Kennedy A R
Department of Radiation Oncology, University of Pennsylvania School of Medicine, Philadelphia 19104.
Prev Med. 1993 Sep;22(5):796-811. doi: 10.1006/pmed.1993.1073.
There is now compelling evidence that certain protease inhibitors have strong anticarcinogenic activity. A particular protease inhibitor derived from soybeans, the Bowman-Birk inhibitor, appears to be highly promising as a cancer chemopreventive agent. In this article, studies performed to characterize an extract of soybeans containing the Bowman-Birk inhibitor, termed Bowman-Birk inhibitor concentrate, are described.
A number of different methods have been utilized to evaluate the efficacy and safety of Bowman-Birk inhibitor concentrate as a cancer chemopreventive agent in cells and animals. Bowman-Birk inhibitor concentrate has been studied extensively in animal carcinogenesis model systems and in vitro transformation systems.
Bowman-Birk inhibitor has been shown to prevent animal carcinogenesis in the absence of adverse side effects in several different systems. The dose proposed for human trials is approximately two orders of magnitude below doses shown to have no adverse effects in animal studies. At high doses, Bowman-Birk inhibitor concentrate has been shown to have a life-lengthening effect in mice. The intermediate marker endpoints known to be affected by Bowman-Birk inhibitor/Bowman-Birk inhibitor concentrate in in vitro and in vivo models systems include levels of oncogene expression and proteolytic activity. These intermediate marker endpoints, as well as histopathology, have been proposed for use in projected human trials which will be performed to evaluate Bowman-Birk inhibitor concentrate as an anticarcinogenic agent.
Bowman-Birk inhibitor concentrate is now ready for human trials and is likely to emerge as a powerful chemopreventive agent for human cancer.
目前有确凿证据表明某些蛋白酶抑制剂具有强大的抗癌活性。一种从大豆中提取的特定蛋白酶抑制剂——鲍曼-伯克抑制剂,作为一种癌症化学预防剂似乎极具前景。本文描述了为表征一种含有鲍曼-伯克抑制剂的大豆提取物(称为鲍曼-伯克抑制剂浓缩物)而进行的研究。
已采用多种不同方法来评估鲍曼-伯克抑制剂浓缩物作为细胞和动物癌症化学预防剂的疗效和安全性。鲍曼-伯克抑制剂浓缩物已在动物致癌模型系统和体外转化系统中得到广泛研究。
在几个不同的系统中,鲍曼-伯克抑制剂已被证明可预防动物致癌且无不良副作用。拟用于人体试验的剂量比在动物研究中显示无不良影响的剂量低约两个数量级。在高剂量下,鲍曼-伯克抑制剂浓缩物已被证明对小鼠有延长寿命的作用。在体外和体内模型系统中已知受鲍曼-伯克抑制剂/鲍曼-伯克抑制剂浓缩物影响的中间标记终点包括癌基因表达水平和蛋白水解活性。这些中间标记终点以及组织病理学已被提议用于即将进行的人体试验,以评估鲍曼-伯克抑制剂浓缩物作为抗癌剂的效果。
鲍曼-伯克抑制剂浓缩物现已准备好进行人体试验,并且很可能成为一种强大的人类癌症化学预防剂。