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基质金属蛋白酶抑制剂R-94138联合丝裂霉素C或顺铂对人胃癌细胞系TMK-1在裸鼠腹腔内播散的预防作用

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.

作者信息

Igarashi N, Kubota T, Otani Y, Matsuzaki S W, Watanabe M, Teramoto T, Kumai K, Tamaki K, Tanzawa K, Kobayashi T, Kitajima M

机构信息

Department of Surgery, School of Medicine, Keio University, Tokyo.

出版信息

Jpn J Cancer Res. 1999 Jan;90(1):116-21. doi: 10.1111/j.1349-7006.1999.tb00674.x.

Abstract

R-94138, a matrix metalloproteinase inhibitor, was examined for the ability to prevent peritoneal dissemination of a human gastric cancer xenograft, TMK-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, the resulting peritoneal dissemination mimicked clinical carcinomatous peritonitis. When the maximum tolerated dose of mitomycin C (MMC) or cisplatin (DDP) was given 12 h after the tumor inoculation, peritoneal dissemination was completely inhibited, while the effect of R-94138 was limited when it was given i.p. at a dose of 20 mg/kg in a schedule of q.d. x 5 starting 12 h after 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 dissemination when it was administered i.p. at a dose of 30 mg/kg in a schedule of q.d. x 5 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 dissemination of gastric cancer.

摘要

R-94138是一种基质金属蛋白酶抑制剂,对其预防人胃癌异种移植瘤TMK-1腹膜播散的能力进行了研究。当TMK-1细胞与人正常成纤维细胞共培养的上清液进行明胶酶谱分析时,很明显R-94138抑制了MMP-2的蛋白表达。当以5×10(5)个细胞/只的剂量将TMK-1腹腔注射到裸鼠体内时,由此产生的腹膜播散模拟了临床癌性腹膜炎。当在肿瘤接种后12小时给予丝裂霉素C(MMC)或顺铂(DDP)的最大耐受剂量时,腹膜播散被完全抑制,而当在肿瘤注射后12小时开始以20mg/kg的剂量每日腹腔注射1次,共5次时,R-94138的效果有限。当在肿瘤接种后1周分别以2mg/kg和3mg/kg的单剂量腹腔注射MMC和DDP时,它们也能抑制腹膜播散。当从肿瘤注射后1周开始以30mg/kg的剂量每日腹腔注射1次,共5次时,R-94138能抑制腹膜播散。MMC与R-94138联合使用可增强对腹膜播散的预防效果。R-94138似乎是预防胃癌腹膜播散的一个有前途的候选药物。

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