Lack of interferon beta-induced radiosensitization in four out of five human glioblastoma cell lines.

PURPOSE: To investigate the potential of interferon beta to enhance the cytotoxic activity of ionizing irradiation against glioma cells, and to elucidate the possible mechanisms responsible for conflicting clinical results. METHODS AND MATERIALS: Five glioblastoma cell lines (U87MG, U118MG, U373MG, MO59K, MO59J) with different radiosensitivity and genetic background were used. Experiments were performed in exponentially growing cultures, and cell survival was measured by a colony-forming assay. Cells were incubated with natural interferon beta (n-IFN-beta; 30-3000 IU/mL) for 24 h followed by single dose irradiation with 1 to 6 Gy of gamma-rays. RESULTS: Significant differences in n-IFN-beta sensitivity were found. The cell lines also differed in their radiation sensitivity, and there was no correlation between the n-IFN-beta and the radiation sensitivity. In three of five cell lines, the interaction of n-IFN-beta and irradiation was infra-additive; in one cell line, it was additive. For MO59J cells only, which are NHEJ-deficient, supra-additivity was observed. CONCLUSION: Our results confirm the remarkable heterogeneity that is characteristic of malignant glioma. The combined effect of n-IFN-beta and radiation was mostly infra-additive or additive; synergistic interaction might occur in tumor cells that already have acquired repair deficiencies because of their genetic instability, as shown for the MO59J cell line.

Combined effect of topotecan and irradiation on the survival and the induction of chromosome aberrations in vitro.

BACKGROUND: Topotecan demonstrated radiosensitizing effects in vivo and in vitro, which are schedule- and cell line dependent. The underlying mechanisms are not fully understood. Topotecan interferes with DNA replication, transcription, and repair and may thus increase the frequency of radiation-induced lethal chromosome aberrations. MATERIAL AND METHODS: U-373 MG glioblastoma cells, WiDr colon adeno-carcinoma cells, as well as normal human fibroblasts and lymphocytes were irradiated (0-6 Gy) and exposed to varying topotecan doses (0.01-10 microM) always 15 minutes before and either 1 hour after (short-term) or 24 hours after (long-term) irradiation. Survival was measured by colony-forming assays, and chromosome aberrations were scored in Giemsa-stained metaphase spreads. Unirradiated cells served as specific controls. RESULTS: Topotecan alone reduced the clonogenic cell survival in a concentration- and time-dependent manner, and radiosensitization was observed for all cell lines tested. There was no correlation between clonogenic cell survival and the frequencies of treatment-induced chromosomal aberrations, neither in tumor cells nor in fibroblasts. In contrast, in lymphocytes increased frequencies of radiation-induced dicentric chromosomes were seen after the combined treatment. CONCLUSION: In certain cell types combined radiation/topotecan treatment may lead to increased frequencies of lethal chromosome aberrations. However, there is no evidence that the increased formation of lethal chromosome aberrations plays an important role in the topotecan-induced radiosensitization of human tumors.