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Department of Pharmacology, University of Texas Medical School, Houston, Texas 77025 [P. S.], and Institute of Environmental Medicine, New York University Medical Center, New York, New York 10016 [K. C., M. C.]
Chromosomal aberrations were studied in Chinese hamster ovary cells and in C3H10T
cells following treatment with NiCl2, crystalline NiS, and CaCrO4. All three compounds caused an increase in chromosomal aberrations in a concentration- and time-dependent fashion. The chromosomal aberrations induced by NiCl2, and crystalline NiS occurred predominantly in heterochromatic regions of the chromosomes. Additionally, treatment of cells with crystalline NiS and to a smaller extent long-term treatment with NiCl2 caused a preferential effect on the condensation state of the heterochromatic long arm of the X-chromosome in hamster cells. In contrast, treatment of cells with CaCrO4 did not induce aberrations preferentially in heterochromatin. These results are interesting because nickel(II), which is thought to be the ultimate carcinogen of nickel compounds, binds poorly to DNA, is weakly mutagenic, but induces chromosome damage, probably because of its interaction with nuclear proteins in heterochromatin. Chromate binds to DNA, is mutagenic, and interacts with chromatin randomly.
1 Primary support for this work was provided by Grant R812127
2 To whom requests for reprints should be addressed, at Institute of Environmental Medicine, New York University Medical Center, 550 First Ave., New York, NY 10016.
Received 6/10/86.
Revised 9/19/86. Revised 12/11/86.
Accepted 1/12/87.
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Activation of JNK, p38 and ERK mitogen-activated protein kinases by chromium(VI) is mediated through oxidative stress but does not affect cytotoxicity
Carcinogenesis,
August 1, 2000;
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