C. Petersen et al., Impact of preirradiation of the tumour bed on cell production rate and cell loss of human FaDu squamous cell carcinoma growing in nude mice, INT J RAD B, 75(10), 1999, pp. 1293-1297
Purpose: To explore whether the tumour bed effect (TBE) in FaDu squamous ce
ll carcinoma growing in nude mice is caused by a reduced tumour cell produc
tion rate and/or by increased tumour cell loss.
Materials and methods: Human FaDu tumours were studied in NMRI nude mice. T
he volume doubling time (VDT) between 100 and 400 mm(3) was determined for
tumours in unirradiated subcutaneous (sc) tissues (group 1), tumours in sc
tissues preirradiated with 12.5 Gy (group 2), tumours irradiated in situ wi
th 12.5 Gy (group 3), and tumours from group 3 re-transplanted into unirrad
iated sc tissues (group dr). Labelling index (LI), potential doubling time
(T-pot), relative necrotic area and apoptotic index (AI) were evaluated in
tumours from groups 1 and 2.
Results: The median VDT were 2.6 days (95% CI 2-4) in group 1 and 7.0 days
(4-15) in group 2 (P<0.001). The VDT were not significantly different betwe
en groups 2 and 3, and group 1 and 4. In groups 1 and 2, the T-pot values (
3.1 +/- 0.6 days (SD) versus 2.9+/-0.5 days) and the LI were identical (10/-1.5%). The median relative necrotic area was significantly larger in grou
p 2 (37% [23-42]) compared with group (6% [0.3-27]). The apoptotic index wa
s low (0.2%) and did not differ between groups 1 and 2.
Conclusions: The results indicate that the TEE in FaDu squamous cell carcin
oma is not caused by a reduced cell production rate in the viable tumour co
mpartment. Rather, the TEE reflects a decreased viable tumour cell compartm
ent due to increased cell loss. Necrosis appears to be the major component
of the tumour bed induced cell loss in FaDu tumours, whereas apoptosis has
no impact on the TEE in this model.