Lycopene Prevents Cell Death in Nrk-52e Cells by Inhibition of High Glucose-Activated Dna Damage and Apoptotic, Autophagic, and Necrotic Pathways

dc.contributor.author Usta, Ayse
dc.contributor.author Yuksek, Veysel
dc.contributor.author Cetin, Sedat
dc.contributor.author Dede, Semiha
dc.date.accessioned 2025-05-10T17:23:35Z
dc.date.available 2025-05-10T17:23:35Z
dc.date.issued 2024
dc.description Cetin, Sedat/0000-0002-6102-8571; Dede, Semiha/0000-0001-5744-6327 en_US
dc.description.abstract This study aims to investigate the effects of lycopene on apoptotic, autophagic, and necrotic pathways, oxidative status, and DNA damage in diabetic nephropathy at the molecular level. The sample of the study includes seven groups: lycopene (L), high glucose (G), high glucose + lycopene (GL), and control (C) groups tested at 12 and 24 h. The expression levels of genes in oxidative, apoptotic, autophagic, and necrotic cell death pathways are determined by reverse transcription-quantitative polymerase chain reaction analysis. The comet assay method is used for the analysis of DNA damage. It is observed that adding lycopene to high glucose for protective purposes reduces the expression of genes related to apoptosis, autophagy, and necrosis, as well as the DNA damage index, compared to cells given high glucose alone. Lycopene can be a safe and effective alternative agent. In this study, where the molecular mechanisms were examined, it was concluded that lycopene, used as an agent of necrosis, autophagy and apoptosis inhibition, had beneficial effects on cells treated with high glucose. image en_US
dc.description.sponsorship Van Yuzuncu Yil University Scientific Research Projects Coordination Unit; [THD-2018-7376] en_US
dc.description.sponsorship The authors are grateful to the Van Yuzuncu Yil University Scientific Research Projects Coordination Unit (THD-2018-7376) for their contributions. en_US
dc.identifier.doi 10.1002/jbt.23678
dc.identifier.issn 1095-6670
dc.identifier.issn 1099-0461
dc.identifier.scopus 2-s2.0-85186891575
dc.identifier.uri https://doi.org/10.1002/jbt.23678
dc.identifier.uri https://hdl.handle.net/20.500.14720/10927
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Cell Death en_US
dc.subject Comet en_US
dc.subject Dna Damage en_US
dc.subject High Glucose en_US
dc.subject Lycopene en_US
dc.title Lycopene Prevents Cell Death in Nrk-52e Cells by Inhibition of High Glucose-Activated Dna Damage and Apoptotic, Autophagic, and Necrotic Pathways en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id Cetin, Sedat/0000-0002-6102-8571
gdc.author.id Dede, Semiha/0000-0001-5744-6327
gdc.author.scopusid 57196420522
gdc.author.scopusid 55736672600
gdc.author.scopusid 23969941600
gdc.author.scopusid 6603709171
gdc.author.wosid Usta, Ayşe/Aai-7545-2021
gdc.author.wosid Dede, Semiha/H-5403-2013
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.description.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
gdc.description.departmenttemp [Usta, Ayse] Van Yuzuncu Yil Univ, Fac Sci, Dept Chem, Van, Turkiye; [Yuksek, Veysel] Van Yuzuncu Yil Univ, Ozalp Reg High Sch, Dept Med Lab Technician, Van, Turkiye; [Cetin, Sedat] Ankara Yildirim Beyazit Univ, Vocat Sch Hlth Serv, Dept Vet Med, Ankara, Turkiye; [Dede, Semiha] Van Yuzuncu Yil Univ, Fac Vet Med, Dept Biochem, Van, Turkiye; [Usta, Ayse] Van Yuzuncu Yil Univ, Fac Sci, Dept Chem, Zeve Campus, TR-65080 Van, Turkiye en_US
gdc.description.issue 3 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.volume 38 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
gdc.identifier.pmid 38444079
gdc.identifier.wos WOS:001178851500001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed

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