Dang Duyen T, Chen Xinming, Feng Jing, Torbenson Michael, Dang Long H, Yang Vincent W
Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Oncogene. 2003 May 29;22(22):3424-30. doi: 10.1038/sj.onc.1206413.
Krüppel-like factor 4 (KLF4) is a zinc-finger-containing transcription factor, the expression of which is enriched in the postmitotic cells of the intestinal epithelium. KLF4 is a target gene of the tumor suppressor adenomatous polyposis coli (APC). We sought to determine the role of KLF4 in suppressing the tumorigenecity of RKO colon cancer cells, which do not express KLF4. We utilized an established system in RKO cells, in which an inducible promoter controls expression of KLF4. Four independent assays were used to assess the effects of KLF4 induction on tumor cells. We find that KLF4 overexpression reduces colony formation, cell migration and invasion, and in vivo tumorigenecity. The mechanism of action of KLF4 does not involve apoptosis. These findings, along with our previous findings that KLF4 induces G1/S arrest, suggest that KLF4 is a cell cycle checkpoint protein that can reduce tumorigenecity of colon cancer cells.
Krüppel样因子4(KLF4)是一种含锌指的转录因子,其表达在肠上皮的有丝分裂后细胞中富集。KLF4是肿瘤抑制因子腺瘤性息肉病基因(APC)的一个靶基因。我们试图确定KLF4在抑制不表达KLF4的RKO结肠癌细胞致瘤性中的作用。我们在RKO细胞中利用了一个既定系统,其中一个诱导型启动子控制KLF4的表达。使用了四种独立的测定方法来评估KLF4诱导对肿瘤细胞的影响。我们发现KLF4的过表达减少了集落形成、细胞迁移和侵袭以及体内致瘤性。KLF4的作用机制不涉及细胞凋亡。这些发现,连同我们之前发现KLF4诱导G1/S期阻滞,表明KLF4是一种细胞周期检查点蛋白,可降低结肠癌细胞的致瘤性。