Abstract

High SERPINE1 expression is a common event in head and neck squamous cell carcinoma (HNSCC); however, whether it plays a role in determining clinical outcome remains still unknown. We studied SERPINE1 as a prognostic marker in two HNSCC patient cohorts. In a retrospective study (n = 80), high expression of SERPINE1 was associated with poor progression-free (p = 0.022) and cancer-specific (p = 0.040) survival. In a prospective study (n = 190), high SERPINE1 expression was associated with poor local recurrence-free (p = 0.022), progression-free (p = 0.002) and cancer-specific (p = 0.006) survival. SERPINE1 expression was identified as an independent risk factor for progression-free survival in patients treated with chemo-radiotherapy or radiotherapy (p = 0.043). In both patient cohorts, high SERPINE1 expression increased the risk of metastasis spread (p = 0.045; p = 0.029). The association between SERPINE1 expression and survival was confirmed using the HNSCC cohort included in The Cancer Genome Atlas project (n = 507). Once again, patients showing high expression had a poorer survival (p < 0.001). SERPINE1 over-expression in HNSCC cells reduced cell proliferation and enhanced migration. It also protected cells from cisplatin-induced apoptosis, which was accompanied by PI3K/AKT pathway activation. Downregulation of SERPINE1 expression had the opposite effect. We propose SERPINE1 expression as a prognostic marker that could be used to stratify HNSCC patients according to their risk of recurrence.

Highlights

  • Head and neck squamous cell carcinoma (HNSCC) is the sixth leading cancer in incidence worldwide [1, 2]

  • We identified SERPINE1 expression as a poor prognostic marker in head and neck squamous cell carcinoma

  • We used a third patient cohort of HNSCC (n = 507) included in The Cancer Genome Atlas (TCGA) database to support the association between SERPINE1 expression and patient survival

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Summary

Introduction

Head and neck squamous cell carcinoma (HNSCC) is the sixth leading cancer in incidence worldwide [1, 2]. The development of new predictive biomarkers could help to classify this heterogeneous group of tumors and improve treatment decision-making [5]. SERPINE1 (PAI-1) is the main regulator of the PA system, and it is involved in signal transduction, tumor growth, invasion and metastasis [9]. It is the main inhibitor of the plasminogen activators tPA and uPA. SERPINE1 expression has been validated as a marker for therapy decision making in patients with node-negative breast cancer [13, 14]

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