Impact of Epstein Barr Virus Infection on Treatment Opportunities in Patients with Nasopharyngeal Cancer

• Published in: Cancers 2023-03, Vol.15 (5), p.1626
• Main Authors: Perri, Francesco, Sabbatino, Francesco, Ottaiano, Alessandro, Fusco, Roberta, Caraglia, Michele, Cascella, Marco, Longo, Francesco, Rega, Rosalia Anna, Salzano, Giovanni, Pontone, Monica, Marciano, Maria Luisa, Piccirillo, Arianna, Montano, Massimo, Fasano, Morena, Ciardiello, Fortunato, Della Vittoria Scarpati, Giuseppina, Ionna, Franco
• Format: Article
• Language: English
• Subjects: Adoptive immunotherapy; Antigen (tumor-associated); Antigens; Apoptosis; Cancer; Carcinogenesis; Care and treatment; Cell cycle; Cell division; Complications and side effects; Cytokines; Cytotoxicity; Dendritic cells; Development and progression; Epithelial cells; Epstein-Barr virus; Epstein-Barr virus diseases; Evaluation; Genomes; Genotype & phenotype; Immune checkpoint inhibitors; Immune response; Immunotherapy; Infections; Kinases; Latency; Lymphocytes; Malignancy; Molecular modelling; Mutation; Nasopharyngeal cancer; Nasopharyngeal carcinoma; Patient outcomes; Proteins; Review; Risk factors; Tumor microenvironment; Tumors; Viruses
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers15051626

Chemical, physical, and infectious agents may induce carcinogenesis, and in the latter case, viruses are involved in most cases. The occurrence of virus-induced carcinogenesis is a complex process caused by an interaction across multiple genes, mainly depending by the type of the virus. Molecular mechanisms at the basis of viral carcinogenesis, mainly suggest the involvement of a dysregulation of the cell cycle. Among the virus-inducing carcinogenesis, Epstein Barr Virus (EBV) plays a major role in the development of both hematological and oncological malignancies and importantly, several lines of evidence demonstrated that nasopharyngeal carcinoma (NPC) is consistently associated with EBV infection. Cancerogenesis in NPC may be induced by the activation of different EBV "oncoproteins" which are produced during the so called "latency phase" of EBV in the host cells. Moreover, EBV presence in NPC does affect the tumor microenvironment (TME) leading to a strongly immunosuppressed status. Translational implications of the above-mentioned statements are that EBV-infected NPC cells can express proteins potentially recognized by immune cells in order to elicit a host immune response (tumor associated antigens). Three immunotherapeutic approaches have been implemented for the treatment of NPC including active, adoptive immunotherapy, and modulation of immune regulatory molecules by use of the so-called checkpoint inhibitors. In this review, we will highlight the role of EBV infection in NPC development and analyze its possible implications on therapy strategies.