Antimelanoma effects of
4-S-cysteaminylphenol (4-S-CAP), which is a newly synthesized
melanin precursor, as a chemotherapeutic agent specific to
malignant melanoma were determined in an in vivo system using mouse
B16 melanoma. The
intraperitoneal injection of 4-S-CAP induced a slight delay in the growth period of subcutaneous
melanoma of C57BL/6 mice. Survival times of mice
after treatment with 4-S-CAP were a little longer than those of control mice (P < 0.05), although all mice died from the local growth of tumours. The viable cell ratio of in vivo subcutaneous tumour cells reduced to 52.8% within 24 h
after treatment with 4-S-CAP, but the ratio had recovered to the control level 72 h
after treatment (> 90%). Similarly, the
proliferating-cell-nuclear-antigen-positive cell ratio of melanotic
melanoma had reduced 24 h
after treatment and recovered within 72 h
after treatment, while 4-S-CAP had no effect on amelanotic tumours. The formation of lung colonies by intravenous inoculation of
malignant melanoma cells was compared between mice with
intraperitoneal injection of 4-S-CAP and
phosphate-buffered saline only. The 4-S-CAP-treated mice had significantly fewer lung colonies compared with the control mice (P < 0.01). The results indicate that the agent, 4-S-CAP, would have a
therapeutic effect on
malignant melanoma for a short time in vivo and therefore the agent can be effective against a small number of tumour cells, such as lung colonies, although it had little effect on the local tumours.