Tumors grafted into mice may modify the proliferation of normal cell p
opulations. In this paper, we have studied the evolution of mitotic ac
tivity (MA) in duodenal-crypt enterocytes of ES12a hepatocarcinoma-bea
ring mice; a total of 87 28-day-old female animals of the C3H/S strain
were used after standardization for circadian-periodicity analysis. T
he mice were distributed into two groups: those remaining intact and t
hose receiving tumor grafts. Each group was then divided into six batc
hes (n = 6-10), one of which was sacrificed every 4 h over a period of
one day. A dose of colchicine (2 mu g/g) was administered to each ani
mal 4 h before killing. Samples of duodenum were fixed in 10% (v/v) bu
ffered formalin and processed for assessment of mitotic activity. The
number and topographic localization of the colchicine-arrested metapha
ses were recorded among the entero-cytes within 20 longitudinal sectio
ns of the duodenal crypts in each animal. From these data the mitotic
indices over the total crypt-cell population as well as within each pr
eviously-established zone were determined along with (x) over bar +/-
SEM for each experimental group. The statistical significance of the d
ifferences among the data were analyzed by Student t test. The results
show that the presence of ES12a tumor inhibits the mitotic activity o
f the duodenal-crypt enterocytes and produces an apparent temporal shi
ft in the peak and trough within the circadian curve for this growth p
arameter.