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A prolonged exposure of human lung carcinoma epithelial cells to benzo[a]pyrene induces p21-dependent epithelial-to-mesenchymal transition (EMT)-like phenotype

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    SYSNO ASEP0541994
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleA prolonged exposure of human lung carcinoma epithelial cells to benzo[a]pyrene induces p21-dependent epithelial-to-mesenchymal transition (EMT)-like phenotype
    Author(s) Hýžd'alová, M. (CZ)
    Procházková, J. (CZ)
    Strapáčová, S. (CZ)
    Svrzkova, L. (CZ)
    Vacek, Ondřej (BFU-R) ORCID
    Fedr, Radek (BFU-R) ORCID
    Andrysik, Z. (US)
    Hrubá, E. (CZ)
    Líbalová, Helena (UEM-P) RID
    Kléma, J. (CZ)
    Topinka, Jan (UEM-P) RID, ORCID
    Mašek, J. (CZ)
    Souček, Karel (BFU-R) RID, ORCID
    Vondráček, Jan (BFU-R) RID, ORCID
    Machala, M. (CZ)
    Number of authors15
    Article number128126
    Source TitleChemosphere. - : Elsevier - ISSN 0045-6535
    Roč. 263, JAN 2021 (2021)
    Number of pages15 s.
    Publication formOnline - E
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsaryl-hydrocarbon receptor ; polycyclic aromatic-hydrocarbons ; tgf-beta ; a549 cells ; cigarette-smoking
    Subject RIVEA - Cell Biology
    OECD categoryCell biology
    Subject RIV - cooperationInstitute of Experimental Medicine - Cell Biology
    Method of publishingOpen access
    Institutional supportBFU-R - RVO:68081707 ; UEM-P - RVO:68378041
    UT WOS000595802200223
    EID SCOPUS85091122385
    DOI https://doi.org/10.1016/j.chemosphere.2020.128126
    AnnotationDeciphering the role of the aryl hydrocarbon receptor (AhR) in lung cancer cells may help us to better understand the role of toxic AhR ligands in lung carcinogenesis, including cancer progression. We employed human lung carcinoma A549 cells to investigate their fate after continuous two-week exposure to model AhR agonists, genotoxic benzo[a]pyrene (BaP, 1 mu M) and non-genotoxic 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD, 10 nM). While TCDD increased proliferative rate of A549 cells, exposure to BaP decreased cell proliferation and induced epithelial-to-mesenchymal transition (EMT)-like phenotype, which was associated with enhanced cell migration, invasion, and altered cell morphology. Although TCDD also suppressed expression of E-cadherin and activated some genes linked to EMT, it did not induce the EMT-like phenotype. The results of transcriptomic analysis, and the opposite effects of BaP and TCDD on cell proliferation, indicated that a delay in cell cycle progression, together with a slight increase of senescence (when coupled with AhR activation), favors the induction of EMT-like phenotype. The shift towards EMT-like phenotype observed after simultaneous treatment with TCDD and mitomycin C (an inhibitor of cell proliferation) confirmed the hypothesis. Since BaP decreased cell proliferative rate via induction of p21 expression, we generated the A549 cell model with reduced p21 expression and exposed it to BaP for two weeks. The p21 knockdown suppressed the BaP-mediated EMT-like phenotype in A549 cells, thus confirming that a delayed cell cycle progression, together with p21-dependent induction of senescence-related chemokine CCL2, may contribute to induction of EMT-like cell phenotype in lung cells exposed to genotoxic AhR ligands. (C) 2020 Elsevier Ltd. All rights reserved.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2022
    Electronic addresshttps://www.sciencedirect.com/science/article/pii/S0045653520323213?via%3Dihub
Number of the records: 1  

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