Hippo-YAP signaling activation and cross-talk with PI3K in oral cancer: A retrospective cohort study

Oral Dis. 2024 Mar;30(2):149-162. doi: 10.1111/odi.14350. Epub 2022 Sep 16.

Abstract

Objectives: This study aimed to investigate the clinical and prognostic relevance of the Hippo-YAP transactivators YAP1 and TAZ in oral squamous cell carcinoma, and their possible relationship with PI3K/mTOR pathway activation.

Materials and methods: Immunohistochemical analysis of YAP1, TAZ, PIK3CA (p110α), p-AKT (Ser473), and p-S6 (Ser235) was performed in paraffin-embedded tissue specimens from 165 OSCC patients. Correlations between protein expression and clinical data were further assessed.

Results: YAP1 expression was detected in both cytoplasm and nucleus of tumor cells, whereas TAZ expression was only found in the nucleus. Nuclear YAP1 was significantly associated with tumor size (p = 0.03), neck lymph node metastasis (p = 0.02), TNM stage (p = 0.02), and poor differentiation (p = 0.04). Nuclear TAZ was associated with tobacco (p = 0.03) and alcohol consumption (p = 0.04), and poor tumor differentiation (p = 0.04). There was a positive significant correlation between nuclear and cytoplasmic YAP1, nuclear TAZ, p110α expression, and mTORC1 activation p-S6 (S235). Combined expression of nuclear and cytoplasmic YAP1 was prognostic in both univariate and multivariate analyses. Active nuclear YAP1 was significantly and independently associated with poor disease-specific (p = 0.005, HR = 2.520; 95% CI = 1.319-4.816) and overall survival (p = 0.015, HR = 2.126; 95% CI = 1.155-3.916).

Conclusion: Nuclear YAP1 is an independent predictor of poor survival in oral squamous cell carcinoma.

Keywords: PIK3CA; TAZ; YAP1; hippo-YAP pathway; oral squamous cell carcinoma; prognosis.

MeSH terms

  • Carcinoma, Squamous Cell* / pathology
  • Head and Neck Neoplasms*
  • Humans
  • Mouth Neoplasms* / metabolism
  • Phosphatidylinositol 3-Kinases
  • Retrospective Studies
  • Squamous Cell Carcinoma of Head and Neck
  • Transcription Factors / metabolism

Substances

  • Phosphatidylinositol 3-Kinases
  • Transcription Factors