| Literature DB >> 32910699 |
Amit Verma1, Amitava Adhikary2, Gayle Woloschak3, Bilikere S Dwarakanath4, Rao V L Papineni5.
Abstract
COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a pandemic disease and is the major cause of deaths worldwide. The clinical complexities (inflammation, cytokine storm, and multi-organ dysfunction) associated with COVID-19 poses constraints to effective management of critically ill COVID-19 patients. Low dose radiation therapy (LDRT) has been evaluated as a potential therapeutic modality for COVID-19 pneumonia. However, due to heterogeneity in disease manifestation and inter-individual variations, effective planning for LDRT is limited for this large-scale event. 2-deoxy-D-glucose (2-DG) has emerged as a polypharmacological agent for COVID-19 treatment due to its effects on the glycolytic pathway, anti-inflammatory action, and interaction with viral proteins. We suggest that 2-DG will be a potential adjuvant to enhance the efficacy of LDRT in the treatment of COVID-19 pneumonia. Withal, azido analog of 2-DG, 2-azido-2-DG can produce rapid catastrophic oxidative stress and quell the cytokine storm in critically ill COVID-19 patients.Entities:
Keywords: 2-azido-2-deoxy-D-glucose; 2-deoxy-D-glucose (2-DG); COVID-19; Low dose radiation therapy (LDRT); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
Mesh:
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Year: 2020 PMID: 32910699 DOI: 10.1080/09553002.2020.1818865
Source DB: PubMed Journal: Int J Radiat Biol ISSN: 0955-3002 Impact factor: 2.694