The design and development of covalent protein-protein interaction inhibitors for cancer treatment

被引:71
|
作者
Cheng, Sha-Sha [1 ]
Yang, Guan-Jun [1 ]
Wang, Wanhe [2 ,3 ]
Leung, Chung-Hang [1 ]
Ma, Dik-Lung [2 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Hong Kong Baptist Univ, Dept Chem, Kowloon, Hong Kong 999077, Peoples R China
[3] Northwestern Polytech Univ, Inst Med Res, Xian 710072, Peoples R China
基金
中国国家自然科学基金;
关键词
Protein-protein interaction; Covalent inhibitors; Cancer therapy; SMALL-MOLECULE INHIBITORS; DRUG DISCOVERY; SELECTIVE-INHIBITION; BINDING-SITES; POTENT; IDENTIFICATION; REACTIVITY; CYSTEINE; MECHANISM; DATABASE;
D O I
10.1186/s13045-020-00850-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Protein-protein interactions (PPIs) are central to a variety of biological processes, and their dysfunction is implicated in the pathogenesis of a range of human diseases, including cancer. Hence, the inhibition of PPIs has attracted significant attention in drug discovery. Covalent inhibitors have been reported to achieve high efficiency through forming covalent bonds with cysteine or other nucleophilic residues in the target protein. Evidence suggests that there is a reduced risk for the development of drug resistance against covalent drugs, which is a major challenge in areas such as oncology and infectious diseases. Recent improvements in structural biology and chemical reactivity have enabled the design and development of potent and selective covalent PPI inhibitors. In this review, we will highlight the design and development of therapeutic agents targeting PPIs for cancer therapy.
引用
收藏
页数:14
相关论文
共 50 条
  • [31] Protein-Protein Interaction: Prediction, Design, and Modulation
    Zhang Chang-Sheng
    Lai Lu-Hua
    ACTA PHYSICO-CHIMICA SINICA, 2012, 28 (10) : 2363 - 2380
  • [32] Electrostatic Similarities between Protein and Small Molecule Ligands Facilitate the Design of Protein-Protein Interaction Inhibitors
    Voet, Arnout
    Berenger, Francois
    Zhang, Kam Y. J.
    PLOS ONE, 2013, 8 (10):
  • [33] Structure-based design of a protein-protein interaction inhibitor, ABT-263, for the treatment of cancer
    Wendt, Michael D.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2009, 238
  • [34] Development of analytical techniques for protein-protein interaction
    Sun Yu
    Jia Ling-Yun
    Ren Jun
    CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2007, 35 (05) : 760 - 766
  • [35] Recent advancements in the discovery of protein-protein interaction inhibitors of replication protein A
    Patrone, James D.
    Waterson, Alex G.
    Fesik, Stephen W.
    MEDCHEMCOMM, 2017, 8 (02) : 259 - 267
  • [36] Discovery of YAP-TEAD protein-protein interaction (PPI) inhibitors for cancer therapy
    Soude, Anne
    Barth, Martine
    Bocart, Stephanie
    Thoreau, Frederic
    Masson, Philippe
    Braccini, Isabelle
    Montalbetti, Christian
    Brogue, Pierre
    Fromond, Claudia
    CANCER RESEARCH, 2016, 76
  • [37] Protein-protein interaction network of prostate cancer
    Ghayyur, Omaid
    Islam, Muhammad Arshad
    PROCEEDINGS OF 2019 16TH INTERNATIONAL BHURBAN CONFERENCE ON APPLIED SCIENCES AND TECHNOLOGY (IBCAST), 2019, : 278 - 282
  • [38] Recent progress in the development of protein-protein interaction inhibitors targeting androgen receptor-coactivator binding in prostate cancer
    Biron, Eric
    Bedard, Francois
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2016, 161 : 36 - 44
  • [39] Covalent Inhibitors of Protein-Protein Interactions Targeting Lysine, Tyrosine, or Histidine Residues
    Gambini, Luca
    Baggio, Carlo
    Udompholkul, Parima
    Jossart, Jennifer
    Salem, Ahmed F.
    Perry, J. Jefferson P.
    Pellecchia, Maurizio
    JOURNAL OF MEDICINAL CHEMISTRY, 2019, 62 (11) : 5616 - 5627
  • [40] Machine Learning Models to Predict Protein-Protein Interaction Inhibitors
    Diaz-Eufracio, Barbara, I
    Medina-Franco, Jose L.
    MOLECULES, 2022, 27 (22):