Loss of heterozygosity on chromosome 11 in sporadic gastrinomas View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1992-06

AUTHORS

Mark P. Sawicki, Yu-Jui Yvonne Wan, Carey L. Johnson, James Berenson, Richard Gatti, Edward Passaro

ABSTRACT

Gastrinomas are pancreatic endocrine neoplasms that arise either sporadically or are inherited as part of the multiple endocrine neoplasia type I syndrome (MENI). Loss of heterozygosity (LOH) in the region flanking the MENI gene at chromosome 11q13 has been documented in a few sporadic and familial pancreatic endocrine tumors, but not previously in sporadic gastrinomas. It has therefore been suggested that gastrinomas develop by a mechanism different from other tumors associated with the MENI syndrome. We report LOH on chromosome 11 in 5 of 11 sporadic gastrinomas. Four of these tumors have LOH for markers flanking the MENI region. Molecular evaluation of segments of chromosomes 3, 13, and 17 known to contain cloned or putative tumor suppressor genes fail to show LOH except at one locus in one tumor. These data suggest that a tumor suppressor DNA segment exists at 11q13 that may be involved in the development of sporadic gastrinomas. More... »

PAGES

445-449

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00194320

DOI

http://dx.doi.org/10.1007/bf00194320

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1045674671

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/1352275


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