Review

Oncogene (2006) 25, 7522–7530. doi:10.1038/sj.onc.1210058

Wnt signaling and gastrointestinal tumorigenesis in mouse models

M M Taketo1

1Department of Pharmacology, Graduate School of Medicine, Kyoto University, Yoshida-Konoé-cho, Sakyo, Kyoto, Japan

Correspondence: Professor MM Taketo, Department of Pharmacology, Graduate School of Medicine, Kyoto University, Yoshida-Konoé-cho, Sakyo, Kyoto 606-8501, Japan. E-mail: taketo@mfour.med.kyoto-u.ac.jp

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Abstract

The canonical Wnt signaling plays important roles in embryonic development and tumorigenesis. For the latter, induced mutations in mice have greatly contributed to our understanding of the molecular mechanisms of cancer initiation and progression. Here, I will review recent reports on gastrointestinal cancer model mice, with an emphasis on the roles of the Wnt signal pathway. They include: mouse models for familial adenomatous polyposis; modifying factors that affect mouse intestinal polyposis, including the genes that help cancer progression; Wnt target genes that affect mouse intestinal polyposis; and a mouse model of gastric cancer that mimics Helicobacter pyroli infection.

Keywords:

Wnt, Apc, beta-catenin, colon cancer, gastric cancer

Abbreviations:

AA, arachidonic acid; ABI, anaphase bridge index; ACF, aberrant crypt foci; Chr, (mouse) chromosome; CIN, chromosomal instability; cM, centimorgan(s); COX, cyclooxygenase; FAP, familial adenomatous polyposis; GI, gastrointestinal; HDAC, histone deacetylase; HNPCC, hereditary nonpolyposis colon cancer; IL, interleukin; K19, cytokeratin 19; LOH, loss of heterozygosity; MSI, microsatellite instability; NSAID, non-steroidal anti-inflammatory drug; PG, prostaglandin; mPGES, microsomal prostaglandin E synthase; PI, phosphoinositide; PLA2, phospholipase A2; PPAR, peroxysome proliferator activator receptor; SPEM, spasmolytic polypeptide/trefoil factor 2-expressing metaplasia; TCF, T-cell factor; TFF, trefoil factor; Tg, transgenic

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