Insight into Oncogenic Viral Pathways as Drivers of Viral Cancers: Implication for Effective Therapy

Curr Oncol. 2023 Feb 5;30(2):1924-1944. doi: 10.3390/curroncol30020150.

Abstract

As per a recent study conducted by the WHO, 15.4% of all cancers are caused by infectious agents of various categories, and more than 10% of them are attributed to viruses. The emergence of COVID-19 has once again diverted the scientific community's attention toward viral diseases. Some researchers have postulated that SARS-CoV-2 will add its name to the growing list of oncogenic viruses in the long run. However, owing to the complexities in carcinogenesis of viral origin, researchers across the world are struggling to identify the common thread that runs across different oncogenic viruses. Classical pathways of viral oncogenesis have identified oncogenic mediators in oncogenic viruses, but these mediators have been reported to act on diverse cellular and multiple omics pathways. In addition to viral mediators of carcinogenesis, researchers have identified various host factors responsible for viral carcinogenesis. Henceforth owing to viral and host complexities in viral carcinogenesis, a singular mechanistic pathway remains yet to be established; hence there is an urgent need to integrate concepts from system biology, cancer microenvironment, evolutionary perspective, and thermodynamics to understand the role of viruses as drivers of cancer. In the present manuscript, we provide a holistic view of the pathogenic pathways involved in viral oncogenesis with special emphasis on alteration in the tumor microenvironment, genomic alteration, biological entropy, evolutionary selection, and host determinants involved in the pathogenesis of viral tumor genesis. These concepts can provide important insight into viral cancers, which can have an important implication for developing novel, effective, and personalized therapeutic options for treating viral cancers.

Keywords: bio-thermodynamics; cancer; genome; metabolic; oncogenes; pathogenesis; transition; virus.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19*
  • Carcinogenesis
  • Genomics
  • Humans
  • Neoplasms* / genetics
  • Oncogenic Viruses
  • SARS-CoV-2
  • Tumor Microenvironment

Grants and funding

The study was financially supported by the Department of Public Health, College of Health Sciences, Saudi Electronic University Public Health Saudi Arabia, Riyadh, 11673 Riyadh, Saudi Arabia.