Multiple intestinal neoplasia caused by a mutation in the murine homolog of the APC gene

Li Kuo Su, Kenneth W. Kinzler, Bert Vogelstein, Antoinette C. Preisinger, Amy Rapaich Moser, Cindy Luongo, Karen A. Gould, William F. Dove

Research output: Contribution to journalArticlepeer-review

1258 Scopus citations

Abstract

Germ-line mutations of the APC gene are responsible for familial adenomatous polyposis (FAP), an autosomal dominantly inherited disease in humans. Patients with FAP develop multiple benign colorectal tumors. Recently, a mouse lineage that exhibits an autosomal dominantly inherited predisposition to multiple intestinal neoplasia (Min) was described. Linkage analysis showed that the murine homolog of the APC gene (mApc) was tightly linked to the Min locus. Sequence comparison of mApc between normal and Min-affected mice identified a nonsense mutation, which cosegregated with the Min phenotype. This mutation is analogous to those found in FAP kindreds and in sporadic colorectal cancers.

Original languageEnglish (US)
Pages (from-to)668-670
Number of pages3
JournalScience
Volume256
Issue number5057
DOIs
StatePublished - 1992
Externally publishedYes

ASJC Scopus subject areas

  • General

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