Kk. Bose et al., DIFFERENTIAL-EFFECTS OF NITROGEN-MUSTARD IN-VIVO ON THE CANCER AND HOST-CELLS IN MCA-11 TUMORS, Cell proliferation, 28(7), 1995, pp. 403-414
We analysed the effects of nitrogen mustard (HN2) on the growth, cell
cycle distributions, and ratios of tumour cells to host cells for MCa-
11 tumours grown in vivo. Treatment of tumour-bearing BALB/c mice with
3 mg/kg of HN2 produced a significant slowing of MCa-11 tumour growth
. Seventy-two hours after treatment in vivo with either 3 or 4 mg/kg o
f HN2, the host cells in the treated tumours showed a significantly de
creased G(0)/G(1) peak and an increased G(2)/M peak (P < 0.01), wherea
s the cancer cells in the treated tumours showed significant increases
in the G(0)/G(1) peak coupled with relatively decreased proportions o
f S and G(2)/M tumour cells (P < 0.001). The ratio of the total number
of cancer cells to the total number of host cells in the tumours was
significantly increased 72 h after HN2 administration (P < 0.01), Thir
ty-two days after treatment with HN2, the cell cycle distributions of
the host and tumour cells in the treatment and control tumours had ret
urned to being identical, but the ratio of the total number of cancer
cells to the total number of host cells remained increased in the trea
ted tumours (P < 0.01). These results show that the administration in
vivo of HN2 can lead to entirely different cell cycle effects for the
host and cancer cells in the same tumour, and that the partial growth
arrest of MCa-11 tumours from HN2 treatment may be due in part to the
preferential destruction of host cells rather than solely to a direct
cytotoxic effect on the cancer cells.