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
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
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.