Aberrant crypt foci (ACF) are present in carcinogen treated rodent col
ons and in the colons of humans with a high risk for developing the di
sease. It is proposed that ACF are preneoplastic lesions. Quantificati
on of the number and growth features of ACF has been employed to study
modulators of colon carcinogenesis. In this review, examples are pres
ented to support the concept that ACF are preneoplastic lesions and th
at sequential quantification of their number and growth features (cryp
t multiplicity) in animal colons may provide further insight into the
pathogenesis of colon cancer. It is proposed that cellular and molecul
ar heterogeneity among ACF with different growth and morphologic featu
res will be invaluable in the identification of events critically asso
ciated with cancer development.