The protein kinase C (PKC) family of serine/ threonine kinases consists of
at least 11 mammalian isoforms, which show slight differences in their mole
cular structure and enzymatic properties. PKC isoforms are involved in a wi
de variety of intracellular signalling events and play an important role in
tumour promotion and cell growth control in general. Studies of expression
levels in cancer cells and studies using overexpression of single isoforms
or expression of dominant negative isoforms reveal that, depending on the
cellular background, PKC isoforms can either promote or inhibit cell growth
. To understand the role of PKC isoforms in growth control, it is essential
to understand how PKC functions in the intracellular signalling cascades t
owards the cell nucleus. Recent work has shown that PKC isoforms can act ei
ther in the cytoplasm, and cause nuclear effects indirectly by triggering s
ignalling pathways directed towards the cell nucleus, or, after translocati
on and activation, can themselves act in the cell nucleus.