Abstract |
KIN-806 is one of the 2-nitroimidazole derivative hypoxic cell radiosensitizers. Its radiosensitizing effects and the degree of lung metastasis detected were evaluated and compared with its analogs KIN-804 and KIN-844. The immune reactions induced by these radiosensitizers were also analyzed. Female C3H/He mice and SCCVII tumor cells were used. Seventeen days after inoculation of SCCVII tumor cells into the animals, 0.4 g/kg of KIN-806, KIN-804, and KIN-844 was administered to each radiosensitizer group 30 min before 40 Gy was delivered as local irradiation. In each group, KIN-806, KIN-804, and KIN-844 markedly suppressed tumor regrowth in comparison with animals that received irradiation alone. There was no significant difference in the radiosensitizing effects among these three radiosensitizers. A marked suppression of lung metastasis and macrophage/T-lymphocyte infiltration into the tumor were observed only in the KIN-806-administered groups, regardless of the presence or absence of radiation therapy. It therefore appears likely that the lung metastasis suppression was caused by the immune reaction elicited by KIN-806, which is an excellent immunopotentiator as well as an effective radiosensitizer.
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Authors | T Inomata, Y Ogawa, A Nishioka, N Hamada, S Ito, S Kariya, S Yoshida, H Nagasawa, H Hori, S Inayama |
Journal | Oncology reports
(Oncol Rep)
1999 Nov-Dec
Vol. 6
Issue 6
Pg. 1209-12
ISSN: 1021-335X [Print] Greece |
PMID | 10523682
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Hydroxamic Acids
- KIN 806
- Nitroimidazoles
- Radiation-Sensitizing Agents
- 2-nitroimidazole-1-methylacetohydroxamate
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Topics |
- Animals
- Cytotoxicity, Immunologic
- Female
- Hydroxamic Acids
(administration & dosage)
- Lung Neoplasms
(drug therapy, immunology, radiotherapy, secondary)
- Mice
- Mice, Inbred C3H
- Neoplasms, Experimental
(drug therapy, immunology, pathology, radiotherapy)
- Nitroimidazoles
(administration & dosage)
- Radiation-Sensitizing Agents
(administration & dosage)
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