Repopulation characteristics and cell kinetic parameters resulting from multi-fraction irradiation of xenograft tumors in SCID mice

Citation
E. Sham et Re. Durand, Repopulation characteristics and cell kinetic parameters resulting from multi-fraction irradiation of xenograft tumors in SCID mice, INT J RAD O, 43(3), 1999, pp. 617-622
Citations number
19
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
ISSN journal
03603016 → ACNP
Volume
43
Issue
3
Year of publication
1999
Pages
617 - 622
Database
ISI
SICI code
0360-3016(19990201)43:3<617:RCACKP>2.0.ZU;2-H
Abstract
Purpose: Cell kinetics and repopulation rates during multifraction irradiat ion have previously been measured in SiHa human cervical carcinoma cells gr own as spheroids. The current study applied similar techniques to SiHa tumo r xenografts with the ultimate goal of assessing the clinical prognostic va lue of in situ cell kinetics. Methods and Materials: SiHa (human squamous cell cervical tumor) cells were inoculated subcutaneously in the flank or back of SCID mice. When tumors r eached a size of 200-300 mg, they received 25 Gy in 10 fractions over 5 day s. Tumor regrowth and cell kinetics parameters were followed during treatme nt, and for 10 days after completion by measuring tumor volume and analyzin g cellular BrdUrd and IdUrd incorporation with how cytometry, Results: Tumor volume was of limited use in assessing response to irradiati on, The fraction of proliferating cells increased early during irradiation as did the labeling index; potential doubling time (T-pot) decreased during treatment and returned to the pre irradiation value after treatment. Cell cycle time remained relatively constant throughout the experiments. Conclusion: These results confirm the feasibility of evaluating cell cycle kinetics and repopulation parameters in a murine tumor model undergoing a f ractionated course of irradiation. Repopulation of clonogenic tumor cells o ccurred more rapidly than predicted by pretreatment measurements, primarily due to an increased growth fraction and consequent decrease in T-pot. (C) 1999 Elsevier Science Inc.