Tumour development is a disease of both somatic and genetic origin. It
originates from a combination of oncogene and tumour suppressor alter
ations that force the cell into unprogrammed proliferation. It is reas
onable to think that a genetic disease could be cured by gene therapy,
and several strategies along this line are presently being employed.
The use of retroviruses to carry 'suicide' genes has been the most suc
cessful approach to date for the treatment of neurological malignancie
s. The use of adenoviruses with deletions in the E1B region opens a ne
w and elegant possibility for the destruction of tumours deficient in
the p53 suppressor gene. Strategies based on the inhibition of angioge
nesis are being developed, and those based on blockade of inducers of
angiogenesis have given encouraging results in experimental animal mod
els. However, gene therapy has not yet been able to permanently cure a
human genetic disease, thereby creating a certain degree of caution a
mong scientists and clinicians.