Investigation of CYP2E1 and Caspase-3 Gene Expressions in COVID-19 patients

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  • SDG 3 · Sağlık ve Kaliteli Yaşam

Özet

Background: COVID-19 pandemic spread around the world like an infectious disease that presents waved effects on patients. Some patients needed ICU and respiratory support. Some patients only had flu-like symptoms. Cytokine storm and elevated ROS were serious problems for treatment. Apoptotic genes and CYP Family are part of these mechanisms. Aim: In this study, our aim was to examine the gene expression CYP2E1 and Caspase-3 in patients with COVID-19 infection. Method: 60 COVID-19(+) patients (ICU and non-ICU patients) and 30 healthy volunteers were enrolled to study. To measure the level of gene expression qPCR was used. The 2-ΔΔCt method was utilized to analyze gene expression. Results: The expression of CYP2E1 and Caspase-3 genes showed a significant discrepancy between patients and healthy individuals. Caspase-3 expression increased (p=0,0041) but CYP2E1 expression decreased (p=0,0214) in COVID-19 patients compared to healthy individuals. Both levels of gene expression were lower in patients with affected lungs than patients with unaffected lungs (p<0,05). Laboratory findings including d-Dimer, LDH, platelet count, lymphocyte count were related to both gene expressions (p<0,05). We found no correlation between CYP2E1 and Caspase-3 expressions. Conclusion: The expression of Caspase-3 demonstrated apoptotic situations of patients but was not related to the CYP2E1 expression level. CYP2E1 gene expression is an important actor to metabolize endogens and xenobiotics however, COVID-19 patients demonstrated decreased CYP2E1 expression. CYP2E1 and Caspase-3 gene expression levels may be used as a diagnostic tool for COVID-19 patients.

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Tam Kayıt
AlanDeğerDil
dc.contributor.authorKarabulut Uzuncakmak, S.
dc.contributor.authorDirican, E.
dc.contributor.authorNaldan, M.E.
dc.contributor.authorKesmez Can, F.
dc.contributor.authorHalıcı, Z.
dc.date.accessioned2026-10-29T19:10:47.411939558Z
dc.date.available2026-10-29T19:10:47.411939558Z
dc.date.issued2022
dc.description.abstractBackground: COVID-19 pandemic spread around the world like an infectious disease that presents waved effects on patients. Some patients needed ICU and respiratory support. Some patients only had flu-like symptoms. Cytokine storm and elevated ROS were serious problems for treatment. Apoptotic genes and CYP Family are part of these mechanisms. Aim: In this study, our aim was to examine the gene expression CYP2E1 and Caspase-3 in patients with COVID-19 infection. Method: 60 COVID-19(+) patients (ICU and non-ICU patients) and 30 healthy volunteers were enrolled to study. To measure the level of gene expression qPCR was used. The 2-ΔΔCt method was utilized to analyze gene expression. Results: The expression of CYP2E1 and Caspase-3 genes showed a significant discrepancy between patients and healthy individuals. Caspase-3 expression increased (p=0,0041) but CYP2E1 expression decreased (p=0,0214) in COVID-19 patients compared to healthy individuals. Both levels of gene expression were lower in patients with affected lungs than patients with unaffected lungs (p<0,05). Laboratory findings including d-Dimer, LDH, platelet count, lymphocyte count were related to both gene expressions (p<0,05). We found no correlation between CYP2E1 and Caspase-3 expressions. Conclusion: The expression of Caspase-3 demonstrated apoptotic situations of patients but was not related to the CYP2E1 expression level. CYP2E1 gene expression is an important actor to metabolize endogens and xenobiotics however, COVID-19 patients demonstrated decreased CYP2E1 expression. CYP2E1 and Caspase-3 gene expression levels may be used as a diagnostic tool for COVID-19 patients.
dc.identifier.articlenumber101497
dc.identifier.doi10.1016/j.genrep.2022.101497
dc.identifier.eissn2452-0144
dc.identifier.issn2452-0144
dc.identifier.pmcidPMC8760173
dc.identifier.pmid35071821
dc.identifier.scopus2-s2.0-85122962408
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/13321
dc.identifier.volume26
dc.identifier.wosWOS:000745658300003
dc.language.isoen
dc.publisherElsevier Inc.
dc.relation.ispartofGene Reports
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCaspase-3
dc.subjectCCYP2E1
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subject.classificationGenetics & Heredity
dc.subject.otheralanine aminotransferase
dc.subject.otheralbumin
dc.subject.otheraspartate aminotransferase
dc.subject.otherbilirubin
dc.subject.otherC reactive protein
dc.subject.othercaspase 3
dc.subject.othercreatinine
dc.subject.othercytochrome P450
dc.subject.othercytochrome P450 2E1
dc.subject.otherD dimer
dc.subject.otherfibrinogen
dc.subject.otherhemoglobin
dc.subject.otherlactate dehydrogenase
dc.subject.otherprocalcitonin
dc.subject.otheradult
dc.subject.otheralanine aminotransferase blood level
dc.subject.otheralbumin blood level
dc.subject.otherArticle
dc.subject.otheraspartate aminotransferase blood level
dc.subject.otherbilirubin blood level
dc.subject.othercomparative study
dc.subject.othercontrolled study
dc.subject.othercoronavirus disease 2019
dc.subject.othercreatinine blood level
dc.subject.otherfemale
dc.subject.otherfibrinogen blood level
dc.subject.othergene expression
dc.subject.otherhematocrit
dc.subject.otherhemoglobin blood level
dc.subject.otherhuman
dc.subject.otherlactate dehydrogenase blood level
dc.subject.otherlymphocyte count
dc.subject.othermajor clinical study
dc.subject.othermale
dc.subject.othermiddle aged
dc.subject.otherneutrophil
dc.subject.otherplatelet count
dc.subject.otherprotein expression
dc.subject.otherSevere acute respiratory syndrome coronavirus 2
dc.subject.otherurea nitrogen blood level
dc.titleInvestigation of CYP2E1 and Caspase-3 Gene Expressions in COVID-19 patients
dc.typeArticle
rdl.citation.openalex7
rdl.citation.scopus8
rdl.citation.wos5
rdl.departmentHealth Services Vocational School, Bayburt University, Bayburt 69000, Turkey
rdl.departmentDepartment of Anesthesia, Regional Education and Research Hospital, Erzurum 25240, Turkey
rdl.departmentFaculty of Medicine, Department of Infectious and Clinical Microbiology Diseases, Atatürk University, Erzurum 25240, Turkey
rdl.departmentFaculty of Medicine, Department of Pharmacology, Atatürk University, Erzurum 25240, Turkey
rdl.departmentClinical Research, Development and Design Application and Research Center, Ataturk University, 25240 Erzurum, Turkey
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.scopus.quartileQ4
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexEmerging Sources Citation Index (ESCI)