The Adenomatous Polyposis Coli (APC) gene was discovered through the identification of germline mutations in patients with familial APC and somatic mutations in patients with sporadic cases of colorectal carcinoma. We previously have demonstrated the existence of two large families with an attenuated form of APC, called AAPC. In AAPC families, gene carriers of the mutation develop fewer numbers of colorectal polyps than do patients with classical APC and if colorectal cancer occurs, the average age of onset in AAPC families occurs later than in APC. A hallmark feature of AAPC gene carriers is the large variation in adenomatous polyp number observed within the same family. We are interested in testing the hypothesis that this variation in phenotype is due to genes that modify the expression of the APC gene. Two loci have been identified that modify the murine APC phenotype (multiple intestinal neoplasia, MIN). The first locus, MOM-1, reduces the number and size of intestinal neoplasias that develop in Min mice. Secondly, a mutations in the murine methyltransferase gene also attenuates the Min phenotype. Three additional loci that alter the susceptibility to drug-induced (non-APC/MIN) tumorigenesis in mice also have been identified. In an attempt to discover modifying gene(s) in our two large, well characterized families, we will use genetic analysis to identify modifying loci. Our primary method of analysis will be the non-parametric linkage (NPL) method that does not require a specific genetic model. We will initially choose genetic markers in regions of the genome where candidate genes are known to reside. If any of these regions show evidence for suggestive linkage. we will then search for mutations within coding sequences of any candidate genes that localized to the critical region. If no positive or suggestive linkage results are found in this initial limited search, we will then carry out a complete genome-wide search for a modifying gene with a set of 300 highly polymorphic markers. Discovery of one or more major modifying loci of the APC gene would a significant advance in understanding the biochemical mechanisms of this important polyp-producing gene.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
1P01CA073992-01A1
Application #
6103343
Study Section
Project Start
1998-08-10
Project End
1999-05-31
Budget Start
Budget End
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Delker, Don A; Wood, Austin C; Snow, Angela K et al. (2018) Chemoprevention with Cyclooxygenase and Epidermal Growth Factor Receptor Inhibitors in Familial Adenomatous Polyposis Patients: mRNA Signatures of Duodenal Neoplasia. Cancer Prev Res (Phila) 11:4-15
Sample, Danielle C; Samadder, N Jewel; Pappas, Lisa M et al. (2018) Variables affecting penetrance of gastric and duodenal phenotype in familial adenomatous polyposis patients. BMC Gastroenterol 18:115
Fuller, Andrew K; Bice, Benjamin D; Venancio, Ashlee R et al. (2018) A Method to Define the Effects of Environmental Enrichment on Colon Microbiome Biodiversity in a Mouse Colon Tumor Model. J Vis Exp :
Bice, Benjamin D; Stephens, Megan R; Georges, Stephanie J et al. (2017) Environmental Enrichment Induces Pericyte and IgA-Dependent Wound Repair and Lifespan Extension in a Colon Tumor Model. Cell Rep 19:760-773
Jewel Samadder, N; Valentine, John F; Guthery, Stephen et al. (2017) Colorectal Cancer in Inflammatory Bowel Diseases: A Population-Based Study in Utah. Dig Dis Sci 62:2126-2132
Gan, Meng; Boothe, Dustin; Neklason, Deborah W et al. (2017) Outcomes and complications of radiation therapy in patients with familial adenomatous polyposis. J Gastrointest Oncol 8:643-649
Neklason, Deborah W; VanDerslice, James; Curtin, Karen et al. (2016) Evidence for a heritable contribution to neuroendocrine tumors of the small intestine. Endocr Relat Cancer 23:93-100
Samadder, N Jewel; Curtin, Karen; Pappas, Lisa et al. (2016) Risk of Incident Colorectal Cancer and Death After Colonoscopy: A Population-based Study in Utah. Clin Gastroenterol Hepatol 14:279-86.e1-2
Samadder, N Jewel; Neklason, Deborah W; Boucher, Kenneth M et al. (2016) Effect of Sulindac and Erlotinib vs Placebo on Duodenal Neoplasia in Familial Adenomatous Polyposis: A Randomized Clinical Trial. JAMA 315:1266-75
Li, Jun; Woods, Susan L; Healey, Sue et al. (2016) Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant. Am J Hum Genet 98:830-842

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