Homeodomain protein CDX2 regulates COX-2 expression in colorectal cancer

被引:46
作者
Kim, SP
Park, JW
Lee, SH
Lim, JH
Jang, BC
Lee, SH
Jang, IH
Freund, JN
Suh, SI
Mun, KC
Song, DK
Ha, EM
Lee, WJ [1 ]
Kwon, TK
机构
[1] Ewha Womans Univ, Div Mol Life Sci, Seoul 120750, South Korea
[2] Keimyung Univ, Inst Med Sci, Sch Med, Taegu 700712, South Korea
[3] Keimyung Univ, Sch Med, Chron Dis Res Ctr, Taegu 700712, South Korea
[4] Korea Res Inst Biosci & Biotechnol, Taejon 305333, South Korea
[5] INSERM, Strasbourg, France
关键词
CDX2; COX-2; expression; carcinogenesis; colorectal cancer;
D O I
10.1016/j.bbrc.2004.01.020
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
CDX2 is an intestine-specific tumor suppressor gene encoding homeodomain-containing transcription factor, which is involved in a variety of developmental, proliferating, and differentiating processes. Moreover, the expression of CDX2 is reduced in a subset of primary colorectal cancers. In contrast, cyclooxygenase-2 (COX-2) is often up-regulated in human colorectal cancers. However, the molecular relationship between CDX2 down-regulation and COX-2 up-regulation is unknown. Here we show that CDX2 down-regulates COX-2 promoter activity by interacting with NF-kappaB. The ectopic expression of CDX2 was found to suppress PMA-induced COX-2 promoter activity in a dose-dependent manner. In addition, the treatment of colorectal cancer cells with PMA resulted in significant reduction in the level of endogenous CDX2 and a significant increase in the level of endogenous COX-2, in a dose-dependent manner. Furthermore, CDX2 was found to co-immunoprecipitate with the p65 subunit of NF-kappaB and to inhibit p65-induced NF-kappaB minimal promoter activity in colon cancer cells. These results suggest that reduced CDX2 expression may be involved in colorectal carcinogenesis by enhancing NF-kappaB-mediated inflammatory genes such as COX-2. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:93 / 99
页数:7
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