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每日一次口服库尼茨型蛋白酶抑制剂比昆宁在小鼠模型和人类癌症中的治疗效果。

Therapeutic efficacy of once-daily oral administration of a Kunitz-type protease inhibitor, bikunin, in a mouse model and in human cancer.

作者信息

Kobayashi Hiroshi, Yagyu Tatsuo, Inagaki Kiyokazu, Kondo Toshiharu, Suzuki Mika, Kanayama Naohiro, Terao Toshihiko

机构信息

Department of Obstetrics and Gynecology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Cancer. 2004 Feb 15;100(4):869-77. doi: 10.1002/cncr.20034.

Abstract

BACKGROUND

Bikunin, a Kunitz-type protease inhibitor, specifically inhibits tumor invasion and metastasis.

METHODS

The authors initially evaluated the therapeutic efficacy of once-daily oral administration of different doses of bikunin against human ovarian carcinoma HRA cells growing in the peritonea of nude mice. For the in vivo studies, female 7-week-old nude mice were randomized to 1 of 4 groups: bikunin-treated groups (n = 9 in each group) received 3, 10, or 30 microg/g body weight per day bikunin for 7 days via gastrointestinal gavage, and a control group (n = 9) received the vehicle solution (phosphate-buffered saline) via gastrointestinal gavage. On Day 9, the abdominal cavity was examined by two observers who were blinded to treatment.

RESULTS

After oral administration, intact bikunin was detectable in mouse serum specimens at 3 and 6 hours. This was followed by a decline at 12 hours. The mice given bikunin at the highest dose level had a 40% decrease in tumor load. The highest uptake in the tumor was obtained with [125I]bikunin 12 hours postadministration. No effect on either food intake or body weight was observed in the treated versus sham groups. The current study was the first to report the potent activity of once-daily oral administration of bikunin against ovarian carcinoma. Next, the authors performed a Phase I trial to determine the maximum-tolerated dose (MTD) and safety of a once-daily oral administration schedule. The indication was locally advanced uterine cervical carcinoma after definitive treatment. An escalating dose (3, 10, and 30 mg/kg per day) of bikunin was administered orally to nine patients for 7 days. There were no dose-limiting toxicities and the MTD of the bikunin schedule was not defined. The authors also obtained preliminary data on its effect on urokinase-type plasminogen activator expression at the highest dose level.

CONCLUSIONS

Once-daily oral administration of bikunin was found to be safe in humans and exhibited signs of biologic activity.

摘要

背景

比库宁是一种库尼茨型蛋白酶抑制剂,可特异性抑制肿瘤侵袭和转移。

方法

作者首先评估了每日一次口服不同剂量比库宁对裸鼠腹膜内生长的人卵巢癌HRA细胞的治疗效果。在体内研究中,将7周龄雌性裸鼠随机分为4组中的1组:比库宁治疗组(每组n = 9)通过胃肠道灌胃每天接受3、10或30μg/g体重的比库宁,持续7天,对照组(n = 9)通过胃肠道灌胃接受赋形剂溶液(磷酸盐缓冲盐水)。在第9天,由两名对治疗不知情的观察者检查腹腔。

结果

口服后,在3小时和6小时的小鼠血清标本中可检测到完整的比库宁。随后在12小时时下降。给予最高剂量水平比库宁的小鼠肿瘤负荷降低了40%。给药后12小时,[125I]比库宁在肿瘤中的摄取量最高。在治疗组与假手术组中,未观察到对食物摄入量或体重的影响。本研究首次报道了每日一次口服比库宁对卵巢癌的强效活性。接下来,作者进行了一项I期试验,以确定每日一次口服给药方案的最大耐受剂量(MTD)和安全性。适应症为确定性治疗后的局部晚期子宫颈癌。对9名患者口服递增剂量(每天3、10和30mg/kg)的比库宁,持续7天。没有剂量限制性毒性,比库宁给药方案的MTD未确定。作者还获得了其在最高剂量水平对尿激酶型纤溶酶原激活剂表达影响的初步数据。

结论

发现每日一次口服比库宁对人体安全,并表现出生物活性迹象。

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