Split-dose and Low Dose-rate Recovery in Four Experimental Tumour Systems
- 1 January 1987
- journal article
- research article
- Published by Taylor & Francis in International Journal of Radiation Biology and Related Studies in Physics, Chemistry and Medicine
- Vol. 52 (1) , 157-170
- https://doi.org/10.1080/09553008714551581
Abstract
The radiation dose-rate effect has been investigated in three murine tumour cell systems (MT carcinoma, Lewis lung tumour, B16 melanoma) and in the HX34 human melanoma xenograft taken directly from mice and irradiated in vitro. The four tumour types were remarkably similar in their radiation response characteristics, especially at low dose rate, the Lewis lung tumour tended to be the most radiosensitive at high dose rate. The data have been analysed using the Lethal-Potentially Lethal (LPL) model of Curtis and the Incomplete Repair (IR) model of Thames. The data are equally well fitted by both models. The most remarkable feature of these analyses is that both models lead to estimates for the half-time for recovery that are in the region of 0.1 h, considerably shorter than other published values. Split-dose experiments were also performed, taking care to keep the cells at 37.degree. C between exposures. In all cases the split-does half times were longer than the values derived from dose-rate analysis and in the case of the Lewis lung and HX34 tumour lines the difference was by almost a factor of ten. The discrepancy between these estimates could be the result of biphasic cellular recovery.This publication has 12 references indexed in Scilit:
- Dose-rate effects and the repair of radiation damageRadiotherapy and Oncology, 1986
- An ‘Incomplete-repair’ Model for Survival after Fractionated and Continuous IrradiationsInternational Journal of Radiation Biology, 1985
- EFFECTS OF THE NUCLEOSIDE ANALOGS ALPHA-ARA-A, BETA-ARA-A AND BETA-ARA-C ON CELL-GROWTH AND REPAIR OF BOTH POTENTIALLY LETHAL DAMAGE AND DNA DOUBLE STRAND BREAKS IN MAMMALIAN-CELLS IN CULTURE1983
- Enhancement of cytotoxic drugs by misonidazole (MISO) in Lewis lung tumors of different sizes, and mouse bone marrowInternational Journal of Radiation Oncology*Biology*Physics, 1982
- Repopulation of γ-irradiated Lewis lung carcinoma by malignant cells and host macrophage progenitorsBritish Journal of Cancer, 1978
- Enhancement by cytotoxic agents of artificial pulmonary metastasisBritish Journal of Cancer, 1977
- A soft agar colony assay for Lewis lung tumour and B16 melanoma taken directly from the mouseBritish Journal of Cancer, 1976
- A molecular theory of cell survivalPhysics in Medicine & Biology, 1973