The maintenance of a constant number of cells in an adult organism is a tig
htly regulated process. This is particularly important in organs where cell
s are in a constant rate of renewal during the entire lifespan. In these or
gans, cell number homeostasis is the direct consequence of a bal-ance betwe
en cell proliferation and apoptosis. The colonic epithelium is an example o
f such a site and the high prevalence of colon cancer makes the understandi
ng of cell number homeostasis more important to define. Normal colonic epit
helium is organized in crypts where cell proliferation, migration, differen
tiation and apoptosis are topographically organized in a linear fashion alo
ng the crypt axis. Normal colonic crypts are composed of stem cells at the
base, a proliferation and a differentiation zone in the lower third of the
crypt, a migration zone in the upper two-thirds, and the surface epithelium
where senescent cells are eliminated by apoptosis. Globally, apoptosis can
be defined as a normal process of cell suicide, critical for development a
nd tissue homeostasis. Colonic epithelial cells migrate from the base of th
e crypt to the surface epithelium in 6-7 days. The normal architecture of t
he crypt is maintained by a balance between cell proliferation at the base
and apoptosis at the top of the crypt and surface epithelium.