Preventive effect of matrix metalloproteinase inhibitor, R-94138, in combination with mitomycin C or cisplatin on peritoneal dissemination of human gastric cancer cell line TMK-1 in nude mice

Citation
N. Igarashi et al., Preventive effect of matrix metalloproteinase inhibitor, R-94138, in combination with mitomycin C or cisplatin on peritoneal dissemination of human gastric cancer cell line TMK-1 in nude mice, JPN J CANC, 90(1), 1999, pp. 116-121
Citations number
24
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
JAPANESE JOURNAL OF CANCER RESEARCH
ISSN journal
09105050 → ACNP
Volume
90
Issue
1
Year of publication
1999
Pages
116 - 121
Database
ISI
SICI code
0910-5050(199901)90:1<116:PEOMMI>2.0.ZU;2-2
Abstract
R-94138, a matrix metalloproteinase inhibitor, was examined for the ability to prevent peritoneal dissemination of a human gastric cancer xenograft, T MK-1. When the supernatant of a co-culture of TMK-1 cells and human normal fibroblast cells was subjected to gelatin zymography, it was clear that the protein expression of MMP-2 had been inhibited by R-94138. When TMK-1 was injected intraperitoneally (i.p.) into nude mice at 5 x 10(5) cells/body, t he resulting peritoneal dissemination mimicked clinical carcinomatous perit onitis. When the maximum tolerated dose of mitomycin C (MMC) or cisplatin ( DDP) was given 12 h after the tumor inoculation, peritoneal dissemination w as completely inhibited, while the effect of R-94138 was limited when it wa s given i.p. at a dose of 20 mg/kg in a schedule of q.d. x5 starting 12 h a fter tumor injection. MMC and DDP also suppressed peritoneal dissemination when they were administered 1 week after the tumor inoculation at a single dose of 2 and 3 mg/kg i.p., respectively. R-94138 inhibited peritoneal diss emination when it was administered i.p. at a dose of 30 mg/kg in a schedule of q.d. x5 starting from 1 week after tumor injection. The combination of MMC and R-94138 increased the preventive effect on peritoneal dissemination . R-94138 seems to be a promising candidate to prevent peritoneal dissemina tion of gastric cancer.