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1000 Titel
  • Impact of plastic-related compounds on the gene expression signature of HepG2 cells transfected with CYP3A4
1000 Autor/in
  1. Rosellini, Matteo |
  2. Omer, Ejlal A. |
  3. Schulze, Alicia |
  4. Ali, Nadeen T. |
  5. Boulos, Joelle C. |
  6. Marini, Federico |
  7. Küpper, Jan-Heiner |
  8. Efferth, Thomas |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2023
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2023-12-30
1000 Erschienen in
1000 Quellenangabe
  • 98(2):525-536
1000 Copyrightjahr
  • 2023
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00204-023-03648-4 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10794370/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>The presence of plastic and microplastic within the oceans as well as in marine flora and fauna have caused a multitude of problems that have been the topic of numerous investigations for many years. However, their impact on human health remains largely unknown. Such plastic and microplastic particles have been detected in blood and placenta, underlining their ability to enter the human body. Plastics also contain other compounds, such as plasticizers, antioxidants, or dyes, whose impact on human health is currently being studied. Critical enzymes within the metabolism of endogenous molecules, especially of xenobiotics, are the cytochrome P450 monooxygenases (CYPs). Although their importance in maintaining cellular balance has been confirmed, their interactions with plastics and related products are poorly understood. In this study, the possible relationship between different plastic-related compounds and CYP3A4 as one of the most important CYPs was analyzed using hepatic cells overexpressing this enzyme. Beginning with virtual compound screening and molecular docking of more than 1000 plastic-related compounds, several candidates were identified to interact with CYP3A4. In a second step, RNA-sequencing was used to study in detail the transcriptome-wide gene expression levels affected by the selected compounds. Three candidate molecules ((2,2′-methylenebis(6-<jats:italic>tert</jats:italic>-butyl-4-methylphenol), 1,1-bis(3,5-di-<jats:italic>tert</jats:italic>-butyl-2-hydroxyphenyl)ethane, and 2,2′-methylenebis(6-cyclohexyl-4-methylphenol)) had an excellent binding affinity to CYP3A4 in-silico as well as cytotoxic effects and interactions with several metabolic pathways in-vitro. We identified common pathways influenced by all three selected plastic-related compounds. In particular, the suppression of pathways related to mitosis and ‘DNA-templated DNA replication’ which were confirmed by cell cycle analysis and single-cell gel electrophoresis. Furthermore, several mis-regulated metabolic and inflammation-related pathways were identified, suggesting the induction of hepatotoxicity at different levels. These findings imply that these compounds may cause liver problems subsequently affecting the entire organism.</jats:p>
1000 Sacherschließung
lokal Molecular Docking Simulation [MeSH]
lokal Female [MeSH]
lokal Ecotoxicity
lokal Hepatotoxicity
lokal Plastics/toxicity [MeSH]
lokal Environmental pollution
lokal Humans [MeSH]
lokal In Vitro Systems
lokal Microplastics [MeSH]
lokal Marine pollution
lokal Hep G2 Cells [MeSH]
lokal RNA-sequencing
lokal Cytochrome P-450 Enzyme System/metabolism [MeSH]
lokal Cytochrome P-450 Enzyme System/genetics [MeSH]
lokal Microplastic
lokal Cresols [MeSH]
lokal Cytotoxicity
lokal Transcriptome [MeSH]
lokal Pregnancy [MeSH]
lokal Cytochrome P-450 CYP3A/metabolism [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/Um9zZWxsaW5pLCBNYXR0ZW8=|https://frl.publisso.de/adhoc/uri/T21lciwgRWpsYWwgQS4=|https://frl.publisso.de/adhoc/uri/U2NodWx6ZSwgQWxpY2lh|https://frl.publisso.de/adhoc/uri/QWxpLCBOYWRlZW4gVC4=|https://frl.publisso.de/adhoc/uri/Qm91bG9zLCBKb2VsbGUgQy4=|https://frl.publisso.de/adhoc/uri/TWFyaW5pLCBGZWRlcmljbw==|https://frl.publisso.de/adhoc/uri/S8O8cHBlciwgSmFuLUhlaW5lcg==|https://orcid.org/0000-0002-2637-1681
1000 Hinweis
  • DeepGreen-ID: 9557a059c2a94b62ba04a9cc56a611f4 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Deutsche Forschungsgemeinschaft |
  2. Johannes Gutenberg-Universität Mainz |
1000 Fördernummer
  1. -
  2. -
1000 Förderprogramm
  1. -
  2. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Deutsche Forschungsgemeinschaft |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Johannes Gutenberg-Universität Mainz |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6517484.rdf
1000 Erstellt am 2025-07-05T04:42:03.544+0200
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1000 Zuletzt bearbeitet 2025-08-19T19:10:08.329+0200
1000 Objekt bearb. Tue Aug 19 19:10:08 CEST 2025
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  1. oai:frl.publisso.de:frl:6517484 |
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