نتایج جستجو برای: clastogens

تعداد نتایج: 95  

Journal: :Mutagenesis 2013
Javed A Bhalli Joseph G Shaddock Mason G Pearce Vasily N Dobrovolsky

Clastogens are potential human carcinogens whose detection by genotoxicity assays is important for safety assessment. Although some endogenous genes are sensitive to the mutagenicity of clastogens, many genes that are used as reporters for in vivo mutation (e.g. transgenes) are not. In this study, we have compared responses in the erythrocyte Pig-a gene mutation assay with responses in a gene m...

2014
Rina Sakai Yuji Morikawa Chiaki Kondo Hiroyuki Oka Hirofumi Miyajima Kihei Kubo Takeki Uehara

In vitro mammalian cytogenetic tests detect chromosomal aberrations and are used for testing the genotoxicity of compounds. This study aimed to identify a supportive genomic biomarker could minimize the risk of misjudgments and aid appropriate decision making in genotoxicity testing. Human lymphoblastoid TK6 cells were treated with each of six DNA damage-inducing genotoxins (clastogens) or two ...

Journal: :Mutagenesis 2011
Azeddine Elhajouji Magdalena Lukamowicz Zoryana Cammerer Micheline Kirsch-Volders

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 understanding the dose-response relationship for aneugens and clastogens. The threshold concept for aneuploidy is well accepted by the scientific community based on the data and for mechanistic reasons. The concept of threshold for clastogens is sti...

Journal: :Environmental Health Perspectives 1981
J A Heddle M F Salamone

The importance of chromosomal aberrations as a proximate cause of bone marrow toxicity is discussed. Since chemicals that can cause nondisjunction are rare, numerical aberrations (aneuploidy, polyploidy) are not ordinarily important. Many structural aberrations, however, can lead directly to cell death and so are proximate causes of toxicity when they occur. The micronucleus test which utilizes...

Journal: :Frontiers in bioscience 2017
Masayuki Mishima

Current anticancer therapy may be one of the most important exogenous sources of exposure to genotoxic agents in US, Japan, and Europe, where approximately 40-55 percent of the population is diagnosed with cancer at a certain point in their life. This review focuses on recent efforts to integrate a novel biomarker, gamma-H2AX, into anticancer drug screening to classify the mode of action (MoA) ...

2013
Lya G. Hernández Jan van Benthem George E. Johnson

Distinguishing between clastogens and aneugens is vital in cancer risk assessment because the default assumption is that clastogens and aneugens have linear and non-linear dose-response curves, respectively. Any observed non-linearity must be supported by mode of action (MOA) analyses where biological mechanisms are linked with dose-response evaluations. For aneugens, the MOA has been well char...

Journal: :Mutagenesis 1996
T Sofuni M Honma M Hayashi H Shimada N Tanaka S Wakuri T Awogi K I Yamamoto Y Nishi M Nakadate

Under the auspices of the Ministry of Health and Welfare of Japan and the Japanese Pharmaceutical Manufacturer Association, a collaborative study of the mouse lymphoma assay (MLA) was conducted by 42 Japanese laboratories and seven overseas laboratories to clarify the performance of the MLA for the detection of in vitro clastogens and spindle poisons. Twenty-one chemicals that were positive in ...

Journal: :Environmental Health Perspectives 1993
E Gebhart R Romahn A Schneider M Hoffmann D Rau H Tittelbach

Spontaneous and clastogen-induced chromosomal instability in a high-risk group (i.e, 33 patients with rectal carcinomas) was investigated using peripheral blood lymphocytes as target cells. In addition to the analysis of spontaneous and clastogen-induced chromosome aberrations, this study also included classical karyotype analysis and scoring of sister chromatid exchanges (SCE) in some of the p...

Journal: :Blood 1992
I Dokal J Bungey P Williamson D Oscier J Hows L Luzzatto

Dyskeratosis congenita (DC) is a rare inherited disorder characterized by bone marrow failure, dystrophic changes in the skin and mucous membranes, and a predisposition to malignancy. The DC locus has been mapped to Xq28. The primary defect responsible for this disease remains unknown. We have studied four patients with this disease, three from one family and one from another. In all four patie...

Journal: :Toxicology in vitro : an international journal published in association with BIBRA 2015
N Kotova N Hebert E-L Härnwall D Vare C Mazurier L Douay D Jenssen J Grawé

The induction of micronucleated reticulocytes in the bone marrow is a sensitive indicator of chromosomal damage. Therefore, the micronucleus assay in rodents is widely used in genotoxicity and carcinogenicity testing. A test system based on cultured human primary cells could potentially provide better prediction compared to animal tests, increasing patient safety while also implementing the 3Rs...

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