PMID- 11960210 OWN - NLM STAT- MEDLINE DCOM- 20020905 LR - 20061115 IS - 0364-2313 (Print) IS - 0364-2313 (Linking) VI - 26 IP - 7 DP - 2002 Jul TI - Deletion of chromosome 1, but not mutation of MEN-1, predicts prognosis in sporadic pancreatic endocrine tumors. PG - 843-7 AB - Pancreatic endocrine tumors (PETs) may be sporadic or inherited in the multiple endocrine neoplasia type 1 (MEN-1) syndrome. The inherited form is caused by mutations of the MEN-1 gene, which functions as a tumor suppressor gene and maps to chromosome 11q13. These tumors tend to have a better prognosis than their sporadic counterparts, which often have mutations of the MEN-1 gene. Previous molecular analyses of sporadic PETs suggest a high frequency of loss of heterozygosity (LOH) at chromosome 1 as well as mutation of MEN-1. In this study we correlate abnormalities of MEN-1 and chromosome 1 LOH with the biological behavior of sporadic PETs. Loss of heterozygosity for markers at chromosome 11q13 and mutation of MEN-1 were equally frequent in tumors with or without liver metastases. Mutation of MEN-1 is more frequent in gastrinomas than in non-gastrinomas. Loss of heterozygosity for markers on chromosome 1 is more frequent in PETs with liver metastases. These results suggest a molecular tumor model in which there is a dichotomy in the development of benign and malignant PETs. FAU - Guo, Sydney S AU - Guo SS AD - Department of Surgery, West Los Angeles VA Medical Center and the UCLA School of Medicine, Los Angeles, CA 90073, USA. FAU - Wu, Alan Y AU - Wu AY FAU - Sawicki, Mark P AU - Sawicki MP LA - eng PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. DEP - 20020418 PL - United States TA - World J Surg JT - World journal of surgery JID - 7704052 RN - 0 (MEN1 protein, human) RN - 0 (Neoplasm Proteins) RN - 0 (Proto-Oncogene Proteins) SB - IM MH - Adenoma, Islet Cell/diagnosis/*genetics/pathology MH - Carcinoma, Islet Cell/diagnosis/genetics/pathology MH - Chromosome Deletion MH - Chromosomes, Human, Pair 1/*genetics MH - Chromosomes, Human, Pair 11/*genetics MH - Humans MH - Liver Neoplasms/secondary MH - Loss of Heterozygosity MH - Multiple Endocrine Neoplasia Type 1/*genetics MH - Mutation MH - Neoplasm Metastasis MH - Neoplasm Proteins/*genetics MH - Pancreatic Neoplasms/diagnosis/*genetics/pathology MH - Prognosis MH - *Proto-Oncogene Proteins EDAT- 2002/04/18 10:00 MHDA- 2002/09/06 10:01 CRDT- 2002/04/18 10:00 PHST- 2002/04/18 10:00 [pubmed] PHST- 2002/09/06 10:01 [medline] PHST- 2002/04/18 10:00 [entrez] AID - 10.1007/s00268-002-4062-4 [doi] PST - ppublish SO - World J Surg. 2002 Jul;26(7):843-7. doi: 10.1007/s00268-002-4062-4. Epub 2002 Apr 18.