small-scale and repaired by base excision repair (BER), which recognizes and excises the damaged base, replacing it with the correct nucleotide via DNA polymerase and ligase. UV radiation forms pyrimidine dimers, such as cyclobutane pyrimidine dimers (CPDs), which distort the helix and are primarily excised by nucleotide excision repair (NER); if unrepaired, CPDs account for the majority of UV-induced mutations.^[25]^[26]^[27] Strand breaks include single-strand breaks (SSBs) and double-strand breaks (DSBs), which sever the phosphodiester backbone. SSBs occur frequently from oxidative stress or enzymatic activity, with an estimated 10,000 SSBs generated per mammalian cell per day, primarily repaired by BER through end-processing and ligation.^[28] DSBs, more severe, result from ionizing radiation that produces reactive hydroxyl radicals, cleaving both strands and posing a high risk of genomic rearrangement if unrepaired; non-homologous end joining (NHEJ) ligates the broken ends, often introducing small insertions or deletions.^[25]^[26] Crosslinks involve covalent bonds between DNA strands or within a strand, impeding replication and transcription. Interstrand crosslinks (ICLs) link opposite strands, commonly induced by bifunctional alkylating agents, and require coordinated repair involving nucleotide excision repair (NER) to excise the lesion followed by homologous recombination or NHEJ for strand restoration. Intrastrand crosslinks, such as those between adjacent purines, distort the helix and are also primarily addressed by NER.^[25] Chromosomal aberrations represent larger-scale structural changes, including deletions and translocations, often stemming from unrepaired DSBs or replication errors. Deletions remove segments of DNA, while translocations exchange material between chromosomes, both contributing to genomic instability; these are mitigated by NHEJ or homologous recombination, though failures amplify the damage. A classic mechanism for initiating such aberrations is ionizing radiation, which triggers DSBs via clustered damage sites.^[25]^[26] Overall, cells encounter thousands of DNA lesions daily, including approximately 10,000 abasic sites and oxidative lesions per cell, alongside the spontaneous mutation rate of about 10^{-9} per base pair per replication, underscoring the constant challenge to genomic fidelity. Failure in repair pathways like BER for small lesions, NER for bulky adducts, and NHEJ for breaks can propagate these damages into permanent mutations. Direct and indirect genotoxins initiate these damage types through reactive intermediates or physical disruption.^[25]^[29]

Direct and Indirect Genotoxins

Genotoxins are classified into direct and indirect categories based on their mechanism of interaction with DNA. Direct genotoxins are chemically reactive compounds that can bind covalently to DNA without requiring metabolic activation, leading to the formation of DNA adducts that disrupt replication and transcription.^[30] In contrast, indirect genotoxins are relatively inert in their parent form and must undergo bioactivation, typically by cellular enzymes, to generate reactive intermediates capable of damaging DNA.^[31] These interactions ultimately result in various types of DNA lesions, such as base modifications or strand breaks.^[32] Direct genotoxins, such as alkylating agents, exert their effects rapidly by forming stable covalent bonds with nucleophilic sites on DNA bases, particularly guanine residues. A classic example is sulfur mustard (mustard gas), which alkylates the N7 position of guanine and other sites, creating cross-links and monoadducts that impede DNA processing and trigger repair pathways.^[33] Unlike indirect agents, direct genotoxins do not rely on enzymatic conversion, allowing them to induce damage in any cellular environment, though their reactivity can also lead to non-specific binding to other biomolecules.^[34] Indirect genotoxins require metabolic bioactivation to become genotoxic, often involving cytochrome P450 enzymes that convert them into electrophilic species. For instance, benzene is oxidized by cytochrome P450 2E1 to benzene oxide and other epoxides, which can form DNA adducts or decompose to generate reactive oxygen species (ROS) that cause oxidative base damage, such as 8-oxoguanine.^[31] Similarly, these agents can indirectly promote genotoxicity through ROS-mediated oxidation of DNA, leading to single-strand breaks and mutations if unrepaired.^[35] Certain indirect genotoxins, known as pro-genotoxins, are activated to ultimate genotoxins that form mixtures of reactive metabolites. Polycyclic aromatic hydrocarbons (PAHs), such as benzopyrene, exemplify this class; they are metabolized by cytochrome P450 enzymes to diol-epoxides that covalently bind to DNA, forming bulky adducts primarily at the N2 position of guanine.^[36] These pro-genotoxins highlight the role of phase I metabolism in converting stable compounds into highly reactive forms capable of persistent DNA damage.^[37] Detecting direct versus indirect genotoxins presents distinct challenges due to differences in their activation requirements. Direct genotoxins produce rapid, observable effects in simple test systems, as their reactivity does not depend on external factors.^[38] However, indirect genotoxins often yield false negatives in assays lacking metabolic competence, such as standard bacterial mutagenicity tests without exogenous enzyme fractions, because their bioactivation relies on mammalian-like metabolic pathways like cytochrome P450 activity.^[39] This dependency necessitates specialized systems, such as those incorporating S9 liver fractions, to mimic in vivo conditions and ensure accurate identification.^[40]

Detection and Assessment Methods

In Vitro Testing Techniques

In vitro genotoxicity testing techniques employ mammalian cell cultures to evaluate the potential of chemicals to induce genetic damage, such as mutations, chromosomal aberrations, or DNA strand breaks, in a controlled laboratory setting outside living organisms. These methods typically use established cell lines like Chinese hamster ovary (CHO) cells, V79 Chinese hamster lung fibroblasts, or primary human lymphocytes, which are exposed to test substances under standardized conditions to measure specific endpoints of genotoxicity.^[41]^[42]^[43] Key assays include the in vitro mammalian cell micronucleus test, which detects clastogenic (chromosome-breaking) and aneugenic (chromosome-losing) effects by identifying micronuclei—small extranuclear bodies containing chromosome fragments or whole chromosomes—in interphase cells, as outlined in OECD Test Guideline 487 (updated June 2025).^[44] The hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene mutation assay, described in OECD Test Guideline 476 (updated June 2025), quantifies forward mutations at the HPRT locus on the X chromosome, where mutant cells survive in selective media containing 6-thioguanine, indicating base-pair substitutions, frameshifts, or small deletions.^[41] Additionally, the sister chromatid exchange (SCE) assay, previously standardized in OECD Test Guideline 479 before its delisting in 2014, visualizes reciprocal DNA exchanges between sister chromatids using differential staining with bromodeoxyuridine incorporation, serving as a sensitive indicator of DNA damage repair and recombination events.^[45]^[46] These techniques offer advantages such as highly controlled experimental conditions that allow precise dosing and endpoint analysis, enabling high-throughput screening of multiple compounds.^[47] The incorporation of an exogenous metabolic activation system, typically Aroclor 1254- or phenobarbital/β-naphthoflavone-induced rat liver S9 fraction mixed with cofactors like NADPH, simulates phase I and II hepatic metabolism to detect promutagens requiring bioactivation.^[48]^[49] However, in vitro methods have limitations, including the absence of complex physiological interactions, such as tissue-specific metabolism, immune responses, or DNA repair pathways present in whole organisms, which can lead to discrepancies with in vivo outcomes.^[50] High cytotoxicity from test substances, often exceeding 50% cell death or growth inhibition, can produce false-positive genotoxicity results by inducing secondary DNA damage through apoptosis or necrosis, necessitating careful cytotoxicity assessments to validate findings.^[51]^[52]

In Vivo Testing Techniques

In vivo testing techniques for genotoxicity involve the administration of test substances to whole living organisms, primarily rodents such as mice and rats, to evaluate DNA damage and mutagenic potential under physiological conditions. These methods commonly employ transgenic rodent models, like the Big Blue mouse, which carry integrated reporter genes for mutation detection, or standard rodents for cytogenetic endpoints. Endpoints assessed include DNA adducts—covalent modifications of DNA by genotoxic agents—in various tissues, providing insights into systemic exposure and repair processes. Human biomonitoring studies complement animal data by measuring DNA adducts in accessible tissues like blood or urine from exposed populations, offering direct evidence of genotoxic risk in real-world scenarios.^[53] Key in vivo assays include the unscheduled DNA synthesis (UDS) test in mammalian liver cells, which detects DNA repair activity following exposure by quantifying nucleotide incorporation outside of S-phase replication. In this assay, rodents are treated with the test substance, and hepatocytes are isolated to measure silver grain counts over nuclei as an indicator of repair synthesis, as standardized in OECD Test Guideline 486 (updated June 2025). Transgenic rodent mutation assays, such as the Big Blue system, utilize mice or rats harboring the lacI transgene; mutations are recovered from tissues like bone marrow or liver by packaging DNA into bacteriophage and plating on indicator bacteria, allowing quantification of point mutations and small deletions, as per OECD Test Guideline 488 (updated June 2025). The bone marrow micronucleus assay evaluates clastogenic and aneugenic effects by scoring micronuclei in polychromatic erythrocytes post-exposure, typically 24-48 hours after treatment, per OECD Test Guideline 474 (updated June 2025), which requires analysis of at least 4,000 cells per animal to detect chromosomal aberrations.^[54]^[55]^[56]^[57] These techniques offer significant advantages over in vitro methods by incorporating absorption, distribution, metabolism, and excretion (ADME) processes, which influence the delivery of active metabolites to target sites. They enable detection of organ-specific genotoxic effects, such as liver-specific damage in UDS assays, reflecting the complexity of whole-body pharmacokinetics and DNA repair mechanisms absent in cell-based systems. In vivo assays thus provide higher relevance for risk assessment, confirming or refuting in vitro positives through physiological context.^[49]^[58] Ethical and practical considerations in in vivo genotoxicity testing emphasize the 3Rs principle—replacement, reduction, and refinement of animal use—as integrated into OECD guidelines to minimize welfare impacts. For instance, transgenic assays like OECD 488 reduce animal numbers by enabling mutation analysis in multiple tissues from fewer individuals, while refinements such as humane endpoints and optimized dosing schedules limit suffering. Compliance with these guidelines ensures reproducibility and ethical conduct, balancing scientific needs with animal welfare.^[59]^[60]

Specialized Assays

The Ames test, also known as the bacterial reverse mutation assay, employs histidine-requiring strains of Salmonella typhimurium (such as TA98, TA100, TA1535, and TA1537) and tryptophan-requiring strains of Escherichia coli (such as WP2 uvrA) to detect point mutations that restore the ability to synthesize these amino acids, allowing revertant colonies to grow on minimal media.^[48]^[61] The assay incorporates metabolic activation using a rat liver S9 fraction (5-30% v/v) to simulate mammalian metabolism, enabling detection of promutagens that require bioactivation.^[48] It identifies base-pair substitutions and frameshift mutations. The Comet assay, or single cell gel electrophoresis, quantifies DNA strand breaks in individual cells by embedding them in agarose, lysing to release nucleoids, and applying an electric field under alkaline or neutral conditions, where damaged DNA migrates to form a "tail" visualized by fluorescence microscopy.^[62] The tail moment, calculated as the product of tail length and the fraction of DNA in the tail, serves as a primary measure of damage extent, offering quantitative assessment applicable to diverse cell types including those from human, animal, and plant sources.^[63] The alkaline version detects single-strand breaks and alkali-labile sites, while the neutral version primarily identifies double-strand breaks, allowing tailored evaluation of specific lesion types.^[62]^[64] The Pig-a assay assesses in vivo gene mutations by measuring deficiencies in glycosylphosphatidylinositol (GPI) anchors on erythrocyte surfaces, resulting from inactivating mutations in the X-linked Pig-a gene, using flow cytometry to enumerate mutant reticulocytes and erythrocytes in peripheral blood samples, as described in OECD Test Guideline 470 (adopted 2022, updated June 2025).^[65] This method integrates physiological processes like absorption and DNA repair in rodent models, typically over a 28-day repeat-dose protocol, providing a sensitive indicator of mutagenic potential with high concordance to other genotoxicity endpoints.^[65]^[66] Flow cytometry-based methods enable high-throughput genotoxicity screening by rapidly analyzing thousands of cells for markers like micronuclei, which indicate chromosomal damage, using nucleic acid dyes to differentiate micronuclei from intact nuclei in cell populations.^[67] For instance, the flow cytometry micronucleus assay processes up to 20,000 cells per sample, surpassing traditional microscopy-based approaches in speed and sensitivity, and has been validated for nanomaterials and other agents in cell lines like BEAS-2B.^[67] Imaging flow cytometry further enhances this by combining high-resolution imaging with quantitative flow analysis for automated micronucleus detection in unlysed cells.^[68] These specialized assays form part of harmonized regulatory frameworks, such as the ICH S2(R1) guideline, which mandates the Ames test in the standard genotoxicity battery and endorses the Comet assay as an in vivo option for detecting DNA strand breaks, often in combination with micronucleus testing for comprehensive screening.^[49]

Health and Biological Impacts

Association with Cancer

Genotoxicity plays a central role in carcinogenesis by damaging DNA and inducing mutations that disrupt normal cellular control mechanisms. In the multistage model of cancer development, genotoxins primarily act as initiators during the initial phase, where they cause irreversible genetic alterations in key regulatory genes. These include activating mutations in oncogenes such as RAS, which promote uncontrolled cell proliferation, and inactivating mutations in tumor suppressor genes like TP53, which impair DNA repair and apoptosis pathways. Subsequent stages of promotion and progression involve additional genetic or epigenetic hits, often from repeated exposures or endogenous processes, leading to malignant transformation.^[69]^[70]^[71] Strong evidence for the genotoxic basis of carcinogenesis comes from classifications by the International Agency for Research on Cancer (IARC), which designates many Group 1 carcinogens—known to cause cancer in humans—as genotoxic agents. For instance, asbestos fibers induce DNA strand breaks, chromosomal aberrations, and oxidative damage, contributing to lung cancer and mesothelioma through direct genotoxic effects. Similarly, epidemiological studies have established a clear link between aflatoxin B1 exposure, a genotoxic mycotoxin produced by Aspergillus fungi, and hepatocellular carcinoma, particularly in regions with high contamination of staple foods like maize and peanuts; this association is synergistic with hepatitis B virus infection and supported by cohort studies showing dose-dependent risk increases.^[72]^[73]^[74]^[75] Genotoxins contribute substantially to the global burden of cancer, with environmental and lifestyle-related exposures implicated in a significant proportion (estimated at 90-95% in some studies) of cases, many through mutagenic DNA damage.^[76] Among the most common cancers—lung, breast, colorectal, and prostate—genotoxic agents play prominent roles; for example, benzopyrene in tobacco smoke forms DNA adducts that lead to TP53 mutations and G-to-T transversions characteristic of lung tumors in smokers, accounting for a significant portion of the 1.8 million annual lung cancer deaths worldwide.^[77]^[76]^[78] In therapeutic contexts, genotoxic chemotherapeutic agents like cisplatin exploit DNA damage to target rapidly dividing cancer cells by forming intrastrand crosslinks that inhibit replication and transcription. However, this mechanism carries a risk of secondary malignancies, particularly therapy-related leukemias, due to persistent mutagenicity in hematopoietic stem cells; studies in ovarian and testicular cancer survivors show a 2- to 40-fold elevated risk of acute myeloid leukemia within 5-10 years post-treatment, attributed to cisplatin's genotoxic footprint.^[79]^[80]

Links to Other Diseases

Genotoxicity contributes to various non-cancerous conditions by inducing mutations that disrupt normal cellular and organismal function. In genetic disorders, defects in DNA repair pathways exacerbate the effects of genotoxic agents, leading to hereditary diseases. For instance, xeroderma pigmentosum (XP) arises from mutations in nucleotide excision repair (NER) genes, impairing the removal of UV-induced DNA lesions such as cyclobutane pyrimidine dimers (CPDs) and 6-4 photoproducts (6-4PPs), which results in extreme photosensitivity, premature skin aging, and neurological degeneration in some patients.^[81] This amplification of UV genotoxicity highlights how inherited repair deficiencies convert environmental exposures into persistent genomic instability.^[81] Organ-specific toxicities further illustrate genotoxicity's broader impacts. In the kidneys, genotoxic nephrotoxins like cisplatin form DNA adducts, particularly intrastrand crosslinks between guanine residues in proximal tubular epithelial cells, triggering p53-mediated apoptosis and acute kidney injury (AKI) in up to 30-40% of treated patients.^[82] Similarly, in the brain, reactive oxygen species (ROS)-induced genotoxic stress contributes to neurotoxicity observed in Parkinson's disease models, where oxidative DNA damage, such as 8-oxoguanine lesions, accumulates in dopaminergic neurons of the substantia nigra, promoting neuronal death and inflammation.^[83] These mechanisms overlap with cancer pathways, such as TP53 activation in response to DNA damage, but manifest as tissue-specific degeneration rather than uncontrolled proliferation.^[84] Reproductive toxicity from genotoxins targets germ cells, increasing heritable risks through chromosomal instability. Folate deficiency, a common nutritional shortfall, disrupts DNA synthesis and repair, leading to uracil misincorporation and enhanced chromosomal nondisjunction, particularly at fragile sites rich in CG repeats on chromosomes like 2, which can result in aneuploidy and infertility.^[85] This genotoxic effect elevates the incidence of heritable disorders by impairing meiotic segregation.^[85] Accumulated DNA damage in somatic cells drives aging and chronic diseases by promoting genomic instability over time. In neurodegeneration, unrepaired oxidative lesions in post-mitotic neurons, coupled with declining base excision repair (BER), contribute to conditions like Parkinson's and Alzheimer's through mitochondrial dysfunction and ROS amplification.^[86] For cardiovascular issues, somatic DNA damage in vascular cells, including mitochondrial DNA deletions, fosters endothelial dysfunction, atherosclerosis, and fibrosis via chronic inflammation and impaired repair.^[86] These processes underscore genotoxicity's role in progressive, age-related decline across multiple systems.^[86]

Sources and Examples of Genotoxins

Environmental and Occupational Exposures

Environmental exposures to genotoxins occur primarily through air and water pollutants, which can enter the body via inhalation, ingestion, or dermal contact. Polycyclic aromatic hydrocarbons (PAHs), formed during incomplete combustion of organic materials such as fossil fuels, wood, and tobacco, are widespread airborne contaminants that exhibit genotoxic effects by forming DNA adducts, leading to mutations and increased cancer risk in exposed populations.^[87] Heavy metals like cadmium, often present in tobacco smoke and industrial emissions, contribute to genotoxicity through oxidative stress and DNA damage; tobacco contains cadmium at levels of 1-2 μg per cigarette, of which smokers inhale approximately 0.1-0.5 μg via mainstream smoke, elevating risks for lung and other cancers.^[88] Radon, a naturally occurring radioactive gas from uranium decay in soil and rock, seeps into buildings and is the leading cause of lung cancer among non-smokers, with genotoxic alpha particles from its decay products damaging lung cell DNA upon inhalation.^[89] Occupational exposures pose significant genotoxic risks in industries involving chemical handling. Benzene, a volatile organic compound used in petrochemical production, rubber manufacturing, and fuel refining, is metabolized to reactive intermediates that form DNA adducts, strongly associating with acute myeloid leukemia; workers exposed to levels above 1 ppm over years face up to a 5-fold increased risk.^[90] Pesticides, such as glyphosate in herbicides, have debated genotoxic potential based on 2020s reviews, with some studies indicating DNA damage in exposed agricultural workers via oxidative stress, while regulatory assessments like the EPA's conclude low risk at typical exposure levels below the chronic population-adjusted dose (cPAD) of 1.0 mg/kg body weight per day.^[91]^[92] Dietary genotoxins arise from contaminated foods, contributing to chronic low-level exposures. Mycotoxins like aflatoxin B1, produced by Aspergillus fungi on nuts, grains, and spices in warm, humid climates, are highly genotoxic, binding to DNA and causing liver mutations; the WHO estimates that approximately 4.5 billion people in developing regions are at risk, with average exposures of 1-10 ng/kg body weight daily leading to 25,000-155,000 hepatocellular carcinoma cases annually.^[93] Acrylamide, formed in starchy foods like fried potatoes and baked goods through the Maillard reaction at temperatures above 120°C, induces genotoxicity via glycidamide metabolites that alkylate DNA; global dietary exposure averages 0.4-1.9 μg/kg body weight daily, with fried products accounting for up to 50% of intake in high-consumption populations.^[94]^[95] Global trends amplify genotoxin exposures, particularly through urbanization and emerging contaminants. Rapid urban growth increases proximity to traffic-related PAHs and heavy metals, elevating inhalation risks in densely populated areas compared to rural settings.^[96] Studies from the 2020s highlight microplastics as potential carriers of genotoxins, adsorbing PAHs, heavy metals, and pesticides in aquatic and atmospheric environments before entering food chains; human exposures via seafood and drinking water may reach 10^4-10^5 particles annually, potentially exacerbating genotoxic effects through combined oxidative stress and bioaccumulation.^[97]^[98] Per- and polyfluoroalkyl substances (PFAS), persistent environmental contaminants in water and consumer products, induce genotoxicity through reactive oxygen species and DNA adducts, with ongoing 2025 regulatory scrutiny by the EPA.^[99]

Therapeutic and Industrial Agents

Therapeutic agents, particularly chemotherapeutic drugs, are intentionally genotoxic to target rapidly dividing cancer cells, but their use requires careful management due to off-target DNA damage in healthy tissues.^[100] Alkylating agents, such as cyclophosphamide, exert their effects by forming interstrand crosslinks between DNA bases like guanine, which block replication and transcription, leading to cell death or mutations.^[100] Antimetabolites like 5-fluorouracil incorporate into DNA during synthesis, causing chain termination and depleting nucleotide pools, which triggers futile repair cycles and double-strand breaks.^[100] Topoisomerase inhibitors, including etoposide, stabilize enzyme-DNA cleavage complexes, resulting in persistent double-strand breaks that overwhelm cellular repair mechanisms.^[100] In industrial settings, certain chemicals serve as genotoxins either as primary reactants or byproducts in manufacturing processes. Vinyl chloride, a key monomer in polyvinyl chloride (PVC) plastic production, is metabolically activated by cytochrome P450 enzymes to chloroethylene oxide, an epoxide that alkylates DNA bases to form etheno adducts, such as 1,N²-ethenodeoxyguanosine, promoting mutations.^[101] Azo dyes, widely used in textile and leather industries, undergo reductive cleavage by azoreductases in mammalian and microbial systems, yielding aromatic amines that can form DNA-reactive nitrenium ions, leading to adduct formation and genotoxic effects.^[102] Plastics additives like bisphenol A (BPA), employed in polycarbonate and epoxy resins, induce DNA strand breaks and micronuclei formation through oxidative stress and direct alkylation, as observed in cellular assays.^[103] The risk-benefit profile of these agents underscores their therapeutic value against the potential for secondary malignancies; for instance, alkylating agent-based chemotherapy elevates leukemia risk by approximately 5-fold, with absolute incidences around 1-2% in breast cancer survivors over 10 years.^[104] Etoposide contributes to therapy-related acute myeloid leukemia in 1-5% of cases, particularly at cumulative doses exceeding 2 g/m².^[105] To mitigate such risks, targeted biologics like monoclonal antibodies (e.g., trastuzumab) and checkpoint inhibitors (e.g., nivolumab) have emerged in the 2020s, selectively modulating signaling pathways or immune responses without inducing broad DNA damage, thereby lowering secondary cancer potential compared to traditional cytotoxics.^[106] These agents briefly link to increased cancer incidence via genotoxic mechanisms but are increasingly supplemented by precision approaches to balance efficacy and safety.

Risk Management and Regulation

Testing Standards and Guidelines

The International Council for Harmonisation (ICH) S2(R1) guideline establishes the standard battery for genotoxicity testing of pharmaceuticals intended for human use, recommending a core set of assays including the bacterial reverse mutation test (Ames test), an in vitro mammalian cell gene mutation test, and an in vivo test for chromosomal damage such as the micronucleus assay, with options to integrate transgenic rodent assays or the in vivo comet assay as follow-ups.^[5] This framework adopts a tiered approach, starting with in vitro screening to identify potential genotoxins, followed by confirmatory in vivo studies if initial results are positive, and emphasizes a weight-of-evidence evaluation to resolve equivocal findings by considering factors like exposure levels and mechanistic data.^[107] For equivocal results, additional assays or expert judgment are advised to avoid unnecessary animal testing while ensuring human risk prediction. In the European Union, the REACH regulation (Registration, Evaluation, Authorisation and Restriction of Chemicals) mandates genotoxicity testing for chemical substances based on production volume, requiring a standard information set under Annex VIII for substances exceeding 10 tonnes per year, which includes in vitro assays for gene mutations (e.g., Ames test, OECD TG 471) and chromosomal aberrations (e.g., OECD TG 473), supplemented by in vivo somatic cell tests (e.g., micronucleus assay, OECD TG 474) if in vitro results are positive.^[108] This tiered battery aligns with OECD test guidelines, promoting a stepwise strategy from screening to mechanistic confirmation, and allows adaptations for read-across or in silico predictions to minimize testing while addressing potential mutagenicity.^[109] Weight-of-evidence assessments are integral, integrating historical data and structural alerts to classify substances as genotoxic or non-genotoxic. Revisions in the 2010s enhanced these frameworks by incorporating advanced in vivo assays; for instance, the ICH S2(R1) update in 2011 endorsed the in vivo comet assay (OECD TG 489, adopted 2014) as an alternative for detecting DNA strand breaks, and the Pig-a gene mutation assay (OECD TG 470, adopted 2015) for measuring mutations in peripheral blood erythrocytes. These updates improved sensitivity for low-dose effects and integration into repeat-dose studies. In 2025, OECD issued 56 updated test guidelines, with ongoing work on adaptations for nanomaterials in genotoxicity testing, including projects to modify endpoints like the Ames and micronucleus assays to account for particle-specific interactions such as agglomeration and cellular uptake. Additionally, in September 2025, the ToxTracker assay was accepted into the OECD Test Guidelines Programme, providing a stem cell-based in vitro method to identify genotoxic compounds and their modes of action.^[110]^[111] For regulatory compliance with low-exposure genotoxins, the Threshold of Toxicological Concern (TTC) approach sets a conservative limit of 0.15 μg/person/day (equivalent to 0.0025 μg/kg body weight/day) for DNA-reactive substances without carcinogenicity data, derived from a 50% database of genotoxic carcinogens to ensure a negligible risk (1 in 10^6 lifetime cancer risk). This TTC value is applied in EFSA assessments for food contact materials, while ICH M7 uses a threshold of 1.5 μg/person/day for pharmaceutical impurities, corresponding to a 1 in 10^5 lifetime cancer risk.^[112]

Mitigation Strategies in Medicine and Industry

In medicine, dose optimization is a key strategy to minimize genotoxic risks from chemotherapeutic agents like cisplatin, where lower cumulative doses have been shown to reduce DNA damage while maintaining efficacy against tumors. Protective agents such as amifostine are administered to shield normal tissues from cisplatin-induced genotoxicity, particularly nephrotoxicity, by scavenging free radicals and inhibiting DNA cross-linking in healthy cells.^[113] Additionally, shifting toward non-genotoxic alternatives, such as immunotherapy, avoids direct DNA damage altogether; for instance, immune checkpoint inhibitors like pembrolizumab target cancer cells via T-cell activation without the mutagenic effects of traditional chemotherapy.^[114] In industrial settings, substitution of highly genotoxic solvents like benzene with less hazardous alternatives such as toluene significantly lowers exposure risks, as toluene exhibits reduced carcinogenicity and mutagenicity in occupational environments.^[115] Engineering controls, including local exhaust ventilation systems, capture airborne genotoxins at the source, preventing inhalation in chemical manufacturing and pharmaceutical production facilities.^[116] Personal protective equipment (PPE), such as nitrile gloves, closed-front gowns, and N95 respirators, provides a critical barrier during handling of genotoxic substances, with double-gloving recommended for high-risk tasks to minimize skin absorption.^[117] Ongoing monitoring through biomarkers, like micronucleus frequency in peripheral blood lymphocytes, enables early detection of genotoxic effects in exposed workers, facilitating timely interventions.^[118] Public health initiatives emphasize exposure limits, such as the OSHA permissible exposure limit (PEL) for benzene of 1 ppm as an 8-hour time-weighted average, to curb occupational and environmental genotoxic hazards.^[119] Education campaigns promote dietary avoidance of genotoxins, advising reduced consumption of processed meats containing N-nitroso compounds, which the WHO classifies as carcinogenic due to their DNA-alkylating potential.^[120] Emerging in the 2020s, AI-driven predictive modeling integrates machine learning with chemical structure data to forecast genotoxicity in drug candidates, allowing pharmaceutical developers to preemptively exclude mutagenic compounds and streamline safer design processes.^[121]

References

[1]
A Systematic Review of the Genotoxicity and Antigenotoxicity ... - NIH
Genotoxicity can be defined as destructive genetic alterations involving gene mutations, structural chromosomal aberrations, and recombination that are induced ...
[2]
Genotoxicity assessment: opportunities, challenges and ...
Jul 5, 2023 · Genotoxic substances alter the structure, information content, or segregation of DNA in different ways. 'DNA-reactive' substances primarily ...
[3]
Genotoxicity: damage to DNA and its consequences - PubMed
A genotoxin is a chemical or agent that can cause DNA or chromosomal damage. Such damage in a germ cell has the potential to cause a heritable altered trait ...
[4]
Opinion: regulatory genotoxicity: past, present and future - PMC - NIH
Apr 22, 2022 · Introduction. Regulatory genotoxicology is defined as genotoxic studies to support regulatory decision-making related to chemical safety.
[5]
[PDF] Guidance for Industry - S2B Genotoxicity - FDA
Genotoxicity tests can be defined as in vitro and in vivo tests designed to detect compounds that induce genetic damage directly or indirectly by various ...
[6]
Thresholds of Genotoxic and Non-Genotoxic Carcinogens - PMC
Genotoxic chemicals, like radiation, induce DNA damage and mutations that may lead to cancer; indeed, genotoxic chemicals used to be called “radiomimetic ...
[7]
Genetic toxicology in silico protocol - PMC
Genetic toxicology (genotoxicity) concerns the effects induced by genetic alterations that may occur in somatic and/or germ cells following exposure to a ...<|control11|><|separator|>
[8]
The Structure and Function of DNA - Molecular Biology of the Cell
The ability of each strand of a DNA molecule to act as a template for producing a complementary strand enables a cell to copy, or replicate, its genes before ...
[9]
DNA Replication - The Cell - NCBI Bookshelf - NIH
DNA replication is a semiconservative process in which each parental strand serves as a template for the synthesis of a new complementary daughter strand.DNA Polymerases · The Replication Fork · The Fidelity of ReplicationMissing: basics | Show results with:basics
[10]
Engineered Nanoparticles May Induce Genotoxicity
The mechanisms of genotoxicity are classified as either direct or indirect. Direct genotoxicity results from physical interactions with DNA, for example ...
[11]
The various aspects of genetic and epigenetic toxicology - NIH
May 22, 2017 · In genetics, genotoxicity refers to the ability of harmful substances to damage genetic information. It is often confused with mutagenicity, ...
[12]
Genotoxicity - an overview | ScienceDirect Topics
Genotoxicity is the ability of chemicals to damage the genetic information within a cell resulting in mutations, which may lead to malignancies.
[13]
Overview of genotoxic carcinogens and non-genotoxic carcinogens
The term "genotoxic carcinogen" indicates a chemical capable of producing cancer by directly altering the genetic material of target cells.
[14]
Thresholds of Genotoxic and Non-Genotoxic Carcinogens
Oct 1, 2018 · Carcinogens are currently categorized into two classes, genotoxic and non-genotoxic carcinogens, which are subject to different regulatory ...
[15]
Potential thresholds for genotoxic effects by micronucleus scoring
The concept of thresholds in genotoxicity has been open for debate in the last decades. The micronucleus (MN) test contributed to a large extent in ...
[16]
A Structure for Deoxyribose Nucleic Acid - Nature
The determination in 1953 of the structure of deoxyribonucleic acid (DNA), with its two entwined helices and paired organic bases, was a tour de force in ...<|control11|><|separator|>
[17]
Aflatoxin: A 50-Year Odyssey of Mechanistic and Translational ...
EXPERIMENTAL AFLATOXIN CARCINOGENESIS. The carcinogenic potency of AFB1 has been well established in many species of animals, including rodents, nonhuman ...
[18]
https://pmc.ncbi.nlm.nih.gov/articles/PMC3043084/
[19]
The comet assay: past, present, and future - Frontiers
Since the first report by Ostling and Johanson (1984) the comet assay has been widely used in genotoxicity testing of chemicals, in both in vitro and in vivo ...
[20]
https://www.oecd.org/chemicalsafety/risk-assessment/1948442.pdf
[21]
[PDF] The Need for Epigenotoxicity Testing* - KOPS
Apr 1, 2024 · Epigenetics contributes to GxE by modifying the accessibility of genes and thus their ability to be translated to proteins. Epigenetic ...
[22]
Mechanisms of DNA damage, repair and mutagenesis - PMC
Types of DNA damage. DNA damage can be categorized into two main classes based on its origin: endogenous and exogenous. The majority of the endogenous DNA ...
[23]
Carcinogens and DNA damage - PMC - PubMed Central
Oct 4, 2018 · Damage can be direct and genotoxic effects include DNA adducts resulting from oxidative damage, epigenetic changes and DNA strand breaks.Introduction · Table 1. Examples Of... · Types Of Dna Damage: Direct...
[24]
Experimental Adaptation of Salmonella typhimurium to Mice - PMC
With an estimated target size for auxotrophy of 2 × 105 bp (Hughes and Andersson 1997), the mutation rate per base pair per replication would be 2 × 10−9.
[25]
Alkylating Agents - Holland-Frei Cancer Medicine - NCBI Bookshelf
The alkylating agents are compounds that react with electron-rich atoms in biologic molecules to form covalent bonds. Traditionally, these agents are divided ...Missing: genotoxins | Show results with:genotoxins
[26]
Cytochromes P450 in benzene metabolism and involvement of ... - NIH
Cytochrome P450 (CYP) 2E1 was the most efficient CYP enzyme that oxidized benzene to soluble and covalently bound metabolites in rat and human liver microsomes.Missing: indirect epoxides
[27]
DNA damage in internal organs after cutaneous exposure to sulphur ...
Jul 1, 2014 · Mustard agents are potent DNA alkylating agents with mutagenic, cytotoxic and vesicant properties. They include bi-functional agents, such ...
[28]
SULFUR MUSTARD - Chemical Agents and Related Occupations
There is strong evidence that the carcinogenicity of sulfur mustard operates by a genotoxic mechanism of action that involves DNA alkylation leading to cross- ...
[29]
DNA-directed alkylating agents. 1. Structure-activity relationships for ...
Enhancement of radiosensitivity in human glioblastoma cells by the DNA N-mustard alkylating agent BO-1051 through augmented and sustained DNA damage response.
[30]
Green Tea Attenuates Benzene-Induced Oxidative Stress in Pump ...
Benzene can be enzymatically bioactivated to reactive intermediates that can lead to increased formation of reactive oxygen species (ROS). The peroxidatic ...
[31]
[PDF] Metabolism and genotoxicity of polycyclic aromatic hydrocarbons in ...
Jan 14, 2020 · They are converted by phase I enzymes, such as cytochrome P450-dependent monooxygenases (CYP450), into reactive metabolites, which then ...
[32]
[PDF] Toxicity of Polycyclic Aromatic Hydrocarbons (PAHs) | ATSDR - CSEM
Jul 1, 2009 · Studies show that certain PAH metabolites interact with DNA and are genotoxic, causing malignancies and heritable genetic damage in humans. • In ...<|separator|>
[33]
Evaluation of the Suitability of Mammalian In Vitro Assays to Assess ...
In vitro genotoxicity tests can be classified according to the mechanism they are detecting. Direct-acting agents usually cause gene mutations and can be ...
[34]
Cytome micronucleus assays with a metabolically competent human ...
One of the main problems of in vitro genotoxicity tests is the inadequate representation of drug metabolizing enzymes in most indicator cell lines which are ...Missing: challenges | Show results with:challenges
[35]
DNA damage evaluated by γH2AX foci formation by a selective ...
Two direct-acting genotoxins, methyl methanesulfonate (MMS) and N-ethyl-N ... The time and dose–responses of two indirect genotoxins, BP and AAF, were also ...
[36]
Test No. 476: In Vitro Mammalian Cell Gene Mutation Tests ... - OECD
In this test, the used genetic endpoints measure mutation at hypoxanthine-guanine phosphoribosyl transferase (HPRT), and at a transgene of xanthineguanine ...
[37]
In vitro genotoxicity testing using the micronucleus assay in cell lines ...
The OECD guideline 478 for the IVMN refers to the extensive data supporting the validity of the assay using various rodent cell lines (CHO, V79, CHL and L5178Y) ...Missing: limitations | Show results with:limitations
[38]
Evaluation of the Suitability of Mammalian In Vitro Assays to Assess ...
Feb 22, 2020 · In this review, mammalian in vitro genotoxicity assays are analyzed for their ability to detect DNA-damaging substances at limits of biological detection (LOBD)
[39]
Test No. 487: In Vitro Mammalian Cell Micronucleus Test | OECD
The in vitro micronucleus test is a genotoxicity test detecting micronuclei in cells, which may originate from chromosome fragments or whole chromosomes.Missing: HPRT SCE
[40]
Test No. 479: Genetic Toxicology: In vitro Sister Chromatid ... - OECD
The sister chromatid exchange (SCE) assay is a short-term test for the detection of reciprocal exchanges of DNA between two sister chromatids of a ...
[41]
Sister Chromatid Exchange - an overview | ScienceDirect Topics
The in vitro sister chromatid exchange test in mammalian cells was removed from the OECD test guidelines in April 2014, but this test is still continuously ...
[42]
In vitro genotoxicity testing-Can the performance be enhanced?
These include the improvement of existing tests, the development of novel tests, as well as, the establishment and exploration of approaches to optimise in ...Missing: techniques | Show results with:techniques
[43]
[PDF] Test Guideline No. 471 Bacterial Reverse Mutation Test - OECD
Jun 26, 2020 · If 2- aminoanthracene is used, each batch of S9 should also be characterised with a mutagen that requires metabolic activation by microsomal ...
[44]
[PDF] ICH guideline S2 (R1) on genotoxicity testing and data interpretation ...
This guidance replaces and combines the ICH S2A and S2B guidelines. The purpose of the revision is to optimize the standard genetic toxicology battery for ...Missing: 1980s | Show results with:1980s
[45]
The current limitations of in vitro genotoxicity testing and their ...
The standard regulatory core battery of genotoxicity tests generally includes 2 or 3 validated tests with at least one in vitro test in bacteria and one in ...Missing: techniques | Show results with:techniques
[46]
Do cytotoxicity and cell death cause false positive results in the in ...
High concentrations of test agents may cause cytotoxicity or cell death, which may give rise to false positive results in the comet assay.Do Cytotoxicity And Cell... · 2. Types Of Cytotoxicity And... · 4. Effects Of Cytotoxicity...
[47]
Genotoxicity Expert Panel review: weight of evidence evaluation of ...
1998a) is not considered valid due to the fact that there was excessive cytotoxicity (>50 ... false”) positive results in mammalian cell genotoxicity assays.
[48]
DNA Adducts: formation, biological effects, and new biospecimens ...
In this review article, we highlight the formation and biological effects of DNA adducts, and highlight our advances in human biomonitoring by mass ...<|separator|>
[49]
Test No. 486: Unscheduled DNA Synthesis (UDS) Test with ... - OECD
The purpose of the unscheduled DNA synthesis (UDS) test with mammalian liver cells in vivo is to identify substances that induce DNA repair after excision ...Missing: genotoxicity | Show results with:genotoxicity
[50]
[PDF] Test No. 488: Transgenic Rodent Somatic and Germ Cell ... - OECD
In these assays, the mutations are measured in bacterial genes (lacI, lacZ and gpt) inserted into a lambda vector. In addition, mutations can be measured in the ...
[51]
https://www.sciencedirect.com/science/article/pii/S1383571822000821
[52]
Test No. 474: Mammalian Erythrocyte Micronucleus Test | OECD
Bone marrow and/or blood cells are collected, prepared and stained. Preparations are analyzed for the presence of micronuclei. Each treated and control group ...
[53]
[PDF] Detailed Review Paper on Transgenic Rodent Mutation Assays (EN)
Jul 23, 2009 · vivo studies. In vivo genotoxicity assays offer the advantage that mammalian DNA repair processes, the status of cell cycle checkpoint genes ...
[54]
[PDF] Unclassified ENV/JM/MONO(2016)33 - OECD
Jul 13, 2016 · The purpose of genotoxicity testing is to identify chemicals that can cause genetic alterations in somatic and/or germ cells, and to use this ...
[55]
Current status and future challenges of genotoxicity OECD Test ...
Following the 3Rs' principles, it would be advised to couple this assay with the toxicokinetics studies already required by the regulatory guidelines or with ...
[56]
Redbook 2000: IV.C.1.a. Bacterial Reverse Mutation Test | FDA
Nov 2, 2017 · Reverse mutation test in either Salmonella typhimurium or Escherichia coli detects mutation in an amino acid requiring strain (histidine or tryptophan, ...
[57]
An assessment of mutagenicity of chemical substances by ... - NIH
Jul 2, 2020 · Results from the Ames test have well reproducibility (80–85%) and are consistent in comparison with results from other toxicological tests [2].
[58]
Minimum Information for Reporting on the Comet Assay (MIRCA)
Oct 26, 2020 · Introduction. The alkaline comet assay is a technically simple, sensitive assay to detect DNA damage (strand breaks and other lesions that ...
[59]
An Overview of Comet Assay Application for Detecting DNA ... - MDPI
This review discusses several research studies that employed comet assay to evaluate the environmental impact of genotoxins in aquatic environments.4. Comet Assay · 4.8. Comet Assay In Mollusca · 4.9. Comet Assay In...
[60]
[PDF] draft-test-guideline-470-mammalian-erythrocyte-pig-a-gene ... - OECD
Dec 4, 2024 · In vivo gene mutation tests, such as the Pig-a assay, are especially relevant for assessing mutagenicity because physiological factors, such as ...
[61]
The in vivo Pig-a assay: A report of the International ... - PubMed
May 1, 2015 · There is good evidence suggesting that the absence of antibody binding is the result of a mutation in the endogenous X-linked Pig-a gene, which ...
[62]
Micronuclei Detection by Flow Cytometry as a High-Throughput ...
Nov 24, 2019 · In this study, we have evaluated the advantages of using a flow cytometry-based approach testing micronucleus (MNs) induction (FCMN assay). In ...
[63]
The in vitro micronucleus assay using imaging flow cytometry and ...
May 18, 2021 · Previously, we applied imaging flow cytometry (IFC) using the ImageStream® to develop a rapid and automated MN assay based on high throughput ...
[64]
Multistage Carcinogenesis - Holland-Frei Cancer Medicine - NCBI
Multistage chemical carcinogenesis can be conceptually divided into four stages: tumor initiation, tumor promotion, malignant conversion, and tumor progression.
[65]
p53 and Ras Mutations in Cancer and Experimental Carcinogenesis
Aug 10, 2025 · These are not carcinogenic until metabolically activated to compounds known as ultimate carcinogens, which can damage DNA, leading to mutations.
[66]
Current Knowledge of Mechanisms of Carcinogenicity: Genotoxins ...
V-ras genes from Harvey and BALB murine sarcoma viruses can act as initiators of two-stage mouse skin carcinogenesis. ... Activating mutations of c-Ha-ras ...
[67]
List of Classifications - IARC Monographs
Sep 18, 2025 · IARC Monographs on the Identification of Carcinogenic Hazards to Humans · HOME · News · Meetings · Classifications · Publications · Priorities.
[68]
Role of Mutagenicity in Asbestos Fiber-Induced Carcinogenicity and ...
This article summarizes the findings from existing literature with a focus on genetic changes, specifically, mutagenicity of asbestos fibers.
[69]
AFLATOXINS (IARC Summary & Evaluation, Volume 82, 2002)
Dec 4, 2002 · Studies evaluated in Volume 56 of the IARC Monographs led to the classification of naturally occurring aflatoxins as carcinogenic to humans ( ...
[70]
(PDF) Epidemiology of Aflatoxin Exposure and Human Liver Cancer
Aug 6, 2025 · The International Agency for Research on Cancer (IARC) has designated aflatoxin as a human liver carcinogen (Wogan 2000). To minimize ...<|separator|>
[71]
[PDF] The role of genotoxicity in carcinogenesis - IARC Publications
Thus, it is not surprising that more than 90% of the known human chemical carcinogens (IARC. Group 1) are positive in convention- al short-term tests for ...
[72]
Environmental Factors Inducing Human Cancers - PMC - NIH
Up to 93% of all human cancers are non-hereditary which is caused by interaction with environmental factors. ... The mutagens and produced free radicals can be ...
[73]
Lung Carcinogenesis by Tobacco Smoke - PMC - PubMed Central
This paper will present a mechanistic framework for understanding how cigarette smoking causes lung cancer, focusing on genotoxic caricnogens and their DNA ...
[74]
Persistence of Cisplatin-Induced Mutagenicity in Hematopoietic ...
Although our data support a genotoxic mode of action for secondary leukemias related to the use of cisplatin, the risk/benefit ratio remains decidedly in favor ...
[75]
Risk of Leukemia after Platinum-Based Chemotherapy for Ovarian ...
Feb 4, 1999 · Platinum-based treatment of ovarian cancer increases the risk of secondary leukemia. Nevertheless, the substantial benefit that platinum-based treatment offers ...
[76]
Hereditary Disorders with Defective Repair of UV-Induced DNA ...
Apr 16, 2013 · There are three representative genodermatoses resulting from genetic defects in NER: xeroderma pigmentosum (XP), Cockayne syndrome (CS), and ...
[77]
Molecular mechanisms of cisplatin-induced nephrotoxicity
Mar 13, 2019 · CDDP-induced nephrotoxicity is manifested as acute kidney injury (AKI), salt or magnesium wasting and loss of urinary concentrating ability.
[78]
Tracing brain genotoxic stress in Parkinson's disease with a novel ...
Apr 15, 2022 · To develop an in vivo tool to probe brain genotoxic stress, we designed a viral proxy as a single-cell genetic sensor termed PRISM.
[79]
TP53 Mutations in Human Cancers: Origins, Consequences ... - NIH
Genetic variations in the tumor suppressor gene TP53 (OMIM #191117) contribute to human cancers in different ways. First, somatic mutations are frequent in most ...
[80]
Folate Deficiency Triggers the Abnormal Segregation of a Region ...
Jun 30, 2021 · In summary, we have demonstrated that nondisjunction of Chr2 is promoted by folate deficiency via a CG-rich TNR region (Supplementary Figure 7).Missing: germ | Show results with:germ
[81]
DNA Damage, DNA Repair, Aging, and Neurodegeneration - PMC
This article discusses our current understanding of the role of DNA repair in counteracting aging-associated disease.
[82]
Exposure to Particulate PAHs on Potential Genotoxicity and Cancer ...
This study reveals that higher exposure to PAHs increases the risk of genotoxic effects and cancer among children.
[83]
Toxins in Tobacco Smoke - Canada.ca
Jul 26, 2023 · The International Agency for Research on Cancer says cadmium is a cancer causing heavy metal found in tobacco smoke that can damage the cells ...
[84]
A comparative study of genotoxicity endpoints for women exposed to ...
Radon and its radioactive progenies are the most important source of ionizing radiation of natural origin, being classified as a Group 1 carcinogen. The aim ...<|separator|>
[85]
Occupational benzene exposure and the risk of genetic damage
Jul 15, 2020 · Genotoxicity may be a possible carcinogenic mechanism underlying the leukemic effect of benzene [3]. Epidemiological studies have shown that ...
[86]
Carcinogenic effects of long-term exposure from prenatal life to ...
Jun 10, 2025 · Moreover pesticide mixture, including glyphosate, have been found to be associated with the overall cancer, brain and other CNS cancers, and ...Missing: benzene 2020s
[87]
[PDF] Glyphosate Scientific Review Revised Draft Phase 2 Report
Jun 19, 2024 · This Glyphosate Scientific Review summarizes information on uses, usage quantities, human health impacts,.Missing: benzene | Show results with:benzene
[88]
Exposure assessment and cancer risk characterization of aflatoxin ...
Just about 4.5 billion people globally are at risk of disproportionate exposure to aflatoxins, which account for 4.6–28.2% of all cases of hepatocellular ...
[89]
Risk assessment of dietary exposures to compounds that are ...
Aug 15, 2008 · Exposures to six genotoxic carcinogens in food (acrylamide, aflatoxin ... An early estimate suggested that diet might contribute to 40% of ...Missing: genotoxins mycotoxins
[90]
Acrylamide | EFSA - European Union
For most children, fried potato products account for up to half of all dietary exposure to acrylamide with soft bread, breakfast cereals, biscuits, crackers ...
[91]
Genotoxic Effects of Exposure to Urban Traffic Related Air Pollutants ...
Oct 7, 2020 · In urban area, gaseous and particulate pollutants interact with each other, thereby enhancing the genotoxic effects on the living organisms. ...
[92]
Microplastics as emerging carcinogens - PubMed Central - NIH
Oct 8, 2025 · These particles induce harmful biological effects by chronic inflammation, oxidative stress, genotoxicity, disturbance of lipid metabolism, and ...
[93]
Microplastics as carriers of toxic pollutants: Source, transport, and ...
Feb 15, 2024 · Microplastics have been reported to absorb pollutants such as persistent organic pollutants, heavy metals, and antibiotics, leading to their bioaccumulation.Missing: genotoxin 2020s
[94]
Genotoxic Anti-Cancer Agents and Their Relationship to DNA ... - NIH
A summary of these cytotoxic agents, their mechanism of action and the ... Examples of Drugs, Mechanism of Action, Type of DNA Damage. Alkylating agents ...
[95]
Site Specific Synthesis and Polymerase Bypass of Oligonucleotides ...
Vinyl chloride (1) shares its mechanism of action with other vinyl ... Vinyl chloride—A classical industrial toxicant of new interest. Crit Rev ...
[96]
Toxicological significance of azo dye metabolism by human ...
Studies have shown that both mammalian and microbial azoreductases cleave the azo bonds of the dyes to form compounds that are potentially genotoxic. The human ...
[97]
Adverse (geno)toxic effects of bisphenol A and its analogues in ...
We investigated the adverse toxic effects of BPA and its analogues (BPS, BPAP, BPAF, BPFL, and BPC) with emphasis on their cytotoxic and genotoxic activities.
[98]
Therapy-Related Secondary Cancers - NCBI - NIH
Alkylating agents increase the risk of leukemia almost 5-fold, but that risk increases to almost 24-fold in patients receiving the highest doses. Doxorubicin, ...
[99]
Secondary Leukemia Associated with the Anti-Cancer Agent ... - NIH
Pedersen-Bjergaard reported that the risk of developing secondary leukemia increased 336-fold with etoposide doses above 2.0 g/m2 compared to doses of 2.0 g/m2 ...Missing: percentage | Show results with:percentage
[100]
From chemotherapy to biological therapy: A review of novel ...
Dec 10, 2018 · The 5-year survival of patients with tumor-infiltrating T cells (TILs) was 38%, compared with 4.5% of patients with tumors without TILs (15).
[101]
[PDF] S2(R1) - ICH
Nov 9, 2011 · GUIDANCE ON GENOTOXICITY TESTING AND. DATA INTERPRETATION FOR ... Similar principles can be applied for other established in vivo genotoxicity ...Missing: 1980s | Show results with:1980s
[102]
S2(R1) Genotoxicity Testing and Data Interpretation for ... - FDA
Apr 24, 2020 · This guidance provides standards for optimizing genetic toxicology testing and interpreting results for human pharmaceuticals, combining two ...
[103]
Guidance on Information Requirements and Chemical Safety ...
PATHFINDER. This guidance describes the information requirements under REACH with regard to substance properties, exposure, use and risk management measures ...
[104]
OECD and EU test guidelines - ECHA - European Union
REACH ... toxicity and physical-chemical properties are generated using test guidelines. These official guidelines have been approved by the OECD and EU.
[105]
Guidelines for the Testing of Chemicals - OECD
‌The OECD Guidelines for the Testing of Chemicals are a unique tool for assessing the potential effects of chemicals on human health and the environment.About The Test Guidelines · New, Updated And Corrected... · Public Consultations
[106]
Amifostine is a Nephro-Protectant in Patients Receiving Treatment ...
Feb 25, 2021 · Amifostine may be considered for primary prevention of nephrotoxicity in patients receiving cisplatin-based chemotherapy.
[107]
Interplay between the DNA Damage Response and Immunotherapy ...
Genotoxic therapies such as chemoradiation have been employed in cancer treatments for several decades, while immunotherapy is a relatively new class of cancer ...
[108]
Toluene Toxicity - StatPearls - NCBI Bookshelf - NIH
Jan 11, 2024 · Although less toxic than benzene, toluene is not without its risks. In addition to long-term exposure risks, toluene is also abused and ...Missing: alternative | Show results with:alternative
[109]
https://echa.europa.eu/support/oecd-eu-test-guidelines
[110]
PPE for Health Care Workers Who Work with Hazardous Drugs - CDC
NIOSH recommends that employers provide appropriate personal protective equipment (PPE) to protect workers who handle hazardous drugs in the workplace.
[111]
Biomonitoring of human genotoxicity induced by complex ...
The studies have been focused on DNA adduct formation, urinary metabolites, mutations and micronuclei induced by exposures to complex organic mixtures. In two ...
[112]
https://database.ich.org/sites/default/files/M7_R1_Guideline.pdf
[113]
Carcinogenicity of the consumption of red meat and processed meat
Oct 26, 2015 · Some other dietary guidelines also recommend limiting consumption of red meat or processed meat, but these are focused mainly on reducing the ...
[114]
Review of machine learning and deep learning models for toxicity ...
This review summarizes the machine learning- and deep learning-based toxicity prediction models developed in recent years.