Increased susceptibility of SARS-CoV2 infection on oral cancer patients; cause and effects: An hypothesis

Med Hypotheses. 2020 Nov:144:109987. doi: 10.1016/j.mehy.2020.109987. Epub 2020 Jun 9.

Abstract

In 2019, a new coronavirus (SARS CoV2) infecting humans has emerged in Wuhan, China which caused an unprecedented pandemic involving at least 185 countries infecting 2.5 million people till date. This virus is transmitted directly or indirectly through the upper aerodigestive tract. As it is evident from the recent studies that SARS-CoV-2 requires host enzyme Furin to activate receptor binding domain of its S protein and host Angiotensin Convertase Enzyme 2 (ACE2) is required as binding receptor, facilitating the entry of virus into the host cell. Evidence from literature shows that oral cancer tissues as well as paracarcinoma tissue exhibit higher expression of both Furin and ACE2, giving rise to the hypothesis that patients with oral cancer have higher chances of SARS CoV2 infection. It is also hypothesised that there will be increased severity of disease due to facilitated entry of the virus into the cells. Therefore, we suggest oral cancer patients require extra attention during COVID-19 pandemic and re-evaluation of current treatment paradigms in oral oncology is also needed.

MeSH terms

  • Angiotensin-Converting Enzyme 2 / biosynthesis
  • Angiotensin-Converting Enzyme 2 / genetics
  • Angiotensin-Converting Enzyme 2 / physiology*
  • COVID-19 / epidemiology
  • COVID-19 / prevention & control
  • COVID-19 / virology*
  • Disease Susceptibility
  • Furin / genetics
  • Furin / metabolism*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Models, Biological
  • Mouth Neoplasms / genetics
  • Mouth Neoplasms / metabolism
  • Mouth Neoplasms / virology*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Pandemics
  • Protein Binding
  • Receptors, Virus / biosynthesis
  • Receptors, Virus / genetics
  • Receptors, Virus / physiology*
  • SARS-CoV-2 / physiology*
  • Spike Glycoprotein, Coronavirus / metabolism
  • Up-Regulation
  • Virus Internalization*

Substances

  • Neoplasm Proteins
  • Receptors, Virus
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • FURIN protein, human
  • Furin