Kennedy A R, Beazer-Barclay Y, Kinzler K W, Newberne P M
Department of Radiation Oncology, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.
Cancer Res. 1996 Feb 15;56(4):679-82.
We have performed experiments to determine whether the soybean-derived protease inhibitor, Bowman-Birk inhibitor (BBI), has the ability to affect intestinal carcinogenesis in Min mice. Min mice have an autosomally dominantly inherited predisposition to multiple intestinal neoplasms and are known to have a very high spontaneous rate of tumor development in both the small intestine and colon. BBI was administered in the diet as BBI Concentrate (BBIC), the form of BBI which is currently being evaluated in human trials as a cancer chemopreventive agent. We observed that 0.5% dietary BBIC led to a 42-50% reduction in the number of tumors/mouse in the small intestine and colon and a 41% reduction of tumorigenesis in the colon when the data are analyzed in terms of the fraction of mice bearing tumors. Thus, tumor-development in both the small intestine and colon of Min mice can be significantly suppressed by BBIC, despite the fact that the animals carry a predisposing mutation that leads to a markedly increased intestinal tumor incidence and mortality rate.
我们进行了实验,以确定源自大豆的蛋白酶抑制剂——鲍曼-伯克抑制剂(BBI)是否具有影响Min小鼠肠道癌变的能力。Min小鼠具有常染色体显性遗传的多发性肠道肿瘤易感性,并且已知在小肠和结肠中都有非常高的自发肿瘤发生率。BBI以BBI浓缩物(BBIC)的形式添加到饮食中,BBIC是目前正在人体试验中作为癌症化学预防剂进行评估的BBI形式。我们观察到,当根据携带肿瘤的小鼠比例分析数据时,饮食中0.5%的BBIC可使小肠和结肠中每只小鼠的肿瘤数量减少42%-50%,结肠中的肿瘤发生率降低41%。因此,尽管这些动物携带导致肠道肿瘤发生率和死亡率显著增加的易感突变,但BBIC仍可显著抑制Min小鼠小肠和结肠中的肿瘤发展。