Saito Y, Mitsuhashi N, Takahashi T, Sakurai H, Nozaki M, Ishikawa H, Nasu S, Hayakawa K, Niibe H
Department of Radiology and Radiation Oncology, Gunma University School of Medicine, Maebashi, Japan.
Int J Radiat Biol. 1998 Feb;73(2):225-31. doi: 10.1080/095530098142626.
To investigate the differences between two rat yolk sac tumour cell lines with different radiosensitivities in paclitaxel sensitivity and in the sensitizing effects of paclitaxel in combination with irradiation.
NMT-1 is a parent radiosensitive cell line and NMT-1R is a variant radioresistant cell line.
Clonogenic assay demonstrated almost the same paclitaxel sensitivity with Do of 5.15 nM in NMT-1 and 5.02 nM in NMT-1R. Many apoptotic cells and DNA ladder formations were observed at 24 h after exposure to paclitaxel in both cell lines. The incidence of DNA fragmentation after 24 h exposure to 20 nM paclitaxel was 12.4 +/- 3.3% for NMT-1, and 13.0 +/- 1.9% for NMT-1R. Paclitaxel showed a supra-additive effect in combination with irradiation in both cell lines at 12 h after paclitaxel treatment only when the accumulation of cells in the G2/M phase reached its peak.
Paclitaxel had the same cytotoxic effect in two cell lines with different radiosensitivity due to the induction of apoptosis. A supra-additive effect to radiation was observed with 12 h pretreatment in both cell lines. Paclitaxel may be effective for tumours with a component of different radiosensitivity in combination with irradiation.