rdf:type |
|
lifeskim:mentions |
umls-concept:C0009402,
umls-concept:C0017262,
umls-concept:C0185117,
umls-concept:C0205245,
umls-concept:C0812382,
umls-concept:C1311076,
umls-concept:C1514873,
umls-concept:C1518174,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C2911684
|
pubmed:issue |
2
|
pubmed:dateCreated |
2004-4-9
|
pubmed:abstractText |
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.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/GLI3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Gli3 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Kruppel-Like Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, G-Protein-Coupled,
http://linkedlifedata.com/resource/pubmed/chemical/SMO protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Smo protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0304-3835
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
30
|
pubmed:volume |
207
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
205-14
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:15072830-Base Sequence,
pubmed-meshheading:15072830-Colorectal Neoplasms,
pubmed-meshheading:15072830-DNA Methylation,
pubmed-meshheading:15072830-DNA-Binding Proteins,
pubmed-meshheading:15072830-Heterozygote,
pubmed-meshheading:15072830-Humans,
pubmed-meshheading:15072830-Kruppel-Like Transcription Factors,
pubmed-meshheading:15072830-Molecular Sequence Data,
pubmed-meshheading:15072830-Mutation,
pubmed-meshheading:15072830-Nerve Tissue Proteins,
pubmed-meshheading:15072830-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:15072830-Promoter Regions, Genetic,
pubmed-meshheading:15072830-Receptors, G-Protein-Coupled,
pubmed-meshheading:15072830-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:15072830-Transcription Factors,
pubmed-meshheading:15072830-Tumor Cells, Cultured
|
pubmed:year |
2004
|
pubmed:articleTitle |
Functional Smoothened is required for expression of GLI3 in colorectal carcinoma cells.
|
pubmed:affiliation |
Sir Alastair Currie Cancer Research UK Laboratories, Division of Pathology, Molecular Medicine Centre, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XU, UK.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|