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Tumor progression in Apc1638N mice with Exo1 and Fen1 deficiencies

Oncogene volume 26, pages 6297–6306 (2007)Cite this article

Abstract

Flap endonuclease 1 (Fen1) and exonuclease 1 (Exo1) have sequence homology and similar nuclease capabilities. Both function in multiple pathways of DNA metabolism, but appear to have distinct in vivo nucleic acid substrates, and therefore distinct metabolic roles. When combined with Apc1638N, Fen1 promotes tumor progression. Because of functional similarity to Fen1, and because Exo1 is involved in DNA mismatch repair (MMR) by interaction with Msh2 and Mlh1, genes that cause hereditary nonpolyposis colorectal cancer (HNPCC), we investigated the possibility that Exo1 might also act as a modifier to Apc1638N. We present evidence that mice with combined mutations in Apc1638N and Exo1 and Apc1638N, Exo1 and Fen1 genes show moderate increased tumor incidence and multiplicity in comparison to Apc1638N siblings, implying a low penetrance role for Exo1 in early gastrointestinal (GI) tumorigenesis. Despite a decrease in median survival (10 months) in Apc1638N Exo1 mice, their tumors do not progress any more rapidly than those of Apc1638N. Instead these animals die from infections that are the result of impaired immune response. Apc1638N Exo1 Fen1 mice survive longer (18 months), and therefore appear relatively immune competent. They die of invasive GI tumors that display microsatellite instability (MSI). Our results show that Exo1 has a modest tumor suppressor function.

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Acknowledgements

This work is supported by NIH grants CA-084301 and NIEHS grant ES-011040 (RS Kucherlapati).

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Authors and Affiliations

  1. Harvard-Partners Center for Genetics and Genomics, Harvard Medical School, Boston, MA, USA

    M Kucherlapati, A Nguyen, M Kuraguchi & R Kucherlapati

  2. Strang Cancer Research Laboratory at the Rockefeller University, New York, NY, USA

    K Yang, K Fan & M Lipkin

  3. Rodent Histopathology Core, Harvard Medical School, Boston, MA, USA

    R Bronson

  4. Department of Pathology, Tufts University Schools of Medicine and Veterinary Medicine, Boston, MA, USA

    R Bronson

  5. Department of Cell Biology, Albert Einstein College of Medicine, Bronx, NY, USA

    K Wei & W Edelmann

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  1. M Kucherlapati
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  2. A Nguyen
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Correspondence to M Kucherlapati.

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Kucherlapati, M., Nguyen, A., Kuraguchi, M. et al. Tumor progression in Apc1638N mice with Exo1 and Fen1 deficiencies. Oncogene 26, 6297–6306 (2007). https://doi.org/10.1038/sj.onc.1210453

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