Number of the records: 1  

The role of m6A and m6Am RNA modifications in the pathogenesis of diabetes mellitus

  1. 1.
    0573796 - FGÚ 2024 RIV CH eng J - Journal Article
    Benák, Daniel - Benáková, Štěpánka - Plecitá-Hlavatá, Lydie - Hlaváčková, Markéta
    The role of m6A and m6Am RNA modifications in the pathogenesis of diabetes mellitus.
    Frontiers in Endocrinology. Roč. 14, July (2023), č. článku 1223583. ISSN 1664-2392. E-ISSN 1664-2392
    R&D Projects: GA ČR(CZ) GJ19-04790Y; GA MŠMT(CZ) LX22NPO5104; GA ČR(CZ) GA22-11439S
    Institutional support: RVO:67985823
    Keywords : type 2 diabetes mellitus * T2DM * diabetes * RNA * epigenetics * epitranscriptomics * m6A * m6Am
    OECD category: Physiology (including cytology)
    Impact factor: 5.2, year: 2022
    Method of publishing: Open access
    https://doi.org/10.3389/fendo.2023.1223583

    The rapidly developing research field of epitranscriptomics has recently emerged into the spotlight of researchers due to its vast regulatory effects on gene expression and thereby cellular physiology and pathophysiology. N6-methyladenosine (m6A) and N6,2’-O-dimethyladenosine (m6Am) are among the most prevalent and well-characterized modified nucleosides in eukaryotic RNA. Both of these modifications are dynamically regulated by a complex set of epitranscriptomic regulators called writers, readers, and erasers. Altered levels of m6A and also several regulatory proteins were already associated with diabetic tissues. This review summarizes the current knowledge and gaps about m6A and m6Am modifications and their respective regulators in the pathophysiology of diabetes mellitus. It focuses mainly on the more prevalent type 2 diabetes mellitus (T2DM) and its treatment by metformin, the first-line antidiabetic agent. A better understanding of epitranscriptomic modifications in this highly prevalent disease deserves further investigation and might reveal clinically relevant discoveries in the future.
    Permanent Link: https://hdl.handle.net/11104/0344151

     
    FileDownloadSizeCommentaryVersionAccess
    23_0062_0573796.pdf12 MBPublisher’s postprintopen-access
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.