LACK OF ALLELIC LOSS AT THE MULTIPLE ENDOCRINE NEOPLASIA TYPE 1(MEN-1) GENE LOCUS IN A PANCREATIC DUCTAL (NONENDOCRINE) ADENOCARCINOMA OF APATIENT WITH THE MEN-1 SYNDROME

Citation
C. Bordi et al., LACK OF ALLELIC LOSS AT THE MULTIPLE ENDOCRINE NEOPLASIA TYPE 1(MEN-1) GENE LOCUS IN A PANCREATIC DUCTAL (NONENDOCRINE) ADENOCARCINOMA OF APATIENT WITH THE MEN-1 SYNDROME, Virchows Archiv, 426(2), 1995, pp. 203-208
Citations number
31
Categorie Soggetti
Pathology
Journal title
ISSN journal
09456317
Volume
426
Issue
2
Year of publication
1995
Pages
203 - 208
Database
ISI
SICI code
0945-6317(1995)426:2<203:LOALAT>2.0.ZU;2-7
Abstract
The gene responsible for multiple endocrine neoplasia type I(MEN-1) sy ndrome has been mapped to chromosome 11q13. It appears to function as a tumour-suppressor gene analogous to that for retinoblastoma and alle lic losses involving the wild-type of the MEN-1 allele have been found in parathyroid and pancreatic endocrine tumours of MEN-1 patients. No genetic information has been provided so far on non-endocrine maligna ncies that may occur in MEN-1 patients. A case of exocrine pancreatic adenocarcinoma presenting as the terminal event in a woman with a long standing history of MEN-1 syndrome and multiple endocrine tumours of the pancreas was investigated for possible allelic losses at the MEN-1 gene locus using restriction fragment length polymorphisms (RFLPs) cl osely linked to the MEN-I gene and polymerase chain reaction (PCR) for D11S533 locus. No allelic losses were found in tumour tissue with two informative RFLPs (D11S97, D11S146) or with PCR analysis. These findi ngs suggest that the MEN-1 gene does not confer a predisposition to de velop tumours other than those that typify the syndrome.