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Arsenite-induced Cdc25C degradation is through the KEN-box and ubiquitin-proteasome pathway.

Chen F; Zhang Z; Bower J; Lu Y; Leonard SS; Ding M; Castranova V; Piwnica-Worms H; Shi X

Proc Natl Acad Sci USA 2002 Feb; 99(4):1990-1995

https://doi.org/10.1073/pnas.032428899

20023001

Arsenite is a known human carcinogen that induces tumorigenesis through either a genotoxic or an epigenetic mechanism. In this study, the effect of arsenite on cell cycle regulation and the mechanisms that contribute to this effect were investigated. Treatment of the cells with arsenite suppressed cell proliferation and reduced cell viability in a dose- or time-dependent manner. Analysis of cell cycle profile and cell cycle regulatory proteins indicated that arsenite arrested the cell cycle at G2/M phase, partially through induction of cell division cycle 25 (Cdc25) isoform C (Cdc25C) degradation via ubiquitin-proteasome pathways. Mutation of the putative KEN box within the region 151 to 157 of human Cdc25C or treatment of the cells with a peptide competitor encompassing the KEN box partially inhibited arsenite-induced ubiquitination of Cdc25C. Thus, these results indicate that the regulated ubiquitination of Cdc25C may be involved in the arsenite-induced proteolytic down-regulation of Cdc25C activity in the G2/M phase of the cell cycle and suggest a link between cell cycle and the carcinogenic effects of arsenite.

Carcinogens; Humans; Tumorigenesis; Genotoxic-effects; Arsenites; Peptides; Proteins; Occupational-exposure; Environmental-exposure; Arsenic-compounds; Dermatosis; Cardiovascular-system-disorders; Lung-cancer; Bladder-cancer; Liver-cancer; Kidney-disorders; Skin-cancer

Health Effects Laboratory Division, National Institute for Occupational Safety and Health, 1095 Willowdale Road, Morgantown, WV 26505

7440-38-2

20020219

Journal Article

lfd3@cdc.gov

Kirschner-MW

2002

4

1091-6490

HELD

Proceedings of the National Academy of Sciences of the United States of America

WV; MO