Abstract
Objective: Oral squamous-cell carcinoma (OSCC) still has a poor prognosis. Lymph node metastasis (LNM) is a major determinant of treatment decisions and prognosis. Serine protease inhibitor Kazal-type 5 (SPINK5) is the inhibitor of kallikrein 5 (KLK5) and KLK7. SPINK5, KLK5 and KLK7 are three of the genes of a recently validated LNM-predicting gene expression profile in OSCC. This study evaluates their clinicopathological role and value as biomarkers in OSCC. Methods: Eighty-three patients with primary OSCC, treated surgically between 1996 and 2000, were included. Gene expression data were acquired from a previously reported study. Human papillomavirus (HPV) status was determined by an algorithm for HPV-16. Protein expression for KLK5, KLK7 and SPINK5 was semi-quantitatively determined in all 83 tumours by immunohistochemistry. All expression data were correlated with clinicopathological parameters. Results: Concurrent loss of KLK5 and KLK7 correlates with worse disease-specific and overall survival (DSS and OS). Multivariate analysis proved that co-expression is an independent prognostic factor for DSS (p = 0.029) and OS (p = 0.001). Conclusion: This report demonstrates that concurrent loss of KLK5 and KLK7 associates with a poor clinical outcome in OSCC and could therefore serve as prognostic marker in this disease.
Original language | English |
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Pages (from-to) | 58-67 |
Number of pages | 10 |
Journal | Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology |
Volume | 82 |
Issue number | 2 |
DOIs | |
Publication status | Published - Jul 2015 |
Keywords
- Oral squamous cell carcinoma
- Kallikrein 5
- Kallikrein 7
- Serine protease inhibitor Kazal-type 5
- LYMPH-NODE METASTASIS
- NECK-CANCER
- HUMAN-PAPILLOMAVIRUS
- OVARIAN-CANCER
- HEAD
- EXPRESSION
- BIOMARKERS
- ALGORITHM
- GENES
- LEKTI