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J Biol Chem ; 277(39): 35795-800, 2002 Sep 27.
Article in English | MEDLINE | ID: mdl-12124393

ABSTRACT

CDX1 is a homeobox protein that inhibits proliferation of intestinal epithelial cells and regulates intestine-specific genes involved in differentiation. CDX1 expression is developmentally and spatially regulated, and its expression is aberrantly down-regulated in colorectal cancers and colon cancer-derived cell lines. However, very little is known about the molecular mechanism underlying the regulation of CDX1 gene expression. In this study, we characterized the CDX1 gene structure and identified that its gene promoter contained a typical CpG island with a CpG observed/expected ratio of 0.80, suggesting that the CDX1 gene is a target of aberrant methylation. Alterations of DNA methylation in the CDX1 gene promoter were investigated in a series of colorectal cancer cell lines. Combined Bisulfite Restriction Analysis (COBRA) and bisulfite sequencing analysis revealed that the CDX1 promoter is methylated in CDX1 non-expressing colorectal cancer cell lines but not in human normal colon tissue and T84 cells, which express CDX1. Treatment with 5'-aza-2'-deoxycytidine (5-azaC), a DNA methyltransferase inhibitor, induced CDX1 expression in the colorectal cancer cell lines. Furthermore, de novo methylation was determined by establishing stably transfected clones of the CDX1 promoter in SW480 cells and demethylation by 5-azaC-activated reporter gene expression. These results indicate that aberrant methylation of the CpG island in the CDX1 promoter is one of the mechanisms that mediate CDX1 down-regulation in colorectal cancer cell lines.


Subject(s)
Azacitidine/analogs & derivatives , Colorectal Neoplasms/genetics , DNA Methylation , Down-Regulation , Animals , Azacitidine/pharmacology , Base Sequence , Blotting, Western , Cloning, Molecular , Colorectal Neoplasms/metabolism , Cosmids/metabolism , CpG Islands , Decitabine , Enzyme Inhibitors/pharmacology , HeLa Cells , Humans , Mice , Molecular Sequence Data , Plasmids/metabolism , Promoter Regions, Genetic , Reverse Transcriptase Polymerase Chain Reaction , Sulfites/pharmacology , Transfection , Tumor Cells, Cultured
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