Impact of preirradiation of the tumour bed on cell production rate and cell loss of human FaDu squamous cell carcinoma growing in nude mice

Citation
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
Citations number
26
Categorie Soggetti
Experimental Biology
Journal title
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
ISSN journal
09553002 → ACNP
Volume
75
Issue
10
Year of publication
1999
Pages
1293 - 1297
Database
ISI
SICI code
0955-3002(199910)75:10<1293:IOPOTT>2.0.ZU;2-J
Abstract
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.