Antiproliferative activity of REIC/Dkk-3 and its significant down-regulation in non-small-cell lung carcinomas

被引:122
作者
Tsuji, T
Nozaki, I
Miyazaki, M
Sakaguchi, M
Pu, H
Hamazaki, Y
Iijima, O
Namba, M
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Cell Biol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med & Dent, Dept Surg Oncol & Thorac Surg, Okayama 7008558, Japan
[3] Okayama Univ, Grad Sch Med & Dent, Dept Surg Gastroenterol Transplant & Surg Oncol, Okayama 7008558, Japan
[4] Hisamitsu Pharmaceut Co Inc, Cent Res Ctr, Tsukuba, Ibaraki 3050856, Japan
关键词
D O I
10.1006/bbrc.2001.5972
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We recently reported the cloning of the REIC/Dkk-3 gene, whose expression was shown to be downregulated in many human immortalized and tumor-derived cell lines [T. Tsuji et al. (2000) Biochem. Biophys. Res. Commun. 268, 20-24]. In the present study, we demonstrated that expression of the exogenous REIC/Dkk-3 gene in tumor cells inhibited cell growth. Furthermore, the level of REIC/Dkk-3 mRNA in normal human cells was lowest in the late G, phase during the cell cycle. Then we found that the expression of REIC/Dkk-3 was significantly down-regulated in surgically resected non-small-cell lung carcinomas. We determined the REIC/Dkk-3 locus on chromosome 11p15, where loss of heterozygosity has frequently been observed in human tumors. These findings indicate that REIC/Dkk-3 may function as a tumor suppressor. (C) 2001 Academic Press.
引用
收藏
页码:257 / 263
页数:7
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