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Understanding Phenotypic Variation in Rodent Models with Germline Apc Mutations

Journal

CANCER RESEARCH
Volume 73, Issue 8, Pages 2389-2399

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-12-4607

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Funding

  1. National Cancer Institute from NIH [RO1 CA109220]
  2. National Center for Research Resources from NIH [P20 RR016475]
  3. National Institute of General Medical Sciences from NIH [P20 GM103418]

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Adenomatous polyposis coli (APC) is best known for its crucial role in colorectal cancer suppression. Rodent models with various Apc mutations have enabled experimental validation of different Apc functions in tumors and normal tissues. Since the development of the first mouse model with a germline Apc mutation in the early 1990s, 20 other Apc mouse and rat models have been generated. This article compares and contrasts currently available Apc rodent models with particular emphasis on providing potential explanations for their reported variation in three areas: (i) intestinal polyp multiplicity, (ii) intestinal polyp distribution, and (iii) extraintestinal phenotypes. Cancer Res; 73(8); 2389-99. (C) 2013 AACR.

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