Gene therapy is a newly hatched field of biomedical research aimed at
introducing therapeutically important genes into somatic cells of pati
ents for the treatment of human disease. Whereas for inborn errors of
metabolism transfer of a single gene can correct the disorder, cancer
is a complex disease involving mutations in a number of protooncogenes
and tumor suppressor genes as well as an imbalance and disarray in ph
osphorylation events and regulatory circuits of the cell cycle; transf
er of the wild-type p53 or p21 tumor suppressor genes is a successful
gene therapy approach leading to apoptotic death of cancer cells or in
restrain of their chaotic growth. A different promising approach is t
ransfer of the herpes simplex virus thymidine kinase (HSV-tk) gene (su
icide gene) and systemic treatment with the prodrug ganciclovir which
is converted by HSV-tk into a toxic drug killing dividing cells. Expre
ssion of suicide genes, p53, and other therapeutic genes preferentiall
y in cancer cells can be achieved by regulatory elements from tumor-sp
ecific genes such as carcinoembryonic antigen, BRCA1, and PSA.