Down-regulation of the cytoglobin gene, located on 17q25, in tylosis with oesophageal cancer (TOC): evidence for trans-allele repression
| Autor: | Anthony Ellis, Lynn Rowbottom, Laura Hill, Joanne E. Langan, George Xinarianos, Triantafillos Liloglou, Janet M. Risk, Fiona E. McRonald, John K. Field, Joan M. Shaw |
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| Rok vydání: | 2006 |
| Předmět: |
Keratoderma
Palmoplantar Diffuse Male Esophageal Neoplasms Down-Regulation Locus (genetics) Biology Allelic Imbalance Cell Line Tumor Genetics medicine Humans Howel–Evans syndrome Allele Molecular Biology Genetics (clinical) Gene Expression Profiling Haplotype Cytoglobin Cancer General Medicine Sequence Analysis DNA medicine.disease Globins Tylosis Female Haploinsufficiency Chromosomes Human Pair 17 |
| Zdroj: | HUMAN MOLECULAR GENETICS |
| ISSN: | 0964-6906 |
| Popis: | Tylosis (focal non-epidermolytic palmoplantar keratoderma) is an autosomal dominant skin disorder that is associated with the early onset of squamous cell oesophageal cancer (SCOC) in three families. Our previous linkage and haplotype analyses have mapped the tylosis with oesophageal cancer (TOC) locus to a 42.5 kb region on chromosome 17q25 that has also been implicated in the aetiology of sporadically occurring SCOC from a number of different geographical populations. Oesophageal cancer is one of the 10 leading causes of cancer mortality worldwide. No inherited disease-causing mutations have been identified in the genes located in the 42.5 kb minimal region. We now show that cytoglobin gene expression in oesophageal biopsies from tylotic patients is dramatically reduced by approximately 70% compared with normal oesophagus. Furthermore, both alleles are equally repressed. Given the autosomal dominant nature of the disease, these results exclude haploinsufficiency as a mechanism of the disease and instead suggest a novel trans-allele interaction. We also show that the promoter is hypermethylated in sporadic oesophageal cancer samples: this may constitute the 'second hit' of a gene previously implicated in this disease by allelic imbalance studies. |
| Databáze: | OpenAIRE |
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