We examined the ability of sulfonylurea derivative, DW2143 (4-phenyl-1-[1-(4-aminobenzoyl)-
indoline-5-sulfonyl]-4,5-dihydro-2-imida
zolone hydrochloride), to inhibit the growth of
tumor cells in vitro and in vivo. When its anti-proliferative activities were tested on five murine
tumor (B 16, Colon26, E1-4, 3LL and P388) and nine human
tumor (BxPC-3, HepG2, Lovo, MCF-7, NCI-H69, SW480, WiDR, KB and KBV20C) cells of diverse tissue origins, the in vitro antitumor activities of DW2143 were comparable to those of
doxorubicin against all tumor cell lines. In addition, the anti-proliferative activities of DW2143 against KBV20C, a
vincristine-resistant cell line, are similar or superior to those of
doxorubicin. When the in vivo antitumor activities using three murine
tumor cells were tested after
oral administration of DW2143, a wide range of
tumor growth inhibition was observed.
Tumor growth inhibition against 3LL at doses of 50 and 100 mg/kg DW2143 was 84.3% and 47.2%, respectively, which was comparable or superior to those of
doxorubicin (5 mg/kg).
Tumor growth inhibition of B16 at a dose of 100 mg/kg in the DW2143-treated group was 42% as compared to 54% for
doxorubicin (5 mg/kg). When mice implanted with Colon26 were tested,
tumor growth inhibition at a dose of 80 mg/kg DW2143 was 36% as compared with 37% for
doxorubicin (5 mg/kg). Taken together, these results indicate that the novel sulfonylurea derivative, DW2143, is an attractive candidate for further development as a useful oral anticancer
drug.