Different G{sub 2}/M accumulation in M059J and M059K cells after exposure to DNA double-strand break-inducing agents
Journal Article
·
· International Journal of Radiation Oncology, Biology and Physics
- Department of Oncology-Pathology, Unit of Medical Radiation Biology, Karolinska Institutet, Stockholm (Sweden)
- Research Group of Tumour Genetics and Molecular Cytogenetics, Institute of Medical Genetics, Charite, Humbolt University of Berlin, Berlin (Germany)
- Cellular and Molecular Analysis, Karolinska Institutet, Stockholm (Sweden)
- Division of Medical Radiation Physics, Karolinska Institutet, Stockholm (Sweden)
Purpose: To investigate and compare the cell cycle progression in relation to cell death in the human glioma cell lines, M059J and M059K, after exposure to DNA double-strand break-inducing agents. Methods and materials: The M059J and M059K cells, deficient and proficient in the catalytic subunit of the DNA-dependent protein kinase, respectively, were exposed to 1 and 4 Gy of photons or accelerated nitrogen ions. In addition, M059J and M059K cells were treated with 10 and 40 {mu}g/mL of bleomycin for 30 min, respectively. Cell cycle progression, monitored by DNA flow cytometry, was measured up to 72 h after treatment. Results: M059J, but not M059K, cells displayed G{sub 2}/M accumulation after low linear energy transfer irradiation. High linear energy transfer radiation exposure however, resulted in a substantial increase of M059K cells in the G{sub 2}/M phase detected at 48 h. At 72 h, the number of cells in the G{sub 2}/M phase was equivalent to its control. M059J cells accumulated mainly in S phase after high linear energy transfer irradiation. In contrast to M059K, M059J cells were still blocked at 72 h. Bleomycin induced G{sub 2}/M accumulation for both M059J and M059K cells detected 24 h after treatment. At 48 h, the percentage of bleomycin-treated M059J cells in G{sub 2}/M phase remained high, and the number of M059K cells had decreased to control levels. Neither cell line showed cell cycle arrest ({<=}10 h) after exposure to these agents. Conclusion: Distinct cell cycle block and release is dependent on the complexity of the induced DNA damage and the presence of the DNA-dependent protein kinase catalytic subunit.
- OSTI ID:
- 20633105
- Journal Information:
- International Journal of Radiation Oncology, Biology and Physics, Journal Name: International Journal of Radiation Oncology, Biology and Physics Journal Issue: 3 Vol. 61; ISSN IOBPD3; ISSN 0360-3016
- Country of Publication:
- United States
- Language:
- English
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