IGSF3 tissue expression in squamous cell carcinoma of the oropharynx: a novel tool for prognosis assessment in HPV‐related and HPV‐unrelated disease

Author:

Sjöblom Anni12ORCID,Jouhi Lauri3,Laakkonen Pirjo4,Randén‐Brady Reija1,Tarkkanen Jussi1,Haglund Caj45,Mattila Petri3,Carpén Timo12,Hagström Jaana146,Mäkitie Antti237

Affiliation:

1. Department of Pathology University of Helsinki and Helsinki University Hospital Helsinki Finland

2. Research Program in Systems Oncology, Faculty of Medicine University of Helsinki Helsinki Finland

3. Department of Otorhinolaryngology—Head and Neck Surgery University of Helsinki and Helsinki University Hospital Helsinki Finland

4. Translational Cancer Medicine Research Program, Faculty of Medicine University of Helsinki Helsinki Finland

5. Department of Surgery University of Helsinki and Helsinki University Hospital Helsinki Finland

6. Department of Oral Pathology and Oral Radiology University of Turku Turku Finland

7. Division of Ear, Nose and Throat Diseases, Department of Clinical Sciences, Intervention and Technology Karolinska Institutet and Karolinska Hospital Stockholm Sweden

Abstract

Biomarkers are not broadly used in the management of head and neck cancers (HNCs). Biomarkers have been beneficial in the management of other cancers, however, not in HNCs. Therefore, we observed the immunopositivity of a novel biomarker called immunoglobulin superfamily member 3 (IGSF3) in tumor tissues in HPV‐related and HPV‐unrelated OPSCC. Two patient cohorts (C1 and C2) from separate time periods were available for this study (total N = 282). Both consisted of OPSCC patients treated at the Helsinki University Hospital (HUS, Helsinki, Finland) during 2000–2016. For HPV determination, HPV mRNA in situ hybridization was used. Immunohistochemistry was used to assess IGSF3 immunopositivity in cancer tissues. Overall survival (OS) was used as endpoint in the statistical analysis. In C1, stronger immunopositivity of IGSF3 in tumor‐infiltrating lymphocytes (TILs) correlated with favorable OS (p = 0.005). Stronger IGSF3 immunopositivity in tumor cells (TCs) was associated with HPV negativity (p = 0.017). Stronger IGSF3 immunopositivity in TILs correlated with HPV positivity (p < 0.001). Elevated IGSF3 immunopositivity in TILs associates with HPV‐related tumors and may signify favorable prognosis. The immunopositivity of IGSF3 differs between HPV‐related and HPV‐unrelated OPSCC.

Funder

Ida Montinin Säätiö

Suomen Hammaslääkäriseura Apollonia

Korvatautien Tutkimussäätiö

Minerva Foundation

Finnish Cancer Institute

Publisher

Wiley

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