Abstract

BackgroundSimple epithelial keratins appear early during embryonic development and are expressed in non-stratified, ductal and pseudo-stratified epithelial tissues. CK19, the lowest molecular weight keratin, is also expressed in basal layer of squamous epithelia of mucosal surfaces. Previous studies have shown that High Risk-Human Papilloma Virus (HR-HPV) epithelial infection induces cell immortalization via E6 and E7 viral proteins and this, in turn, impairs cytokeratin expression in cancerous cells lines derived from uterine cervix. Here, we demonstrate the possible relationship between HR-HPV+ oral/oropharyngeal cancer and the high levels of CK19 expression.MethodsWe analyzed 38 cases of Oral Squamous Cell Carcinomas/ Oro-Pharyngeal Squamous Cell Carcinomas (OSCCs/OPSCCs) by Immunohistochemistry (IHC) using specific antibody (Ab) detecting CK19, by In Situ Hybridization (ISH) and Polymerase Chain Reaction (PCR) based methods in order to define the HPV infectious status. We also evaluated the variation of CK19 expression in UPCI-SCC-131 (HPV−) and UPCI-SCC-154 (HPV+) cell lines by immunocytochemistry (ICC) and flow cytometry.ResultsCK19 OSCC/OPSCC score has been identified multiplying percentage of cancer expressing cells to staining intensity. CK19 expression score in OSCCs/OPSCCs was very different between HPV+ (mean: 288.0 ± 24.3) and HPV− cancers (mean: 66.2 ± 96.9). This difference was statistically significant (p < 0.001) with a strong evidence of correlation (p < 0.001; Spearman’s R: +0.72). ROC curve analysis was performed on CK19 expression index related to HPV positivity. Heterogeneous areas of immunoreactivity varying in percentage value, intensity and/or localization were observed in normal epithelium, both perilesional and distant from the tumor with important differences between HR-HPV+ and HR-HPV− carcinomas. By ICC and flow cytometry, the two analyzed cell lines were both CK19 positive but showed a different level of expression, in particular it should be noted that the UPCI-SCC-154 (HPV+) cell line had a higher expression than UPCI-SCC-131 (HPV−).ConclusionsIn this study we demonstrated, for the first time, strong association between CK19 up-regulation and HR-HPV+ OSCCs/OPSCCs. This test has a good accuracy. We identified ROC curve with a cut-off > 195 for HR-HPV positive results (Sensitivity: 92.3 %; Specificity: 89.3 %). Furthermore, in OSCC/OPSCC, the CK19 test may be useful in identifying HR-HPV infection, the latter being related to HPV E7 potential to disrupt normal cytokeratin expression pattern.

Highlights

  • According to epidemiological studies, a real shift in Oral squamous cell carcinoma (OSCCs)/Oro-pharyngeal squamous cell carcinoma (OPSCCs) aetiology may be one of the main reasons of the recent reported improvements in survival of a specific subgroup of patients, treated with radiotherapy [1]

  • In OSCC/OPSCC, the Cytokeratin 19 (CK19) test may be useful in identifying High Risk-Human Papilloma Virus (HR-HPV) infection, the latter being related to HPV E7 potential to disrupt normal cytokeratin expression pattern

  • Heterogeneous areas of immunoreactivity varying in percentage value, intensity and/or localization were observed in normal epithelium, both perilesional and distant from the tumor

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Summary

Introduction

A real shift in OSCCs/OPSCCs aetiology may be one of the main reasons of the recent reported improvements in survival of a specific subgroup of patients, treated with radiotherapy [1]. As a large group of host specific DNA virus, HPVs are characterized by a considerable broad epithelial cell tropism Considering their potential risk to induce an invasive cancer, almost 45 subtypes, isolated from the low genital tract, have been all along grouped into high- and low- risk HPV types [9]. Meta-analyses have proved that HPV subtypes associated with head and neck squamous cell cancer (HNSCCs) are broadly similar (but not completely identical) with those classically observed in cervical carcinoma [13, 14]. This is likely to reflect a difference in viral life cycles in various and distant mucosal locations, and an associated diversity in mucosal local immune responses [10, 15]. We demonstrate the possible relationship between HR-HPV+ oral/oropharyngeal cancer and the high levels of CK19 expression

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