Abstract

Simple SummaryHead and neck cancer (HNC) is the sixth most common cancer, causing almost half a million deaths worldwide every year. The two subtypes of HNC are distinctly associated with smoking/drinking and/or human papillomavirus (HPV) infection. While the incidence of non-viral HNC is decreasing, HPV-positive HNC incidence has dramatically increased in the last few decades. Accumulating evidence from numerous studies shows molecular and clinical differences in mutations, gene expression regulation, treatment responses, and patient survival rates between HPV-positive and HPV-negative HNC. Here, we discuss the current status of HNC research and clinical approaches and suggest unanswered questions and future directions.Head and neck squamous cell carcinoma (HNSCC) is a unique malignancy associated with two distinct risk factors: exposure to typical carcinogens and infection of human papillomavirus (HPV). HPV encodes the potent oncoproteins E6 and E7, which bypass many important oncogenic processes and result in cancer development. In contrast, HPV-negative HNSCC is developed through multiple mutations in diverse oncogenic driver genes. While the risk factors associated with HPV-positive and HPV-negative HNSCCs are discrete, HNSCC patients still show highly complex molecular signatures, immune infiltrations, and treatment responses even within the same anatomical subtypes. Here, we summarize the current understanding of biological mechanisms, treatment approaches, and clinical outcomes in comparison between HPV-positive and -negative HNSCCs.

Highlights

  • Head and neck squamous cell carcinomas (HNSCC) comprise squamous cell carcinoma of the oral cavity, nasal cavity, pharynx, larynx, and tongue

  • A comparison of the oral microbiome between smokers with and without HNSCC have shown that the smoker HNSCC patients have diminished populations of common commensal bacteria involved in carbohydrate metabolism, such as Selenomonas, Veillonella, and Kingella (Table 1) [114]

  • Despite both groups experiencing exposure to the harmful toxins of tobacco, the different oral microbiota is associated with significant different incidence of HNSCC, suggesting that the microbiome plays a role in HNSCC carcinogenesis

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Summary

Introduction

Head and neck squamous cell carcinomas (HNSCC) comprise squamous cell carcinoma of the oral cavity, nasal cavity, pharynx (oropharynx and hypopharynx), larynx, and tongue. These unique gene expression patterns are functionally associated with the significantly higher cell proliferation rate of HPV+ tumor cells compared to HPV− tumor cells These findings imply that HPV+ HNSCC is a cancer type that is distinct from HPV− HNSCC, and requires different treatment strategies. Another study reported that a group of genes in MHC-I and the peptide loading complex are significantly upregulated in HPV+ HNSCC [94] This discrepancy might be caused by the limitations in the standard criteria of tissue sample collections, spatial and temporal heterogeneity, and appropriate technologies to detect MHC-I expression on cancer cell surface from patient tissues. HPV status was shown to correlate to bacterial abundance These differences seen when comparing HPV+ and HPV− HNSCC may be due to interactions between the oral microbiota and behavioral/viral risk factors, such as smoking, alcohol, and HPV infection. Tumor and anatomically matched normal tissue from oral cancer and pre-cancer 129 HNSCC and 254 matched controls 18 oral cavity squamous cell cancer (OCSCC), 8 pre-malignant lesions, 12 control

Major Findings
Clinical Management of HNSCC
Surgery
Multimodality Treatment
Design
Metastatic Disease
Immunotherapy Trials
Conclusions
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