Abstract

Head and neck squamous cell carcinoma (HNSCC) is responsible for a large number of deaths each year. Oral cancer is the most frequent subtype of HNSCC. Historically, oral cancer has been associated with an increase in the consumption of tobacco and alcohol products, seen especially in the Asian subcontinent. It has also been associated with infection by the human papilloma virus (HPV), particularly strain HPV16. Treatment usually involves a multidisciplinary approach of surgery combined with chemotherapy and radiation. The advent of immunotherapy has broadened the scope for treatment. A better immune response to the tumour can also elicit the action of other therapeutic approaches. A heightened immune response, on the other hand, can lead to resistant tumour formation through the process of immunoediting. Molecular profiling of the tumour microenvironment (TME) can provide us with better insight into the mechanism and progression of the disease, ultimately opening up new therapeutic options. High-throughput molecular profiling techniques over the past decade have enabled us to appreciate the heterogeneity of the TME. In this review, we will be describing the clinicopathological role of the immune and genomic landscape in oral cancer. This study will update readers on the several immunological and genetic factors that can play an important function as predictive and prognostic biomarkers in various forms of head and neck cancer, with a special emphasis on oral carcinoma.

Highlights

  • Immunotherapy in the field of oncobiology has been rapidly advancing over the past decade

  • Approaches ranging from oncogene arrays to comparative genome hybridization (CGH), BAC end sequencing and quantitative microsatellite analysis have provided oncology researchers with useful experimental strategies for mapping the genomic markers involved in oncogenesis [15, 16]

  • This review aims to identify the mechanisms involved in the immunosuppression of Head and neck squamous cell carcinoma (HNSCC) biology and to demonstrate a few experimental and therapeutic approaches implemented to surmount the tumour associated immune dysfunction in HNSCC

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Summary

Introduction

Immunotherapy in the field of oncobiology has been rapidly advancing over the past decade. Patients suffering from HNSCC have myriad alterations in their immune cell population They demand a potential therapeutic approach to be highlighted for the proper recovery and lower recurring outcomes. Approaches ranging from oncogene arrays to comparative genome hybridization (CGH), BAC end sequencing and quantitative microsatellite analysis have provided oncology researchers with useful experimental strategies for mapping the genomic markers involved in oncogenesis [15, 16] Modern techniques such as RNA-seq technology have been successfully used to identify global gene expression patterns in tongue squamous cell carcinoma [17]. Critical genetic signatures have been described in detail, which are known to play an important role in the development of oral cancer This would be supportive for the proper developmental immunotherapy approaches

Main text
Role of immune marker expression in tumour progression
T cell
Immune checkpoint molecules
Genomic signatures
Markers located on other loci
Genes involved in oral carcinoma of the tongue and gingivobuccal
Gene expression studies and the role of HPV
Findings
Conclusions

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