Abstract
The effect of misonidazole (MISO), local hyperthermia (HT) and their combination on radiation-induced chromosome damage and micronucleus (MN) induction was studied in mouse bone marrow cells. It was found that MISO treatment did not enhance the clastogenic effect of radiation, which indicates a lack of radiosensitization of bone marrow chromosomes. But post-irradiation HT increased the frequency of aberrant cells and MN. A combination of MISO and HT produced a significant increase in the frequency of radiation-induced aberrant cells and MN at all the radiation doses as compared to radiation alone. The percentage of aberrant cells as well as the percentage of MN showed a linear quadratic increase with radiation dose in all the treatment groups. At higher radiation doses, cells with < 1 MN increased quadratically with a pronounced increase in cells bearing < 2 MN and severely damaged cells (SDCs) at radiation doses above 3.0 Gy in the HT and MISO + HT traeated groups. Our results indicate that though MISO itself may not have a radiosensitizing effect on mouse chromosomes, a combination of MISO with HT can enhance the radiation damage in normal bone marrow.
Original language | English |
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Pages (from-to) | 913-918 |
Number of pages | 6 |
Journal | Acta Oncologica |
Volume | 34 |
Issue number | 7 |
DOIs | |
Publication status | Published - 01-01-1995 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Oncology
- Radiology Nuclear Medicine and imaging
- Hematology