Low Expression of Nuclear Toll-like Receptor 4 in Laryngeal Papillomas Transforming into Squamous Cell Carcinoma

Author:

Ilmarinen Taru1,Hagström Jaana23,Haglund Caj24,Auvinen Eeva35,Leivo Ilmo6,Pitkäranta Anne1,Aaltonen Leena-Maija1

Affiliation:

1. Department of Otorhinolaryngology–Head and Neck Surgery, Helsinki University Hospital, University of Helsinki, Helsinki, Finland

2. Department of Pathology, Haartman Institute, Helsinki University Hospital, University of Helsinki, Helsinki, Finland

3. Helsinki University Hospital Laboratory, Helsinki University Hospital, University of Helsinki, Helsinki, Finland

4. Department of Surgery, Helsinki University Hospital, University of Helsinki, Helsinki, Finland

5. Department of Virology, Haartman Institute, Helsinki University Hospital, University of Helsinki, Helsinki, Finland

6. Department of Pathology, Turku University Hospital, University of Turku, Turku, Finland

Abstract

Objective The malignant transformation rate of recurrent respiratory papillomatosis (RRP), a disease caused by human papillomavirus (HPV), has varied significantly. Cells of the human immune system express toll-like receptors (TLRs) that recognize particles from viruses and bacteria; TLRs are also present on tumor cells, and down-regulation of TLRs has been shown during the progression of HPV-associated neoplasia. The aim of this study was to determine the malignant transformation rate of laryngeal papillomas (LPs) and analyze the potential of TLR2, TLR4, and TLR9 immunoexpression as indicators of the increased cancer risk. Study Design Retrospective case-control study. Setting Department of Otorhinolaryngology–Head and Neck Surgery, Helsinki University Hospital, University of Helsinki, Helsinki, Finland. Subjects and Methods We reviewed all patients with RRP treated for LPs between 1975 and 2011. Data from the Finnish Cancer Registry confirmed the number of patients diagnosed with laryngeal squamous cell carcinoma (LSCC). Laryngeal tissue specimens from patients developing LSCC were subjected to TLR2, TLR4, and TLR9 immunohistochemistry. Nine patients with RRP without malignant transformation and 19 patients with LSCC without a pre-existing LP served as controls. Results Nine of 324 patients (2.8%) with RRP developed LSCC. The intensity of nuclear staining of TLR4 was significantly lower in LPs transforming into LSCC than in LPs without malignant transformation. The expression of cytoplasmic TLR4 in LSCC correlated with tumor grade and T stage. Cytoplasmic TLR9 expression was significantly lower in LPs than in LSCC. Conclusion The expression of TLR4 may serve as a predictive marker of malignant transformation in LPs. High immunoexpression of cytoplasmic TLR4 in LSCC was associated with a more aggressive disease.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Surgery

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