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BACKGROUND: Meat-cooking mutagens may be associated with renal cell carcinoma (RCC) risk. In the current study, the authors examined associations between meat-cooking mutagens, genetic susceptibility variants, and risk of RCC. METHODS: The authors used 659 newly diagnosed RCC cases and 699 healthy controls to investigate the association between dietary intake of meat-cooking mutagens and RCC. They examined whether associations varied by risk factors for RCC and genetic susceptibility variants previously identified from genome-wide association studies. Odds ratios and 95% confidence intervals were estimated using tertiles of intake of dietary polycyclic aromatic hydrocarbons/heterocyclic amines. RESULTS: Dietary intake of the mutagenic compounds 2-amino-3,8-dimethylimidazo-(4,5-f) quinoxaline (MeIQx) and 2-amino-1 methyl-6-phenylimidazo(4,5-b)pyridine (PhIP) were found to be significantly associated with an increased risk of RCC (odds ratios across tertiles: 1.00 [referent], 1.28 [95% confidence interval, 0.94-1.74], and 1.95 [95% confidence interval, 1.43-2.66] [P for trend <.001], respectively; and 1.00 [referent], 1.41 [95% confidence interval, 1.04-1.90], and 1.54 [95% confidence interval, 1.14-2.07] [P for trend =.02], respectively). The authors observed evidence of interactions between PhIP and RCC susceptibility variants in 2 genes: inositol 1,4,5-trisphosphate receptor, type 2 (ITPR2) (rs718314; multiplicative P for interaction = .03 and additive P for interaction =.002) and endothelial PAS domain-containing protein 1 (EPAS1) (rs7579899; additive P for interaction =.06). CONCLUSIONS: The intake of meat may increase the risk of RCC through mechanisms related to the cooking compounds MeIQx and PhIP. These associations may be modified by genetic susceptibility to RCC. Further research is necessary to understand the biological mechanisms underlying these interactions.
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Carcinoma de Células Renales/epidemiología , Neoplasias Renales/epidemiología , Carne , Mutágenos/administración & dosificación , Carcinoma de Células Renales/inducido químicamente , Carcinoma de Células Renales/etiología , Carcinoma de Células Renales/genética , Estudios de Casos y Controles , Susceptibilidad a Enfermedades , Femenino , Interacción Gen-Ambiente , Predisposición Genética a la Enfermedad , Estudio de Asociación del Genoma Completo , Genotipo , Humanos , Imidazoles/administración & dosificación , Imidazoles/envenenamiento , Neoplasias Renales/inducido químicamente , Neoplasias Renales/etiología , Neoplasias Renales/genética , Masculino , Persona de Mediana Edad , Mutágenos/envenenamiento , Quinoxalinas/administración & dosificación , Quinoxalinas/envenenamiento , Factores de Riesgo , Estados Unidos/epidemiologíaRESUMEN
OBJECTIVE: Pentachlorophenol (PCP) is characterized as likely carcinogen of lymphoma and hematopoietic neoplasm. But the carcinogenicity to human was uncertain based on population studies. A systematic review was conducted to explore two kinds of associations, one was between the workers exposed to PCP with lymphoma and hematopoietic neoplasm, the other was between childhood lymphoma and leukemia with their parents exposed to PCP. METHODS: Systematic search for epidemiologic studies was carried out and the data were collected from MEDLINE database and from the reference lists of relevant studies. Data were extracted from 20 included studies published between 1986 and 2012. RESULTS: The meta-analysis suggested a significant association between lymphoma and workers' occupational exposing to PCP, for the pooled odds ratio = 2.57 (95% confidence interval (CI) = 1.52-4.35). The subgroup analysis indicated significant association for non-Hodgkin's lymphoma, but not for Hodgkin's disease. The cohort studies also showed comparatively higher relative risk (RR) and standardized mortality ratio (SMR). Two of the cohort studies found increased RR as the cumulative exposure time added. Another cohort study discovered that the white males had significantly elevated non-Hodgkin's lymphoma mortality (SMR = 1.98, 95% CI = 1.15-3.17), and males of other races had increased leukemia mortality (SMR = 4.57, 95% CI = 1.25-11.7). For the relationship of childhood leukemia and parental exposure to PCP, three published studies suggested an increased risk of childhood leukemia because of their parental exposure to PCP at the preconception period. CONCLUSION: Our review provided the evidence that occupational exposure of workers to PCP might increase the risk of lymphoma and hematopoietic neoplasm in themselves and in their children.
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Neoplasias Hematológicas/inducido químicamente , Linfoma/inducido químicamente , Mutágenos/envenenamiento , Enfermedades Profesionales/inducido químicamente , Exposición Profesional/estadística & datos numéricos , Pentaclorofenol/envenenamiento , Adolescente , Niño , Preescolar , Femenino , Neoplasias Hematológicas/epidemiología , Humanos , Lactante , Recién Nacido , Linfoma/epidemiología , Masculino , Exposición Materna , Enfermedades Profesionales/epidemiología , Oportunidad Relativa , Exposición PaternaRESUMEN
The chlorinated solvent trichloroethylene (TCE) is a ubiquitous environmental pollutant. The carcinogenic hazard of TCE was the subject of a 2012 evaluation by a Working Group of the International Agency for Research on Cancer (IARC). Information on exposures, relevant data from epidemiologic studies, bioassays in experimental animals, and toxicity and mechanism of action studies was used to conclude that TCE is carcinogenic to humans (Group 1). This article summarizes the key evidence forming the scientific bases for the IARC classification. Exposure to TCE from environmental sources (including hazardous waste sites and contaminated water) is common throughout the world. While workplace use of TCE has been declining, occupational exposures remain of concern, especially in developing countries. The strongest human evidence is from studies of occupational TCE exposure and kidney cancer. Positive, although less consistent, associations were reported for liver cancer and non-Hodgkin lymphoma. TCE is carcinogenic at multiple sites in multiple species and strains of experimental animals. The mechanistic evidence includes extensive data on the toxicokinetics and genotoxicity of TCE and its metabolites. Together, available evidence provided a cohesive database supporting the human cancer hazard of TCE, particularly in the kidney. For other target sites of carcinogenicity, mechanistic and other data were found to be more limited. Important sources of susceptibility to TCE toxicity and carcinogenicity were also reviewed by the Working Group. In all, consideration of the multiple evidence streams presented herein informed the IARC conclusions regarding the carcinogenicity of TCE.
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Carcinógenos Ambientales/toxicidad , Neoplasias/inducido químicamente , Neoplasias/epidemiología , Solventes/toxicidad , Tricloroetileno/toxicidad , Animales , Carcinógenos Ambientales/farmacocinética , Carcinógenos Ambientales/envenenamiento , Humanos , Mutágenos/farmacocinética , Mutágenos/envenenamiento , Mutágenos/toxicidad , Factores de Riesgo , Solventes/farmacocinética , Solventes/envenenamiento , Tricloroetileno/farmacocinética , Tricloroetileno/envenenamientoRESUMEN
OBJECTIVE: Carbon monoxide (CO) exposure is still one of the leading causes of unintentional poisonings. Although its neurological sequels have been extensively studied, the knowledge about cytogenetic conse- quences still remains very limited. The aim of this study was to estimate the genotoxic potential of carbon monoxide in the course of acute poisoning. METHODS: The examined group consisted of 73 patients treated because of accidental acute CO poisoning, and 22 healthy control individuals. Poisoning severity was estimated on the basis of neurological symptoms at admission, age, duration of exposure, carboxyhemoglobin (COHb) level and blood lactate concentration. The cytochalasine-B (cytokinesis blocker) micronucleus assay (CBMN) was used to analyze the cytogenetic alterations in lymphocytes from peripheral blood of the patients. RESULTS: Intoxicated patients displayed higher numbers of micronuclei (MN) than controls. The frequency of MN depended on the age of patients, loss of consciousness, neurological symptoms at admission, and the level of carboxyhemoglobin, but did not correlate with lactate level. We also observed differences in cell responses depending on the gender. CONCLUSION: Our results confirm the presence of cytogenetic changes after carbon monoxide poisoning. Based on these data we conclude, that CO might have genotoxic potential.
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Intoxicación por Monóxido de Carbono/sangre , Intoxicación por Monóxido de Carbono/genética , Monóxido de Carbono/toxicidad , Linfocitos/patología , Micronúcleos con Defecto Cromosómico/inducido químicamente , Mutágenos/envenenamiento , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Análisis de Varianza , Monóxido de Carbono/sangre , Estudios de Casos y Controles , Proliferación Celular/genética , Femenino , Humanos , Masculino , Pruebas de Micronúcleos , Persona de Mediana Edad , Fumar/sangre , Adulto JovenRESUMEN
The electroplating industry commonly involves the use of nickel and chromium. An assessment of the genotoxic effects of these metals can be carried out by micronucleus (MN) test in buccal cells. Other nuclear anomalies (NA) observed in buccal cells viz., karyorrhexis, pyknosis and karyolysis are also the indicators of genotoxicity. The current study aims at determining the extent of genotoxic damage in relation to the duration of exposure to nickel and hexavalent chromium via micronuclei induction and other nuclear anomalies. The present investigation included 150 subjects of which 50 individuals with no history of nickel/chromium exposure (Group I) were taken as control, 50 electroplaters exposed to nickel and hexavalent chromium for duration of less than 10 years (Group II) and 50 electroplaters exposed for ≥10 years (Group III) were included. Slides of buccal cells were prepared and the frequency of MN () and NA () were calculated. ANOVA was applied to test significance. Results were considered significant at p < 0.05 and p < 0.001. Group III showed the highest MN frequency (1.08 ± 0.54, p < 0.05), karyorrhexis (20.75 ± 6.29, p < 0.05), karyolysis (3.50 ± 1.91, p < 0.001), binucleate (4.75 ± 2.75, p < 0.05) and enucleated cells (5.75 ± 1.70, p < 0.05). Significant increase in frequencies between Group II and III was found as duration of exposure increased. Plasma nickel and chromium levels were also determined which showed a positive correlation with frequency MN and other nuclear abnormalities (p < 0.01).
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Cromo/envenenamiento , Mucosa Bucal/efectos de los fármacos , Mutágenos/envenenamiento , Níquel/envenenamiento , Enfermedades Profesionales/inducido químicamente , Exposición Profesional/efectos adversos , Adulto , Análisis de Varianza , Estudios de Casos y Controles , Cromo/sangre , Daño del ADN , Galvanoplastia , Humanos , Masculino , Metalurgia , Micronúcleos con Defecto Cromosómico/inducido químicamente , Pruebas de Micronúcleos , Mucosa Bucal/citología , Níquel/sangre , Enfermedades Profesionales/sangre , Enfermedades Profesionales/genéticaRESUMEN
Hydroquinone is a phenolic metabolite of benzene, a known human carcinogen. Hydroquinone is widely used in the industry. We report a case of a 43-year-old male diagnosed with antecedent myelodysplastic syndrome and acute myeloid leukemia following 16 years of occupational exposure to hydroquinone in radiographic developer solution. Cytogenetic studies revealed aberrations in chromosome 5 and chromosome 7. We review the literature on hydroquinone as a potential cause of hematolymphatic cancers and discuss the role of hydroquinone as a genotoxic and leukemogenic agent.
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Aberraciones Cromosómicas/inducido químicamente , Hidroquinonas/envenenamiento , Leucemia Mieloide Aguda/inducido químicamente , Mutágenos/envenenamiento , Síndromes Mielodisplásicos/inducido químicamente , Enfermedades Profesionales/inducido químicamente , Exposición Profesional/efectos adversos , Adulto , Animales , Benceno/metabolismo , Benceno/envenenamiento , Benceno/toxicidad , Cromosomas Humanos Par 5 , Cromosomas Humanos Par 7 , Humanos , Hidroquinonas/metabolismo , Hidroquinonas/toxicidad , Leucemia Mieloide Aguda/genética , Masculino , Ratones , Mutágenos/metabolismo , Mutágenos/toxicidad , Síndromes Mielodisplásicos/genética , Enfermedades Profesionales/genética , RatasRESUMEN
OBJECTIVES: The aim of this study was to investigate the cyto- and genotoxicity of nanocomposites (NCs) and generation of reactive oxygen species (ROS) as a result of particle-cell interactions. MATERIALS AND METHODS: Titanium dioxide (TiO(2)-Ag) and ion-exchange resin (Res-Ag), both coated with silver (Ag), were examined. The murine macrophage J774A.1 cells were incubated in vitro with NC at different concentrations for 24 h. Cytotoxicity was analyzed by the methylthiazolyldiphenyl-tetrazolium bromide reduction test (MTT reduction test). ROS generation was assessed by incubation of cells with dichlorodihydrofluorescein diacetate (DCF) and flow cytometry. DNA damage was detected by comet assay and included single-strand breaks (SSB), alkali-labile sites (ALS) and oxidative DNA damage after formamidopyrimidine glycosylase (FPG) treatment. The tail moment was used as an indicator of DNA damage. RESULTS: TiO(2)-Ag was not cytotoxic up to 200 µg/ml, whereas IC(50) for Res-Ag was found to be 23 µg/ml. Intracellular ROS levels were elevated after 4 h of exposure to Res-Ag at the concentration of 50 µg/ml. Both types of NC induced fragmentation of DNA strands, but only one of the composites caused damage to purine bases. TiO(2)-Ag induced SSB of DNA at concentrations of 10 and 5 µg/ml. For Res-Ag, a concentration-dependent increase in tail moments was observed. CONCLUSIONS: Silver-coated nanocomposites (both TiO(2)-Ag and Res-Ag) may cause genotoxic effects in murine macrophages J774A.1. Res-Ag increased generation of ROS which suggested that toxicity of Res-Ag in murine macrophages is likely to be mediated through oxidative stress. This paper will support industry and regulators alike in the assessment of hazards and risks and methods for their mitigation at the earliest possible stage in material and product development.
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Citotoxinas/análisis , Citotoxinas/envenenamiento , Mutágenos/análisis , Mutágenos/envenenamiento , Nanoestructuras/envenenamiento , Plata/efectos adversos , Plata/metabolismo , Industria Textil , Bioensayo/métodos , Citotoxinas/genética , Daño del ADN/efectos de los fármacos , Humanos , Exposición Profesional/efectos adversos , Exposición Profesional/análisis , Polonia , Especies Reactivas de Oxígeno/análisisRESUMEN
Cigarillos (aka little cigars) have been increasing in popularity unlike cigarettes; but relatively little is known about the toxicology of the mainstream smoke (MSS) from such products. Therefore, the objective of this work was to compare the toxicological properties of the MSS (Health Canada Intensive smoking conditions) from a range of cigarillo products with the toxicological properties of MSS of cigarettes. Three in vitro assays were used to evaluate the toxicities of the MSS total particulate matter (TPM): (1) mutagenicity using Ames assay with Salmonella strains TA98 and TA100 with S9 metabolic activation (+S9); (2) cytotoxicity using the Neutral Red Uptake (NRU) assay with CHO (Chinese Hamster Ovary) cells; and (3) genotoxicity using the micronucleus assay with CHO cells and short-term exposures (3-h ± S9). The Ames assay (TA100+S9) and the NRU assay were also applied to the gas/vapour phase of the MSS that passed through the Cambridge pad. On a per-milligram-nicotine basis, the preferred way of comparing toxicities of different types of tobacco products, the MSS from cigarillos was not less toxic, and in some cases more toxic (TPM fraction TA98+S9, NRU), than the MSS from cigarettes. Thus, our findings support our prior work on smoke mutagenicity that showed MSS from cigarillos was not less toxic than MSS from cigarettes.
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Mutágenos/análisis , Nicotiana/química , Nicotina/análisis , Humo/análisis , Fumar/efectos adversos , Animales , Células CHO , Canadá , Cricetinae , Humanos , Pruebas de Micronúcleos/métodos , Pruebas de Mutagenicidad/métodos , Mutágenos/envenenamiento , Mutágenos/toxicidad , Rojo Neutro/análisis , Rojo Neutro/envenenamiento , Rojo Neutro/toxicidad , Nicotina/envenenamiento , Nicotina/toxicidad , Material Particulado/análisis , Material Particulado/envenenamiento , Material Particulado/toxicidad , Salmonella/efectos de los fármacosRESUMEN
Hexavalent chromium Cr (VI) used in shielded metal arc welding is widely recognized to act as a carcinogen, mutagen and teratogen. The carcinogenic potential of metals is a major issue in defining human health risk from exposure. Hence in the present investigation, 66 welders and 60 control subjects with similar mean ages, smoking prevalences and alcohol consumption were enrolled for DNA damage analysis of buccal cells by micronucleus (MN) and comet assay. Welders showed a significant increase in micronucleated cells compared to controls and a larger mean comet tail length. The current study thus suggested that chronic occupational exposure to Cr (VI) during welding could lead to increased level of DNA damage. Understanding the complexity of the relationships between exposure, basal DNA damage and MN frequencies requires larger scale studies and application of complementary biomarkers.
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Cromo/envenenamiento , Daño del ADN , Metales/envenenamiento , Enfermedades Profesionales/inducido químicamente , Exposición Profesional/efectos adversos , Soldadura , Adulto , Consumo de Bebidas Alcohólicas/efectos adversos , Carcinógenos , Humanos , Masculino , Pruebas de Micronúcleos/métodos , Persona de Mediana Edad , Mucosa Bucal/metabolismo , Mutágenos/envenenamiento , Fumar/efectos adversos , Adulto JovenRESUMEN
INTRODUCTION: Exposure to anesthetics in the health environment may entail a health risk for patients and operating room personnel. Knowing the effects of anesthetic agents on genetic material could be a valuable basic support for anesthesia care providers to improve treatment performance, increase patient safety and reduce the risks for patients and staff in the operating room. AREAS COVERED: Relevant literature was identified using MEDLINE, CINAHL® and Cochrane Library databases. Over 200 abstracts for articles published from 1980 to 2010 were examined. Original articles were reviewed and relevant citations from these articles were also considered. EXPERT OPINION: Despite some conflicting results, the current available data indicate that exposure to anesthetics, especially nitrous oxide and halogenated agents, is associated with general and genotoxic risks, whereas intravenous agents, such as propofol and its metabolites are not associated with genotoxic effects. Moreover, given that different anesthetic drugs are used in combination it is, thus, very difficult to understand whether the observed effects or absence of effects are due to an individual agent action or linked to a synergy action of different anesthetics involved. Further clinical and experimental evidence is warranted.
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Anestésicos/envenenamiento , Mutágenos/envenenamiento , Exposición Profesional/efectos adversos , Anestesiología , Anestésicos/toxicidad , Animales , Humanos , Mutágenos/toxicidad , Quirófanos , Recursos HumanosRESUMEN
Forty-one volunteers (male non-smokers) were exposed to formaldehyde (FA) vapours for 4 h/day over a period of five working days under strictly controlled conditions. For each exposure day, different exposure concentrations were used in a random order ranging from 0 up to 0.7 p.p.m. At concentrations of 0.3 and 0.4 p.p.m., four peaks of 0.6 or 0.8 p.p.m. for 15 min each were applied. During exposure, subjects had to perform bicycle exercises (â¼80 W) four times for 15 min. Blood samples, exfoliated nasal mucosa cells and nasal biopsies were taken before the first and after the last exposure. Nasal epithelial cells were additionally sampled 1, 2 and 3 weeks after the end of the exposure period. The alkaline comet assay, the sister chromatid exchange test and the cytokinesis-block micronucleus test were performed with blood samples. The micronucleus test was also performed with exfoliated nasal mucosa cells. The expression (mRNA level) of the glutathione (GSH)-dependent formaldehyde dehydrogenase (FDH, identical to alcohol dehydrogenase 5; ADH5; EC 1.2.1.46) was measured in blood samples by quantitative real-time reverse transcription-polymerase chain reaction with TaqMan probes. DNA microarray analyses using a full-genome human microarray were performed on blood samples and nasal biopsies of selected subgroups with the highest FA exposure at different days. Under the experimental conditions of this study, inhalation of FA did not lead to genotoxic effects in peripheral blood cells and nasal mucosa and had no effect on the expression of the FDH gene. Inhalation of FA did also not cause alterations in the expression of genes in a microarray analysis with nasal biopsies and peripheral blood cells.
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Formaldehído/envenenamiento , Regulación de la Expresión Génica/efectos de los fármacos , Mutágenos/envenenamiento , Hipersensibilidad Respiratoria/genética , Biopsia , Ensayo Cometa , Formaldehído/efectos adversos , Formaldehído/sangre , Perfilación de la Expresión Génica , Humanos , Exposición por Inhalación , Masculino , Micronúcleos con Defecto Cromosómico/efectos de los fármacos , Pruebas de Mutagenicidad , Mucosa Nasal/efectos de los fármacos , Mucosa Nasal/patología , Hipersensibilidad Respiratoria/sangre , Intercambio de Cromátides Hermanas/efectos de los fármacos , Factores de TiempoRESUMEN
Carcinogenic aromatic amines are widespread and need to be regulated. Genotoxic and non-genotoxic effects are both necessary for tumor development. The common mode of action includes metabolic activation, the reaction of metabolites with nucleic acids and cellular macromolecules as well as toxic effects. The dose-response relationship of irreversible DNA damage is linear down to background concentrations and a no-effect level (NEL) cannot be defined. The dose-response relationships of reversible toxic effects are often non-linear and have been used to derive no-observed adverse effect levels (NOAEL). However, this procedure does not account for background exposure, the activity of structurally related, and those structurally unrelated chemicals which compete for the same biochemical systems. Fixed limit values for acceptable risk are therefore unacceptably uncertain. The perspective should change from "risk" to the "contribution to risk". The ALARA principle (as low as reasonably achievable) is part of such an approach. It does not say how much exposure is acceptable. Scientific risk assessment and risk management should be kept distinct and the input of scientific data and expert judgement documented.
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Aminas/envenenamiento , Hidrocarburos Aromáticos/envenenamiento , Mutágenos/envenenamiento , Neoplasias/inducido químicamente , Aminas/química , Animales , Daño del ADN , Exposición a Riesgos Ambientales/análisis , Exposición a Riesgos Ambientales/prevención & control , Humanos , Hidrocarburos Aromáticos/química , Mutágenos/química , Neoplasias/genética , Medición de Riesgo , Relación Estructura-ActividadRESUMEN
OBJECTIVE: To evaluate the variation of some biomarkers related to the level of enzymatic activity dependent on the different polymorphisms. METHODS: We studied 27 butadiene-exposed workers and 37 controls using different biomarkers of the genotoxic effect. The genotypes were determined using polymerase chain reaction and restriction fragment length polymorphism-polymerase chain reaction techniques; the subjects were assigned to a specific group based on the microsomal epoxide hydrolase (mEH) activity predicted by their genotype (low, intermediate, high). RESULTS: The studied biomarkers were not able to discriminate between exposed and control individuals, but sister chromatid exchange (SCE) and high frequency cells were influenced by smoking habits. Smokers having fast microsomal epoxide hydrolase activity showed higher SCE frequency (7.61) respect to those presenting intermediate (5.86) or slow (6.65) enzymatic activity. CONCLUSIONS: On the basis of these results, can we suppose the existence of an "intermediate genotype" advantage (at least for induction of SCE)?
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Butadienos/farmacocinética , Mutágenos/farmacocinética , Exposición Profesional/efectos adversos , Polimorfismo Genético , Adulto , Biomarcadores , Butadienos/administración & dosificación , Butadienos/metabolismo , Butadienos/envenenamiento , Análisis Citogenético , Humanos , Inactivación Metabólica , Masculino , Persona de Mediana Edad , Datos de Secuencia Molecular , Mutágenos/administración & dosificación , Mutágenos/metabolismo , Mutágenos/envenenamiento , Reacción en Cadena de la Polimerasa , Intercambio de Cromátides Hermanas , Adulto JovenRESUMEN
In 2003, we examined the chromosomes of grass voles at an illegal dumpsite at the Aomori-lwate prefectural boundary. In subsequent years, from 2003-2006, we surveyed the chromosomes of four species of small mammals, namely, the Japanese grass vole (Microtus montebelli), the large Japanese field mouse (Apodemus speciosus), the small Japanese field mouse (A. argenteus), and the greater Japanese shrew mole (Urotrichus talpoides). Each annual survey revealed, both on a yearly basis and during the entire period in question, that the frequencies of breaks and gaps in chromosomes of M. montebelli were significantly higher at the dumpsite than on the outskirts and in controls, suggesting that grass voles at the dumpsite have been subject to continuous genotoxic effects since the establishment of the dumpsite. We also ascertained that grass voles are much more susceptible to chromosomal damage than field mice and shrew moles, which had very low levels of chromosomal aberrations at the dumpsite, on the outskirts of the dumpsite, and in controls. Our four-year survey revealed two variants of M. montebelli from the dumpsite with M6 fission (2n=31), two variants of A. speciosus from the outskirts with XO monosomy (2n=47, XO), and a variant of A. speciosus from the dumpsite with situs inversus. Our analysis confirms our previously proposed hypothesis that M. montebelli might be useful as an indicator species for genotoxic assessment of below-ground pollution by industrial waste at illegal dumpsites.
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Aberraciones Cromosómicas/inducido químicamente , Residuos Peligrosos , Mamíferos/genética , Mutágenos/envenenamiento , Animales , Arvicolinae , Japón , Cariotipificación , Masculino , Ratones , Topos , MurinaeRESUMEN
Employees in the footwear manufacturing industry are routinely exposed to complex mixtures of solvents used in cleaning and as diluents in glues, primers, and degreasers. The objective of this study was to determine the genotoxic effects in a group of footwear-workers occupationally exposed to solvent-based adhesive and solutions containing organic solvents, mainly toluene. Peripheral blood and buccal cells samples were collected from 39 footwear-workers (31 males and 8 females) and 55 controls (44 males and 11 females). As biomarker of exposure, we obtained data on hippuric acid (HA), the main metabolite of toluene in urine, and DNA damage detected by the Comet assay in blood cells. Micronucleus frequencies in binucleated lymphocytes (BNMN) and in epithelial buccal cells (EBCMN) were analyzed as biomarkers of effect, while polymorphisms in genes GSTT1, GSTM1, GSTP1, CYP1A1, and CYP2E1 were used as susceptibility biomarkers. Results of HA and Comet assay showed statistical increased values amongst footwear-workers relative to controls (P < or = 0.001). No differences were observed in BNMN and EBCMN frequencies between the groups, but a correlation test revealed that age was significantly associated with BNMN frequency in both control (r(s)=0.290; P < or = 0.05) and exposed groups (r(s)=0.674; P < or = 0.001). Regarding the results on genetic polymorphisms, GSTM1 null subjects from the control group showed a significant increase in EBCMN frequency relative to GSTM1 non-null subjects (P < or = 0.05). A significant increase in DNA damage detected by Comet assay in leukocytes was obtained for GSTP1 Ile/Val or Val/Val individuals from the exposed group relative to those with GSTP1 Ile/Ile (P < or = 0.05), especially in younger subjects (P < or = 0.01), and a suggestion of interaction with CYP2E1 polymorphism was found. In confirmation of these data, stepwise multiple regression analyses for selecting between the different independent variables showed that about 25% of levels of the DNA damage in footwear-worker can be associated with genetic polymorphisms in GSTP1 and CYP2E1 (P=0.006, F=5.876).
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Daño del ADN , Mutágenos/envenenamiento , Exposición Profesional/efectos adversos , Tolueno/envenenamiento , Adulto , Biomarcadores/orina , Brasil , Ensayo Cometa , Citocromo P-450 CYP1A1/genética , Citocromo P-450 CYP1A1/metabolismo , Citocromo P-450 CYP2E1/genética , Citocromo P-450 CYP2E1/metabolismo , ADN/genética , ADN/metabolismo , Femenino , Predisposición Genética a la Enfermedad , Glutatión Transferasa/genética , Glutatión Transferasa/metabolismo , Hemoglobinas/metabolismo , Hipuratos/orina , Humanos , Masculino , Materiales Manufacturados , Pruebas de Micronúcleos , Mutágenos/farmacocinética , Reacción en Cadena de la Polimerasa , Polimorfismo Genético/efectos de los fármacos , Polimorfismo Genético/fisiología , Zapatos , Solventes/farmacocinética , Solventes/envenenamiento , Tolueno/farmacocinéticaRESUMEN
After the accident involving the oil tanker Prestige in November 2002 near 63,000 tons of heavy oil reached Galician coast (Northwest of Spain). This unleashed a large movement of volunteers to collaborate in several cleaning tasks. The aim of this study was to determine whether handling of Prestige oil-contaminated birds during autopsies and cleaning may have resulted in genotoxic damage. We have also evaluated the possible influence of DNA repair genetic polymorphisms (XRCC1 codons 194 and 399, XRCC3 codon 241 and APE1 codon 148) on susceptibility to the genotoxic effects evaluated. Exposure levels were analysed by determining volatile organic compounds in air samples. Peripheral blood samples were obtained from 34 exposed and 35 controls, and comet assay and micronucleus (MN) test were carried out. Genotyping was performed following PCR-RFLP procedures. Results obtained have shown significantly higher DNA damage, but not cytogenetic damage, in exposed individuals than in controls, related to time of exposure. Among exposed individuals, carriers of the variant alleles XRCC1 399Gln and APE1 148Glu have shown altered DNA damage with regard to wild-type homozygotes, suggesting exposure-genotype interactions. No effect of the DNA repair genetic polymorphisms analysed was observed in the MN test.
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Daño del ADN , Mutágenos/envenenamiento , Exposición Profesional , Petróleo/envenenamiento , Adulto , Animales , Aves , Ensayo Cometa , ADN-(Sitio Apurínico o Apirimidínico) Liasa/genética , Proteínas de Unión al ADN/genética , Contaminantes Ambientales/envenenamiento , Femenino , Humanos , Masculino , Aceites Volátiles/envenenamiento , Polimorfismo Genético , Proteína 1 de Reparación por Escisión del Grupo de Complementación Cruzada de las Lesiones por Rayos XRESUMEN
We collected tissues from herring gulls (Larus argentatus) nesting within and outside of the Great Lakes basin. Genotoxin exposure was assessed as fluorescent aromatic compounds (FACs) in bile and SOS Chromotest-inducing activity in muscle extracts. We determined whether these exposures were associated with decreased erythrocyte DNA strand length and/or induction of hepatic ethoxyresorufin-O-deethylase (EROD) activity. FACs were detected in all bile samples. Most muscle extracts produced a positive or marginal SOS response in the presence of S9. SOS induction potentials were strongly associated with dietary trophic level. The median molecular length of DNA isolated from erythrocytes for 14 of 17 adult and 10 of 11 prefledgling collections was reduced compared to the modal class for their respective age group suggesting widespread DNA damage. DNA damage was greatest in gulls from Saginaw Bay, Lake Huron. Median EROD activity in both adults and prefledglings from remote locations was significantly lower than that of gulls from the lower Great Lakes and was not associated with concentrations of benzo[a]pyrene (B[a]P)-like FACs. Our results indicate Great Lakes herring gulls were exposed to genotoxins and Ah-receptor activating agents in biologically significant concentrations in the early 1990s. These agents appear to be persistent bioaccumulative compounds and/or their metabolites.
Asunto(s)
Charadriiformes/genética , Citocromo P-450 CYP1A1/metabolismo , Daño del ADN , Mutágenos/envenenamiento , Contaminantes Químicos del Agua/envenenamiento , Animales , Charadriiformes/fisiología , Citocromo P-450 CYP1A1/efectos de los fármacos , Eritrocitos , Great Lakes Region , Músculo Esquelético/química , Músculo Esquelético/enzimología , Distribución TisularRESUMEN
The two major causes of bladder cancer have been recognised to be cigarette smoke and occupational exposure to arylamines. These compounds are present both in tobacco smoke and in the dyes used in textile production. Aromatic amines suffer oxidative metabolism via P450 cytochrome CYP1A2, and detoxification by the polymorphic NAT2. The aim of the present work was to assess the association between occupational-derived exposure to mutagens and CYP1A2 or NAT2 activity. This cross-sectional study included 117 textile workers exposed to dyes and 117 healthy controls. The urinary mutagenicity was determined in 24 h urine using TA98 Salmonella typhimurium strain with microsomal activation S9 (MIS9) or incubation with beta-glucuronidase (MIbeta). Urinary caffeine metabolite ratios: AFMU+1X+1U/17U, and AFMU/AFMU+1X+1U were calculated to assess CYP1A2 and NAT2 activities, respectively. The results show that workers present a strikingly higher urine mutagenicity than controls (p<0.0001), despite the implementation of the new restrictive norms forbidding the industrial use of the most carcinogenic arylamines. Neither NAT2 nor CYP1A2 activity had any effect on the markers of internal exposure to mutagens, since no significant differences were observed when the urinary mutagenicity of slow and fast acetylators (p>0.05) was compared, and the urinary mutagenicity was not significantly associated with the CYP1A2 activity marker (r=0.04 and r=-0.01 for MIS9 and MIbeta, respectively). This study clearly indicates the need for further protective policies to minimise exposure to the lowest feasible limit in order to avoid unnecessary risks.
Asunto(s)
Arilamina N-Acetiltransferasa/metabolismo , Citocromo P-450 CYP1A2/metabolismo , Exposición Profesional/análisis , Industria Textil , Adulto , Cafeína/metabolismo , Cafeína/orina , Estudios Transversales , Humanos , Persona de Mediana Edad , Análisis Multivariante , Mutágenos/envenenamiento , Exposición Profesional/efectos adversos , FumarRESUMEN
Polycyclic aromatic hydrocarbons (PAHs) such as benzo[a]pyrene (BaP) are widespread air contaminants released by transportation vehicles, power generation, and other combustion sources. Experimental evidence indicates that the developing fetus is more susceptible than the adult to carcinogenic effects of PAHs, although laboratory studies in rodents suggest that the dose to fetal tissues is an order of magnitude lower than that to maternal tissues. To assess fetal versus adult susceptibility to PAHs and environmental tobacco smoke (ETS), we compared carcinogen-DNA adducts (a biomarker associated with increased cancer risk) and cotinine (a biomarker of tobacco smoke exposure) in paired blood samples collected from mothers and newborns in New York City. We enrolled 265 nonsmoker African-American and Latina mother-newborn pairs in New York City between 1997 and 2001 (estimated average ambient air BaP concentrations < 0.5 ng/m3). Despite the estimated 10-fold lower fetal dose, mean levels of BaP-DNA adducts as determined by high-performance liquid chromatography-fluorescence were comparable in paired New York City newborn and maternal samples (0.24 adducts per 10(8) nucleotides, 45% of newborns with detectable adducts vs. 0.22 per 10(8) nucleotides, 41% of mothers with detectable adducts). However, by the Wilcoxon signed-rank test, the levels in newborns were higher (p = 0.02). Mean cotinine was higher in newborns than in mothers (1.7 ng/mL, 47% detectable vs. 1.28 ng/mL, 44% detectable). Consistent with our prior study in a Caucasian Polish population, these results indicate increased susceptibility of the fetus to DNA damage and reduced ability to clear ETS constituents. The findings have implications for risk assessment, given the need to protect children as a sensitive subset of the population.