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1000 Titel
  • Changes in gene expression patterns in postmortem human myocardial infarction
1000 Autor/in
  1. Wilmes, Verena |
  2. Lux, Constantin |
  3. Niess, Constanze |
  4. Gradhand, Elise |
  5. Verhoff, Marcel A. |
  6. Kauferstein, Silke |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-05-12
1000 Erschienen in
1000 Quellenangabe
  • 134(5):1753-1763
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00414-020-02311-2 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7417407/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • In murine models, the expression of inducible nitric oxide synthase (iNOS) in myocardial infarction (MI) has been reported to be the result of tissue injury and inflammation. In the present study, mRNA expression of iNOS, hypoxia-inducible factor-1α (HIF-1α), and vascular endothelial growth factor (VEGF) was investigated in postmortem human infarction hearts. Since HIF-1α is the inducible subunit of the transcription factor HIF-1, which regulates transcription of iNOS and VEGF, the interrelation between the three genes was observed, to examine the molecular processes during the emergence of MI. iNOS and VEGF mRNAs were found to be significantly upregulated in the affected regions of MI hearts in comparison to healthy controls. Upregulation of HIF-1α was also present but not significant. Correlation analysis of the three genes indicated a stronger and significant correlation between HIF-1α and iNOS mRNAs than between HIF-1α and VEGF. The results of the study revealed differences in the expression patterns of HIF-1 downstream targets. The stronger transcription of iNOS by HIF-1 in the affected regions of MI hearts may represent a pathological process, since no correlation of iNOS and HIF-1α mRNA was found in non-affected areas of MI hearts. Oxidative stress is considered to cause molecular changes in MI, leading to increased iNOS expression. Therefore, it may also represent a forensic marker for detection of early changes in heart tissue.
1000 Sacherschließung
lokal Female [MeSH]
lokal Inducible nitric oxide synthase (iNOS)
lokal Hypoxia
lokal Transcription regulation
lokal Humans [MeSH]
lokal Myocardial Infarction/pathology [MeSH]
lokal RNA, Messenger/genetics [MeSH]
lokal Gene Expression [MeSH]
lokal Original Article
lokal Vascular Endothelial Growth Factor A/metabolism [MeSH]
lokal Postmortem Changes [MeSH]
lokal Male [MeSH]
lokal Nitric Oxide Synthase Type II/metabolism [MeSH]
lokal Hypoxia-inducible factor-1α (HIF-1α)
lokal Up-Regulation/genetics [MeSH]
lokal Hypoxia-Inducible Factor 1, alpha Subunit/metabolism [MeSH]
lokal Vascular endothelial growth factor (VEGF)
lokal Myocardial infarction (MI)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/V2lsbWVzLCBWZXJlbmE=|https://frl.publisso.de/adhoc/uri/THV4LCBDb25zdGFudGlu|https://frl.publisso.de/adhoc/uri/Tmllc3MsIENvbnN0YW56ZQ==|https://frl.publisso.de/adhoc/uri/R3JhZGhhbmQsIEVsaXNl|https://frl.publisso.de/adhoc/uri/VmVyaG9mZiwgTWFyY2VsIEEu|https://frl.publisso.de/adhoc/uri/S2F1ZmVyc3RlaW4sIFNpbGtl
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1000 Erstellt am 2023-11-18T00:10:35.170+0100
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