Considerable progress has been made over the past year in elucidating
the mechanisms by which extracellular signals are transduced via cell
surface receptors to trigger changes in gene expression which determin
e the growth and differentiated state of a cell. In particular, Ras pr
oteins have been implicated as key intermediates that mediate the sign
al from upstream tyrosine kinases to a downstream cascade of serine/th
reonine kinases, which then activate nuclear factors that control gene
expression and protein synthesis. How Ras proteins function is regula
ted in this role as a molecular switch, and how the signal is transmit
ted between the various components of the pathway, are now being deter
mined. Finally, the Rho family of Ras-related proteins, which regulate
the actin cytoskeleton, have also been implicated as mediators of onc
ogenic Ras transformation. The brisk pace at which the key components
of Ras-mediated signal transduction pathways are being identified hold
great promise that new targets for therapeutic intervention in cancer
may now be identified.