Taketo M M
Laboratory of Biomedical Genetics, Graduate School of Pharmaceutical Sciences, University of Tokyo, Japan.
Inflamm Res. 1998 Oct;47 Suppl 2:S112-6. doi: 10.1007/s000110050295.
The role of cyclooxygenase-2 (COX-2) in colorectal tumorigenesis in mice was studied by Oshima et al. to determine the effects of COX-2 gene knockouts and a new COX-2 inhibitor. In the study, heterozygous Apcdelta716 knockout mice, a mouse model of human familial adenomatous polyposis (FAP), were either crossed to COX-2 gene knockout mice, or fed chow containing the COX-2-selective inhibitor. Apcdelta716 litter mates were used as positive controls, which developed 652+/-198 (SD) polyps at 10 weeks. Introduction of a COX-2 gene mutation, or feeding with the COX-2-selective inhibitor to the Apcdelta716 knockout mice, reduced the number and size of intestinal polyps dramatically. The results provide direct genetic evidence that COX-2 plays a key role in tumorigenesis, and indicate that COX-2-selective inhibitors can be a new class of therapeutic agents for colorectal polyposis and cancer.
大岛等人研究了环氧化酶 - 2(COX - 2)在小鼠结直肠癌发生中的作用,以确定COX - 2基因敲除和一种新型COX - 2抑制剂的效果。在该研究中,人类家族性腺瘤性息肉病(FAP)的小鼠模型——杂合子Apcdelta716基因敲除小鼠,要么与COX - 2基因敲除小鼠杂交,要么喂食含COX - 2选择性抑制剂的食物。Apcdelta716同窝小鼠用作阳性对照,其在10周时出现652±198(标准差)个息肉。将COX - 2基因突变引入Apcdelta716基因敲除小鼠,或用COX - 2选择性抑制剂喂食它们,可显著减少肠道息肉的数量和大小。这些结果提供了直接的遗传学证据,表明COX - 2在肿瘤发生中起关键作用,并表明COX - 2选择性抑制剂可能成为一类用于治疗结直肠息肉病和癌症的新型治疗药物。