SARS-CoV-2 Interaction with Human DNA Methyl Transferase 1: A Potential Risk for Increasing the Incidence of Later Chronic Diseases in the Survived Patients
Currently, the COVID-19 pandemic is the most discussed subject in medical researches worldwide. As the knowledge is expanded about the disease, more hypotheses become created. A recent study on the viral protein interaction map revealed that SARS-CoV-2 open reading frame 8 (ORF8) interacts with huma...
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Published in | International journal of preventive medicine Vol. 13; no. 1 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
01.01.2022
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Online Access | Get full text |
ISSN | 2008-7802 2008-8213 |
DOI | 10.4103/ijpvm.IJPVM_628_20 |
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Abstract | Currently, the COVID-19 pandemic is the most discussed subject in medical researches worldwide. As the knowledge is expanded about the disease, more hypotheses become created. A recent study on the viral protein interaction map revealed that SARS-CoV-2 open reading frame 8 (ORF8) interacts with human DNA methyl transferase1 (DNMT1), an active epigenetic agent in DNA methylation. Moreover, DNMT1 is a contributor to a variety of chronic diseases which could cause some epigenetic dysregulation in infected cells, especially leukocytes, pancreatic beta, and endothelial cells. Regarding the fact that epigenetic alterations have a partial, but not completely reversible phenomena, it raises the question that if this interaction may cause long-term complications such as diabetes, atherosclerosis, cancer, and autoimmune diseases. Accordingly, long follow-up studies on the recovered patients from COVID-19 are recommended. |
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AbstractList | Currently, the COVID-19 pandemic is the most discussed subject in medical researches worldwide. As the knowledge is expanded about the disease, more hypotheses become created. A recent study on the viral protein interaction map revealed that SARS-CoV-2 open reading frame 8 (ORF8) interacts with human DNA methyl transferase1 (DNMT1), an active epigenetic agent in DNA methylation. Moreover, DNMT1 is a contributor to a variety of chronic diseases which could cause some epigenetic dysregulation in infected cells, especially leukocytes, pancreatic beta, and endothelial cells. Regarding the fact that epigenetic alterations have a partial, but not completely reversible phenomena, it raises the question that if this interaction may cause long-term complications such as diabetes, atherosclerosis, cancer, and autoimmune diseases. Accordingly, long follow-up studies on the recovered patients from COVID-19 are recommended. |
Author | Fakhrolmobasheri, Mohammad Zeinalian, Mehrdad Shiravi, Amirabbas |
Author_xml | – sequence: 1 givenname: Mohammad surname: Fakhrolmobasheri fullname: Fakhrolmobasheri, Mohammad organization: Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran – sequence: 2 givenname: Amirabbas surname: Shiravi fullname: Shiravi, Amirabbas organization: Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran – sequence: 3 givenname: Mehrdad surname: Zeinalian fullname: Zeinalian, Mehrdad organization: Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran, Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Diseases, Isfahan University of Medical Sciences, Isfahan, Iran, Iranians Cancer Control Charity Institute (MACSA), Isfahan, Iran |
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Cites_doi | 10.1177/1947601910373794 10.1097/MOL.0000000000000059 10.1038/s41598-017-09536-z 10.1371/journal.pone.0011333 10.1074/jbc.M113.467266 10.1038/srep30053 10.1016/j.taap.2017.03.017 10.2174/1568026619666181120150122 10.1038/s41586-020-2286-9 10.1016/j.clim.2017.12.001 10.1016/j.lfs.2019.03.021 10.1016/j.cmet.2017.01.009 10.1007/s12195-014-0325-z 10.18632/oncotarget.4092 10.18632/oncotarget.10043 |
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