Targeting cullin-RING ligases for cancer treatment: rationales, advances and therapeutic implications
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  • 作者:Shuju Wu ; Lijie Yu
  • 关键词:NEDDylation ; NEDD8 ; Ubiquitin ; MLN4924 ; mTOR ; DNA damage
  • 刊名:Cytotechnology
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:68
  • 期:1
  • 页码:1-8
  • 全文大小:434 KB
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  • 作者单位:Shuju Wu (1)
    Lijie Yu (1)

    1. School of Life Science and Technology, Harbin Normal University, Harbin, 150025, People’s Republic of China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Biotechnology
    Biomedicine
    Biochemistry
  • 出版者:Springer Netherlands
  • ISSN:1573-0778
文摘
New therapeutic intervention strategies for the treatment of human malignancies are always desired. Approval of bortezomib as a front-line treatment for multiple myeloma highlighted the significance of ubiquitin–proteasome system (UPS) as a promising therapeutic target. However, due to the broad impact of proteasome inhibition, deleterious side effects have been reported with bortezomib treatment. Cullin RING ligases (CRLs)-mediated ubiquitin conjugation process is responsible for the ubiquitin conjugation of 20 % cellular proteins that are designated for degradation through the UPS, most of them are critical proteins involved in cell cycle progression, signaling transduction and apoptosis. Studies have depicted the upstream NEDDylation pathway that controls the CRL activity by regulating the conjugation of an ubiquitin-like-protein NEDD8 to the cullin protein in the complex. A specific pharmaceutical inhibitor of NEDD8 activating enzyme (NAE; E1) MLN4924 was recently developed and has been promoted to Phase I clinical trials for the treatment of several human malignancies. This article summarizes the most recent understanding about the process of NEDD8 conjugation, its relevance for cancer therapy and molecular mechanisms responsible for the potent anti-tumor activity of MLN4924. Keywords NEDDylation NEDD8 Ubiquitin MLN4924 mTOR DNA damage

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