Targeting epidermal growth factor receptor signalling pathway: A promising therapeutic option for COVID-19.
Aroona RazzaqCyrollah DisomaYuzheng ZhouSiyi TaoZongpeng ChenSixu LiuRong ZhengYongxing ZhangYujie LiaoXuan ChenSijie LiuZijun DongLiangtao XuXu DengShanni LiZanxian XiaPublished in: Reviews in medical virology (2023)
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is continuously producing new variants, necessitating effective therapeutics. Patients are not only confronted by the immediate symptoms of infection but also by the long-term health issues linked to long COVID-19. Activation of epidermal growth factor receptor (EGFR) signalling during SARS-CoV-2 infection promotes virus propagation, mucus hyperproduction, and pulmonary fibrosis, and suppresses the host's antiviral response. Over the long term, EGFR activation in COVID-19, particularly in COVID-19-induced pulmonary fibrosis, may be linked to the development of lung cancer. In this review, we have summarised the significance of EGFR signalling in the context of SARS-CoV-2 infection. We also discussed the targeting of EGFR signalling as a promising strategy for COVID-19 treatment and highlighted erlotinib as a superior option among EGFR inhibitors. Erlotinib effectively blocks EGFR and AAK1, thereby preventing SARS-CoV-2 replication, reducing mucus hyperproduction, TNF-α expression, and enhancing the host's antiviral response. Nevertheless, to evaluate the antiviral efficacy of erlotinib, relevant clinical trials involving an appropriate patient population should be designed.
Keyphrases
- epidermal growth factor receptor
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- tyrosine kinase
- advanced non small cell lung cancer
- pulmonary fibrosis
- clinical trial
- healthcare
- public health
- newly diagnosed
- mental health
- randomized controlled trial
- poor prognosis
- rheumatoid arthritis
- depressive symptoms
- prognostic factors
- oxidative stress
- sleep quality
- genome wide
- endothelial cells
- chronic kidney disease
- open label
- phase ii
- patient reported
- copy number