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    Home > Biochemistry News > Biotechnology News > Researchers discover new molecular target for nonalcoholic steatohepatitis

    Researchers discover new molecular target for nonalcoholic steatohepatitis

    • Last Update: 2022-09-09
    • Source: Internet
    • Author: User
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    Figure: IGF2BP2 overexpression leads to liver steatosis (left), inflammation (middle), and hepatocyte apoptosis (right) in mice



    Nonalcoholic steatohepatitis (NASH) is characterized by liver steatosis, inflammation, and damage, and has become one of the leading causes of end-stage liver disease such as hepatocellular carcinoma


    More than two decades ago, the "double hit" theory was proposed to explain the pathogenesis of NASH, in which steatosis is the "first hit" and oxidative stress is the "second hit"


    Researchers from Zhongshan Hospital of Fudan University and the Sixth People's Hospital Affiliated to Shanghai Jiaotong University and other collaborators have jointly identified a novel molecule in the pathogenesis of NASH through three diet- or compound-induced mouse models of chronic liver inflammation and injury mechanism


    In the present study, through unbiased RNA-sequencing analysis and subsequent validation, we identified insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) as a novel N 6 -methyladenosine (m 6 A) modified reader, Significantly increased in NASH mouse liver


    In conclusion, this study confirmed that IGF2BP2 is a key regulator in the occurrence and development of NASH


    article title

    Promotion of nonalcoholic steatohepatitis by RNA N 6-methyladenosine reader IGF2BP2 in mice


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