Genetic and epigenetic concept of SARS-CoV-2 targets in different renal cancer subtypes


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Akın D. F., SAĞKAN R. I.

Türk Biyokimya Dergisi, cilt.46, sa.2, ss.145-155, 2021 (SCI-Expanded, Scopus, TRDizin) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 46 Sayı: 2
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1515/tjb-2020-0233
  • Dergi Adı: Türk Biyokimya Dergisi
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, EMBASE, Food Science & Technology Abstracts, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.145-155
  • Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
  • Uşak Üniversitesi Adresli: Evet

Özet

bjectives: Recent advances in defining the genetic landscape of has shown the host cell- SARS-CoV-2 inte raction via ACE2 protein and the presence of at least three additional virus invasion genes including TMPRSS2, FURIN, CD147/BSG. In current study, we investigated the mutation and m-RNA expression patterns of target genes by evalua ting the associations between genetic and epigenetic mec hanisms in the target genes and susceptibility of SARS-CoV 2 infection of renal cancer subtypes. Methods: We investigated the mutation and m-RNA exp ression patterns of our target genes. The promoter methy lation profiles of target genes were tested in the UALCAN database. Results: The total rate of carrying genetic anomaly in the target genes including was 1.6% and seven mutations, one of which had a pathogenic feature, were detected. The expression analysis results in renal cancer groups showed that while the KIRC and KIRP patients had a lower level of TMPRSS2 than the healthy control, their ACE2 level was high. KICH patients had a higher level of CD147/BSG expression than the healthy group. The promoter methylation levels of ACE2 in KIRC and KIRP were reduced. Conclusions: We concluded that renal cancer patients may be more sensitive to SARS-CoV-2 infection, which may worsen the prognosis.