Torrance C J, Jackson P E, Montgomery E, Kinzler K W, Vogelstein B, Wissner A, Nunes M, Frost P, Discafani C M
The Howard Hughes Medical Institute and The Johns Hopkins Oncology Center, Baltimore, Maryland 21231, USA.
Nat Med. 2000 Sep;6(9):1024-8. doi: 10.1038/79534.
A combination of two drugs afforded remarkable protection from intestinal neoplasia in APC(Min/+) mice, a murine model of human familial adenomatous polyposis (FAP). One of the drugs was sulindac, a prototypical non-steroidal anti-inflammatory drug with established chemopreventative activity. The second drug was EKI-569, a newly developed, irreversible inhibitor of the epidermal growth factor receptor kinase. Although 100% of the untreated APC(Min/+) mice developed approximately 20 polyps, nearly half the mice treated with these two agents developed no polyps at all. These results suggest a powerful strategy for the chemoprevention of human colonic neoplasia.
在人类家族性腺瘤性息肉病(FAP)的小鼠模型APC(Min/+)中,两种药物的联合使用为肠道肿瘤形成提供了显著的保护作用。其中一种药物是舒林酸,一种具有既定化学预防活性的典型非甾体抗炎药。第二种药物是EKI-569,一种新开发的表皮生长因子受体激酶不可逆抑制剂。尽管100%未治疗的APC(Min/+)小鼠长出了约20个息肉,但用这两种药物治疗的小鼠中近一半根本没有长出息肉。这些结果提示了一种预防人类结肠肿瘤形成的有效策略。