Aberrant β-Catenin and Lef1 Expression May Predict the Clinical Outcome for Patients with Oropharyngeal Cancer

Author:

Papagerakis P.1,Pannone G.2,Shabana A-H.3,Depondt J.34,Santoro A.2,Ghirtis K.15,Berdal A.3,Papagerakis S.35

Affiliation:

1. Department of Orthodontics and Pediatric Dentistry, University of Michigan Ann Arbor, MI, USA

2. Department of Surgical Sciences — Section of Pathology, University of Foggia, Foggia, Italy

3. Orofacial Biology and Pathology Laboratory, INSERM UMRS872, Paris University 7, Cordeliers Research Centre, Paris, France

4. Department of Otolaryngology - Head & Neck Surgery, Hospital Bichat, Paris, France

5. Department of Otolaryngology - Head and Neck Surgery, University of Michigan Ann Arbor, MI, USA

Abstract

β-catenin, normally expressed on the epithelial cell surface, plays a crucial role in cadherin-mediated cell adhesion. Recent evidence suggests that β-catenin is also involved in other functions such as intracellular signaling via the Wnt pathway by creating a nuclear complex with members of the Lymphoid-Enhancer-Factor/T-Cell-Factor (LEF/TCF) family of transcription factors, and gene regulation that it is implicated in the development of several tumors. Little information is available on β-catenin expression and its main partner in the Wnt signaling pathway, LEF1, in oropharyngeal squamous cell carcinomas (OP-SCCs). The aim of this study is to investigate the expression of β-catenin and LEF1 expression in human primary OP-SCCs and to evaluate their clinical and prognostic significance. OP-SCCs and normal peritumoral areas were analyzed by immunohistochemistry, Western-blot and RT-PCR. β-catenin was overexpressed in tumors in comparison to normal peritumoral areas and displayed predominantly intracellular (cytosolic/nuclear) localization in 62% of the tumors. Immunoreactivity was correlated with clinicopathological parameters and long-term follow-up, and a significant association was found between protein expression and development of local recurrences (P =0.03). The OP-SCCs with poor clinical outcome, which displayed intracellular β-catenin expression, were also strongly positive for LEF1, with their co-expression statistically significant (P = 0.040). All (100%) advanced (stages 3+4) SCCs, 66.7% of the SCCs with positive lymph nodes and 80% of the SSCs that developed local recurrences were LEF1 positive. Cox regression analysis confirmed a poorer overall survival in cases with high expression of β-catenin and LEF1. Our results suggest that assessing intracellular β-catenin and LEF1 expression might help in patient risk stratification and outcome prediction, and serve as novel therapeutic targets in advanced OP-SCC.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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