The objective of this study was to develop a brain tumor model in a mouse w
here gene therapy could be delivered either directly into a pre-established
tumor bed or prophylacticly prior to tumor delivery (protective treatment)
. Micro-cannulas were constructed from metal tubing, implanted into the rig
ht frontal lobe of mice, and then secured in place in the skull with cement
. Experiments evaluating the usefulness, reproducibility and morbidity of t
he system were performed. It was found that tumor cells could reproducibly
be delivered into the right frontal lobe of the mice. Two tumors could be p
recisely delivered into the same area following injections at different tim
es. Repeat injections were performed without a stereotaxic frame and withou
t the need for repeat intracerebral needle tracts. There were no noticeable
side effects of maintaining the cannulas in place for long periods of time
. In summary, this system is useful for studying the effects of various tre
atment strategies on established brain tumors in a mouse model which more c
losely simulates the clinical situation. It obviates the need for time cons
uming stereotaxic procedures or repeat invasive intracerebral injections.