國家衛生研究院 NHRI:Item 3990099045/2646
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/2646


    Title: Synergistic activation of the tumor suppressor, HLJ1, by the transcription factors YY1 and activator protein 1
    Authors: Wang, CC;Tsai, MF;Dai, TH;Hong, TM;Chan, WK;Chen, JJW;Yang, PC
    Contributors: National Institute of Cancer Research
    Abstract: HLJ1 is a novel tumor and invasion suppressor that inhibits tumorigenesis and cancer metastasis. However, the mechanism of HLJ1 activation is currently unclear. Here, we identify an enhancer segment in the HLJ1 gene at -2,125 to -1,039 bp upstream of the transcription start site. A 50-bp element between -1,492 and -1,443 bp is the minimal enhancer segment, which includes the activator protein I (AP-1) site (-1,457 to -1,451 bp), an essential regulatory domain that binds the transcriptional factors FosB, JunB and JunD. Chromatin immunoprecipitation assays confirm that these AP-1 family members bind to a specific site in the HLJ1 enhancer segment in vivo. Overexpression of either YY1 at promoter or AP-1 at enhancer results in a 3-fold increase in the transcriptional activity of HLJ1. We propose a novel mechanism whereby expression of the tumor suppressor, HLJ1, is upregulated via enhancer AP-1 binding to promoter YY1 and the coactivator, p300, through DNA bending and multiprotein complex formation. The combined expression of AP-1 and YY1 enhances HLJ1 expression by more than five times and inhibits in vitro cancer cell invasion. Elucidation of the regulatory mechanism of HLJ1 expression may facilitate the development of personalized therapy by inhibiting cancer cell proliferation, angiogenesis, and metastasis.
    Keywords: Oncology
    Date: 2007-05-15
    Relation: Cancer Research. 2007 May;67(10):4816-4826.
    Link to: http://dx.doi.org/10.1158/0008-5472.CAN-07-0504
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0008-5472&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000246778500033
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=34250376736
    Appears in Collections:[Others] Periodical Articles

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