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Cancer Lett ; 207(2): 205-14, 2004 Apr 30.
Article in English | MEDLINE | ID: mdl-15072830

ABSTRACT

We investigated a role for Hedgehog signalling in colon cancer by studying transcription of members of the pathway in human colorectal carcinoma cell lines. We determined the methylation status and screened the gene encoding the Hedgehog receptor-associated protein Smoothened (SMO) for putative mutations. In three cell lines lacking SMO expression the SMO promoter was fully methylated and the transcription factor GLI3 was not expressed. Two additional cell lines both having one methylated SMO allele and expressing mutant SMO did not express GLI3. Our results suggest that expression of wild-type SMO is required for expression of GLI3 by a mechanism that is independent of conventional Hedgehog signalling.


Subject(s)
Colorectal Neoplasms/genetics , DNA Methylation , DNA-Binding Proteins/metabolism , Mutation/genetics , Nerve Tissue Proteins , Receptors, G-Protein-Coupled/genetics , Transcription Factors/metabolism , Base Sequence , DNA-Binding Proteins/genetics , Heterozygote , Humans , Kruppel-Like Transcription Factors , Molecular Sequence Data , Polymorphism, Single-Stranded Conformational , Promoter Regions, Genetic/genetics , Reverse Transcriptase Polymerase Chain Reaction , Smoothened Receptor , Transcription Factors/genetics , Tumor Cells, Cultured , Zinc Finger Protein Gli3
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