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Is haem the real target of COVID-19?

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DOI: 10.1016/j.pdpdt.2021.102381

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DGCR8-DROSHA; Haem; HO-1; miRNA; PDT; SARS-CoV-2; COVID-19

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Despite the launch of vaccination campaigns, the emergence of new variants of the COVID-19 virus has raised concerns, emphasizing the importance of finding ways to prevent or reduce its virulence and pathogenicity. The virus interacts with hemoglobin, inducing hemolysis and potentially disrupting miRNA processing, which could impede the antiviral response. Understanding these mechanisms is crucial in effectively combating the ongoing pandemic.
Although a vaccination campaign has been launched in many countries, the COVID-19 pandemic is not under control. The main concern is the emergence of new variants of SARS-CoV-2; therefore, it is important to find approaches to prevent or reduce the virulence and pathogenicity of the virus. Currently, the mechanism of action of SARS-CoV-2 is not fully understood. Considering the clinical effects that occur during the disease, attacking the human respiratory and hematopoietic systems, and the changes in biochemical parameters (including de-creases in haemoglobin [Hb] levels and increases in serum ferritin), it is clear that iron metabolism is involved. SARS-CoV-2 induces haemolysis and interacts with Hb molecules via ACE2, CD147, CD26, and other receptors located on erythrocytes and/or blood cell precursors that produce dysfunctional Hb. A molecular docking study has reported a potential link between the virus and the beta chain of haemoglobin and attack on haem. Considering that haem is involved in miRNA processing by binding to the DGCR8-DROSHA complex, we hypothesised that the virus may check this mechanism and thwart the antiviral response.

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