The radiologist has the opportunity to be involved at every level of the ge
ne therapy effort: characterizing the disease, choosing sites for gene ther
apy, contributing to gene delivery, monitoring uptake in tissues of interes
t, measuring levers of target gene expression, and evaluating clinical resp
onse. Development of practical and efficient methods to introduce genetic m
aterial into target cells is a prerequisite to its successful use in oncolo
gy. Ultrasound, computed tomography (CT) and magnetic resonance imaging (MR
I) provide guidance far biopsies and intratumoral injections in the course
of the therapy Besides percutaneous application, delivery via organ-specifi
c vascular supply and other anatomically preformed routes are being evaluat
ed. Catheters, balloons and stents will be adopted as carrier devices from
vascular to oncologic gene therapy. Control of gene transcription by ionizi
ng radiation in vivo represents another novel method of spatial and tempora
l regulation of gene-based cancer treatment. Because of the risks involved
in delivery, confirmation of the effect at the genome or phenotypic level i
s highly appreciated. Radiologic monitoring during gene delivery offers an
opportunity to limit the effect of inadequate targeting. The demand for ima
ging gene expression in vivo by probing the molecular substrates that readi
ly bind to imaging labels such as radioactive or paramagnetic metal ions is
evident. Gene transfer can be visualized with scintigraphy and MRI in cell
culture as well as in vivo. There is a potential usefulness of MRI in dire
ctly monitoring expression of gene products with paramagnetic properties su
ch as melanin.