Initially described as a unique entity, protein kinase C (PKC) is now
represented by a family of 11 isoforms which differ in their structura
l and biochemical properties as well as in their tissular distribution
subcellular localization and substrate specificity. So far a lot of s
tudies have attempted to approach the role of each of these PKC isofor
ms in the deregulation of growth signaling that leads to carcinogenesi
s. Among the various strategies developed, the surexpression of specif
ic isoforms in different cellular models is the strategy which led to
major advances as concern the PKC-cancer relationship. This review rep
orts the main results obtained in this field especially in that of col
orectal cancer.