In this study, the aqueous extracts of fruiting bodies of Psathyrella candolleana and Agaricus bisporus were assessed in vitro for their genotoxic potential. Extracts of these 2 fungi were tested with regard to their capacity to protect genetic material against DNA damage caused by the anticancer chemotherapy drug, doxorubicin. Using chromosomal aberration, micronucleus, and comet assays, the genotoxic and genoprotective potential of these 2 fungi was assessed using P. candolleana strain RM-0861 and A. bisporus strain AB-62. Genetic damage was determined by the chromosomal aberration assay, and evaluation of oxidative damage was performed in vitro by the micronucleus test and comet assay. A significant decrease in micronucleus formation was noted in comparison with the corresponding control. None of the mushroom extract treatments in this study displayed genotoxicity or cytotoxicity. Significantly, the greatest reductions of chromosomal aberration were found with the extracts of P. condolleana for all time periods tested. The extracts tested showed a marked anticlastogenic effect against DNA damage, as evidenced by a decrease in the frequency of total breaks. The data obtained suggest that extracts of these fungi are anticlastogenic under the conditions tested. These results indicate that mushroom extracts contain bioactive compounds that may prevent oxidative DNA damage induces by doxorubicin, as measured by chromosomal aberration, comet and micronucleus assay.
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http://dx.doi.org/10.1615/IntJMedMushrooms.2018027002 | DOI Listing |
Drug Chem Toxicol
January 2025
Faculty of Medicine, Department Psychiatry, Çanakkale Onsekiz Mart University, Çanakkale, Türkiye.
Although atomoxetine, a selective norepinephrine reuptake inhibitor, is widely used in the treatment of attention-deficit/hyperactivity disorder (ADHD), there is limited data on its cytogenetic effects. This study aimed to investigate the cytotoxicity and genotoxicity of atomoxetine and . Chromosome aberration and micronucleus assays were used to analyze the genotoxic effect of atomoxetine in human peripheral blood lymphocytes under culture conditions.
View Article and Find Full Text PDFToxicol Appl Pharmacol
January 2025
Division of Pathology, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-9501, Japan.
Acetamide is a hepatocarcinogen in rats. We previously revealed that acetamide induces characteristic large micronuclei in rat liver, suggesting the possible involvement of chromosome aberrations in acetamide-induced hepatocarcinogenesis. To elucidate the mechanism of large micronuclei formation, in this study we examined time-dependent changes in rat hepatocytes after administration of acetamide.
View Article and Find Full Text PDFCurr Protoc
January 2025
Myriad Genetic Laboratories, Inc., Salt Lake City, Utah.
Balanced translocation carriers experience elevated reproductive risks, including pregnancy loss and children with anomalies due to generating chromosomally unbalanced gametes. While understanding the likelihood of producing unbalanced conceptuses is critical for individuals to make reproductive decisions, risk estimates are difficult to obtain as most balanced translocations are unique. To improve reproductive risk estimates, Drs.
View Article and Find Full Text PDFGenes Chromosomes Cancer
January 2025
Laboratory of Cancer Genetics and Tumor Biology, Translational Medicine Research Unit, Medical Research Center Oulu and Biocenter Oulu, University of Oulu, Oulu, Finland.
Myelodysplastic neoplasia with complex karyotype (CK-MDS) poses significant clinical challenges and is associated with poor survival. Detection of structural variants (SVs) is crucial for diagnosis, prognostication, and treatment decision-making in MDS. However, the current standard-of-care (SOC) cytogenetic testing, relying on karyotyping, often yields ambiguous results in cases with CK.
View Article and Find Full Text PDFInt J Mol Sci
January 2025
Department of Neurology, Centro Hospitalar Universitário de Santo António, Unidade Local de Saúde de Santo António, 4099-001 Porto, Portugal.
Chromosomal aberrations are rare but known causes of movement disorders, presenting with broad phenotypes in which dystonia may be predominant. During the investigation of such cases, chromosomal studies are not often considered as a first approach. In this article, the authors describe a family affected by a generalized form of dystonia, evolving from a focal phenotype, for which a new X chromosome large duplication was found to be the likely causative, therefore highlighting the role of such studies when facing complex movement disorders.
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