I. Ding et al., RADIOPROTECTION OF HEMATOPOIETIC-TISSUE BY FIBROBLAST GROWTH-FACTORS IN FRACTIONATED RADIATION EXPERIMENTS, Acta oncologica, 36(3), 1997, pp. 337-340
Acidic and basic fibroblast growth factors (FGF(1/2)) myeloprotect mic
e in single dose total body irradiation (TBI) experiments with a dose
modification factor (DMF) of approximate to 1.15. CFU-C assay suggests
that one of the mechanisms is augmentation of the shoulder of the rad
iation dose response curve, and thus protection could be greater with
fractionation. Four equal fractions of TBI were delivered to C3H/He mi
ce at times 0 h, 8 h, 24 h, and 32 h. FGF(1/2) dose was 3 mu g per iv
injection given 24 and 4 hrs before the first radiation dose. FGF(2) t
reated mice had a significant survival advantage over saline-treated m
ice with a DMF of 1.22 +/- 0.07 (p < 0.01). Adding a third dose of FGF
(2), had no additional benefit on LD50/30 (dose of radiation lethal to
50% of animals measured at day 30) (DMF = 1.23 +/- 0.06, p < 0.01). F
GF(1) was not as effective with fractionation (DMF = 1.04 +/- 0.03). I
ncreased survival in FGF2 treated mice was due to the a more rapid rec
overy of bone marrow hematopoietic cells and peripheral WBC, RBC and p
latelets. FGF(2) may prove a useful treatment response modifier in cli
nical fractionated irradiation.