4.6 Article

Sonic Hedgehog Acts as a Negative Regulator of β-Catenin Signaling in the Adult Tongue Epithelium

Journal

AMERICAN JOURNAL OF PATHOLOGY
Volume 177, Issue 1, Pages 404-414

Publisher

ELSEVIER SCIENCE INC
DOI: 10.2353/ajpath.2010.091079

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Funding

  1. Deutsche Forschungsgemeinschaft [P1 158/7-3]
  2. SFB [TR23, B7]
  3. Excellence Cluster Cardio-Pulmonary System
  4. LOEWE Initiative Hessen
  5. Onkogene Signaltransduktion Frankfurt (OSF) [III L 4-518/55.004, 2009]
  6. EU

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Wnt/beta-catenin signaling has been implicated in taste papilla development; however, its role in epithelial maintenance and tumor progression in the adult tongue remains elusive. We show Wnt/beta-catenin pathway activation in reporter mice and by nuclear beta-catenin staining in the epithelium and taste papilla of adult mouse and human tongues. beta-Catenin activation in APC(min/+) mice, which carry a mutation in adenomatous poliposis coli (APC), up-regulates Sonic hedgehog (Shh) and Jagged-2 (JAG2) in the tongue epithelium without formation of squamous cell carcinoma (SCC). We demonstrate that Shh suppresses beta-catenin transcriptional activity in a signaling-dependent manner in vitro and in vivo. A similar regulation and function was observed for JAG2, suggesting that both pathways negatively regulate beta-catenin, thereby preventing SCC formation in the tongue. This was supported by reduced nuclear beta-catenin in the tongue epithelium of Patched(+/-) mice, exhibiting dominant active Shh signaling. At the invasive front of human tongue cancer, nuclear beta-catenin and Shh were increased, suggesting their participation in tumor progression. Interestingly, Shh but not JAG2 was able to reduce beta-catenin signaling in SCC cells, arguing for a partial loss of negative feedback on beta-catenin transcription in tongue cancer. We show for the first time that the putative Wnt/beta-catenin targets Shh and JAG2 control beta-catenin signaling in the adult tongue epithelium, a function that is partially lost in lingual SCC. (Am J Pathol 2010, 177:404-414; DOI: 10.2353/ajpath.2010.091079)

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