Homeodomain protein CDX2 regulates COX-2 expression
in colorectal cancer
- Author(s)
- Sang-Pyo Kim; Jong-Wook Park; Sung-Hee Lee; Jun Hee Lim; Byeong-Churl Jang; Sang-Han Lee; In-Hwan Jang; Jean-Noel Freund; Seong-Il Suh; Kyo Cheol Mun; Dae-Kyu Song; Eun-Mi Ha; Won-Jae Lee; Taeg Kyu Kwon
- Keimyung Author(s)
- Kim, Sang Pyo; Park, Jong Wook; Jang, Byeong Churl; Suh, Seong Il; Mun, Kyo Cheol; Song, Dae Kyu; Kwon, Taeg Kyu
- Department
- Dept. of Pathology (병리학)
Dept. of Physiology (생리학)
Dept. of Biochemistry (생화학)
Dept. of Microbiology (미생물학)
Dept. of Molecular Medicine (분자의학)
Dept. of Immunology (면역학)
Institute for Medical Science (의과학연구소)
- Journal Title
- Biochemical and Biophysical Research Communications
- Issued Date
- 2004
- Volume
- 315
- Issue
- 1
- Abstract
- 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-κB. 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-κB and to inhibit p65-induced NF-κB minimal promoter activity in colon cancer cells. These results suggest that reduced CDX2 expression may be involved in colorectal carcinogenesis by enhancing NF-κB-mediated inflammatory genes such as COX-2.
Keywords
CDX2;
COX-2;
Expression;
Carcinogenesis;
Colorectal cancer
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