Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

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
 [1];  [2];  [3];  [4];  [1];  [4]
  1. Department of Oncology-Pathology, Unit of Medical Radiation Biology, Karolinska Institutet, Stockholm (Sweden)
  2. Research Group of Tumour Genetics and Molecular Cytogenetics, Institute of Medical Genetics, Charite, Humbolt University of Berlin, Berlin (Germany)
  3. Cellular and Molecular Analysis, Karolinska Institutet, Stockholm (Sweden)
  4. 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

Similar Records

Radiation-induced DNA damage and repair in cells of a radiosensitive human malignant glioma cell line
Journal Article · Thu Nov 30 23:00:00 EST 1995 · Radiation Research · OSTI ID:186111

Modulation of radiation-induced apoptosis and G{sub 2}/M block in murine T-lymphoma cells
Journal Article · Tue Feb 28 23:00:00 EST 1995 · Radiation Research · OSTI ID:81190

Transient failure to dephosphorylate the cdc2-cyclin B1 complex accompanies radiation-induced G{sub 2}-phase arrest in HeLa cells
Journal Article · Fri Sep 01 00:00:00 EDT 1995 · Radiation Research · OSTI ID:146886