Carcinogenesis, Vol 19, 889-896, Copyright © 1998 by Oxford University Press
SC Huang and TC Lee
Arsenical compounds, known to be human carcinogens, were shown to disturb
cell cycle progression and induce cytogenetic alterations in a variety of
cell systems. We report here that a 24 h treatment of arsenite induced
mitotic accumulation in human cell lines. HeLa S3 and KB cells were most
susceptible: 35% of the total cell population was arrested at the mitotic
stage after treatment with 5 microM sodium arsenite in HeLa S3 cells and
after 10 microM in KB cells. Under a microscope, we observed abnormal
mitotic figures in arsenite-arrested mitotic cells, including deranged
chromosome congression, elongated polar distance of mitotic spindle, and
enhanced microtubule immunofluorescence. The spindle microtubules of
arsenite-arrested mitotic cells were more resistant to nocodazole-induced
dissolution than those of control mitotic cells. According to turbidity
assay, arsenite at concentrations below 100 microM significantly enhanced
polymerization of tubulins. Since spindle dynamics play a crucial role in
mitotic progression, our results suggest that arsenite-induced mitotic
arrest may be due to arsenite's effects on attenuation of spindle dynamics.
ARTICLES
Arsenite inhibits mitotic division and perturbs spindle dynamics in HeLa S3 cells
Institute of Biomedical Sciences, Academia Sinica, National Defense Medical Center, Taipei, Taiwan, ROC.
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