Počet záznamů: 1  

Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism

  1. 1.
    SYSNO ASEP0533049
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevNuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
    Tvůrce(i) Smolková, Katarína (FGU-C) RID, ORCID, SAI
    Mikó, E. (HU)
    Kovács, T. (HU)
    Leguina-Ruzzi, Alberto A. (FGU-C) RID, ORCID
    Sipos, A. (HU)
    Bai, P. (HU)
    Zdroj.dok.Antioxidants & Redox Signaling. - : Mary Ann Liebert - ISSN 1523-0864
    Roč. 33, č. 13 (2020), s. 966-997
    Poč.str.32 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovaNRF2 ; cancer ; cancer metabolism ; reactive species
    Vědní obor RIVCE - Biochemie
    Obor OECDBiochemistry and molecular biology
    CEPNV19-01-00101 GA MZd - Ministerstvo zdravotnictví
    Způsob publikováníOpen access
    Institucionální podporaFGU-C - RVO:67985823
    UT WOS000525301800001
    EID SCOPUS85086841484
    DOI https://doi.org/10.1089/ars.2020.8024
    AnotaceRecent Advances: The noncanonical activation of NRF2 was recently discovered, and members of this pathway are involved in carcinogenesis. Further, cancer-related changes (e.g., metabolic flexibility) that support cancer progression were found to be redox- and NRF2 dependent.
    Critical Issues: NRF2 undergoes Janus-faced behavior in cancers. The pro- or antineoplastic effects of NRF2 are context dependent and essentially based on the specific molecular characteristics of the cancer in question. Therefore, systematic investigation of NRF2 signaling is necessary to clarify its role in cancer etiology. The biggest challenge in the NRF2 field is to determine which cancers can be targeted for better clinical outcomes. Further, large-scale genomic and transcriptomic studies are missing to correlate the clinical outcome with the activity of the NRF2 system.
    Future Directions: To exploit NRF2 in a clinical setting in the future, the druggable members of the NRF2 pathway should be identified. In addition, it will be important to study how the modulation of the NRF2 system interferes with cytostatic drugs and their combinations.
    PracovištěFyziologický ústav
    KontaktLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Rok sběru2021
    Elektronická adresahttps://www.liebertpub.com/doi/10.1089/ars.2020.8024
Počet záznamů: 1  

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