There have been tremendous advances in our understanding of cancer fro
m the application of molecular biology over the past decade. The disea
se is caused by a series of defects in the genes that accelerate growt
h-oncogenes-and those that slow down cellular turnover-tumour suppress
or genes. The proteins they encode provide a promising hunting ground
in which to design and test new anticancer drugs. Several treatment st
rategies are now under clinical trial entailing direct gene transfer.
These include the use of gene marking to detect minimal residual disea
se, the production of novel cancer vaccines by the insertion of genes
which uncloak cancer cells so making them visible to the host's immune
system, the isolation and coupling of cancer specific molecular switc
hes upstream of drug activating genes, and the correction of aberrant
oncogenes or tumour suppressor genes. The issues in these approaches a
re likely to have a profound impact on the management of cancer patien
ts as we enter the next century.