DNA Double-Strand Breaks Induced in Human Cells by Twelve Metallic Species: Quantitative Inter-Comparisons and Influence of the ATM Protein
Autor: | Larry Bodgi, Laurène Sonzogni, Sandrine Pereira, Béatrice Fervers, Laurent Charlet, Muriel Viau, Clément Devic, Nicolas Foray, Mélanie L. Ferlazzo, Adeline Granzotto, Elise Berthel |
---|---|
Rok vydání: | 2021 |
Předmět: |
Chromium
Radiobiology DNA Repair Iron Metal toxicity Genotoxic Stress Ataxia Telangiectasia Mutated Proteins metal carcinogenesis Microbiology Biochemistry Article Metal 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Nickel Humans DNA double-strand breaks DNA Breaks Double-Stranded Molecular Biology Carcinogen 030304 developmental biology 0303 health sciences metal toxicity fungi QR1-502 Zinc chemistry Lead Metals 030220 oncology & carcinogenesis visual_art ATM Toxicity Biophysics visual_art.visual_art_medium Metal Carcinogenesis DNA Copper Palladium Aluminum Cadmium |
Zdroj: | Biomolecules Volume 11 Issue 10 Biomolecules, Vol 11, Iss 1462, p 1462 (2021) |
ISSN: | 2218-273X |
Popis: | Despite a considerable amount of data, the molecular and cellular bases of the toxicity due to metal exposure remain unknown. Recent mechanistic models from radiobiology have emerged, pointing out that the radiation-induced nucleo-shuttling of the ATM protein (RIANS) initiates the recognition and the repair of DNA double-strand breaks (DSB) and the final response to genotoxic stress. In order to document the role of ATM-dependent DSB repair and signalling after metal exposure, we applied twelve different metal species representing nine elements (Al, Cu, Zn Ni, Pd, Cd, Pb, Cr, and Fe) to human skin, mammary, and brain cells. Our findings suggest that metals may directly or indirectly induce DSB at a rate that depends on the metal properties and concentration, and tissue type. At specific metal concentration ranges, the nucleo-shuttling of ATM can be delayed which impairs DSB recognition and repair and contributes to toxicity and carcinogenicity. Interestingly, as observed after low doses of ionizing radiation, some phenomena equivalent to the biological response observed at high metal concentrations may occur at lower concentrations. A general mechanistic model of the biological response to metal exposure based on the nucleo-shuttling of ATM is proposed to describe the metal-induced stress response and to define quantitative endpoints for toxicity and carcinogenicity. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |