Hexavalent chromium [Cr(VI)] is a potent human carcinogen found in the workplace of more than 0.5 million individuals in the US. Environmental exposure to Cr(VI) also represents a significant public health concern due to the presence of this metal in drinking water for millions of US households and at many Superfund toxic sites. Intracellular reduction of Cr(VI) results in the formation of a wide assortment of DNA lesions, including several forms of Cr-DNA adducts. We have previously found that Cr-DNA binding was responsible for all mutagenic and genotoxic effects generated by direct metabolism of Cr(VI) with its main biological reducers. The genotoxicity of Cr-DNA adducts was unexpected considering their very weak duplex-distorting properties reflecting attachment of Cr atom to the DNA phosphate group. Cr(VI) also causes very toxic, cancer-promoting DNA double-strand breaks (DSB) that is detectable at environmentally relevant Cr(VI) doses and poorly repaired. This application, which is built on our previously published findings and new preliminary data, is designed to investigate a mechanism of DSB formation via toxic DNA repair of Cr-DNA adducts. The proposed studies aim to identify specific forms of Cr-DNA damage that trigger toxic DNA repair and DSB formation, characterize nuclease activities involved in DNA strand cleavage and determine genomic host-spots for DNA breakage and DNA repair processes. A successful completion of this work can help identify toxicologically important biomarkers of Cr(VI) exposure and high-risk genomic sites that can be used for monitoring of genetic damage in exposed populations.

Public Health Relevance

Hexavalent chromium is a widespread environmental and occupational carcinogen associated with major public concerns. This work is investigating how chromium-6 causes breakage of both DNA strands, which is the most dangerous form of DNA damage. The completion of the proposed work could lead to the identification of biomarkers of genetic injury that can improve risk assessment for this important toxic metal.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES008786-18
Application #
9043879
Study Section
Special Emphasis Panel (ZRG1-DKUS-C (90))
Program Officer
Tyson, Frederick L
Project Start
1997-08-01
Project End
2020-01-31
Budget Start
2016-02-01
Budget End
2017-01-31
Support Year
18
Fiscal Year
2016
Total Cost
$365,625
Indirect Cost
$140,625
Name
Brown University
Department
Pathology
Type
Schools of Medicine
DUNS #
001785542
City
Providence
State
RI
Country
United States
Zip Code
02912
Luczak, Michal W; Zhitkovich, Anatoly (2018) Monoubiquitinated ?-H2AX: Abundant product and specific biomarker for non-apoptotic DNA double-strand breaks. Toxicol Appl Pharmacol 355:238-246
Krawic, Casey; Zhitkovich, Anatoly (2018) Toxicological Antagonism among Welding Fume Metals: Inactivation of Soluble Cr(VI) by Iron. Chem Res Toxicol 31:1172-1184
Krawic, Casey; Luczak, Michal W; Zhitkovich, Anatoly (2017) Variation in Extracellular Detoxification Is a Link to Different Carcinogenicity among Chromates in Rodent and Human Lungs. Chem Res Toxicol 30:1720-1729
Luczak, Michal W; Zhitkovich, Anatoly (2017) Nickel-induced HIF-1? promotes growth arrest and senescence in normal human cells but lacks toxic effects in transformed cells. Toxicol Appl Pharmacol 331:94-100
Luczak, Michal W; Green, Samantha E; Zhitkovich, Anatoly (2016) Different ATM Signaling in Response to Chromium(VI) Metabolism via Ascorbate and Nonascorbate Reduction: Implications for in Vitro Models and Toxicogenomics. Environ Health Perspect 124:61-6
Sawant, Akshada; Kothandapani, Anbarasi; Zhitkovich, Anatoly et al. (2015) Role of mismatch repair proteins in the processing of cisplatin interstrand cross-links. DNA Repair (Amst) 35:126-36
DeLoughery, Zachary; Luczak, Michal W; Ortega-Atienza, Sara et al. (2015) DNA double-strand breaks by Cr(VI) are targeted to euchromatin and cause ATR-dependent phosphorylation of histone H2AX and its ubiquitination. Toxicol Sci 143:54-63
DeLoughery, Zachary; Luczak, Michal W; Zhitkovich, Anatoly (2014) Monitoring Cr intermediates and reactive oxygen species with fluorescent probes during chromate reduction. Chem Res Toxicol 27:843-51
Morse, Jessica L; Luczak, Michal W; Zhitkovich, Anatoly (2013) Chromium(VI) causes interstrand DNA cross-linking in vitro but shows no hypersensitivity in cross-link repair-deficient human cells. Chem Res Toxicol 26:1591-8
Luczak, Michal W; Zhitkovich, Anatoly (2013) Role of direct reactivity with metals in chemoprotection by N-acetylcysteine against chromium(VI), cadmium(II), and cobalt(II). Free Radic Biol Med 65:262-269

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