HDAC8: a multifaceted target for therapeutic interventions

被引:213
作者
Chakrabarti, Alokta [1 ]
Oehme, Ina [2 ]
Witt, Olaf [2 ,3 ]
Oliveira, Guilherme [4 ]
Sippl, Wolfgang [5 ]
Romier, Christophe [6 ]
Pierce, Raymond J. [7 ]
Jung, Manfred [1 ]
机构
[1] Univ Freiburg, Inst Pharmaceut Sci, D-79106 Freiburg, Germany
[2] German Canc Res Ctr, Clin Cooperat Unit Pediat Oncol, Heidelberg, Germany
[3] Univ Heidelberg Hosp, Dept Pediat Oncol Hematol & Immunol, Heidelberg, Germany
[4] Fundacao Oswaldo Cruz, Ctr Pesquisas Rene Rachou, Genom & Computat Biol Grp, Belo Horizonte, MG, Brazil
[5] Univ Halle Wittenberg, Inst Pharm, D-06108 Halle, Germany
[6] Univ Strasbourg UDS, CNRS, INSERM, IGBMC,Dept Biol Struct Integrat, Illkirch Graffenstaden, France
[7] Univ Lille, Inst Pasteur Lille, INSERM U1019, CNRS UMR 8204,CIIL, Lille, France
关键词
histone deacetylases; HDAC8; Cornelia de Lange syndrome; cancer; schistosoma; X-ray crystallography; HISTONE DEACETYLASE 8; UP-REGULATION; SUBSTRATE-SPECIFICITY; BIOLOGICAL EVALUATION; NEGATIVE REGULATION; GENE-TRANSCRIPTION; LYSINE ACETYLATION; EPIGENETIC CONTROL; CRYSTAL-STRUCTURE; PEPTIDE ARRAYS;
D O I
10.1016/j.tips.2015.04.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Histone deacetylase 8 (HDAC8) is a class I histone deacetylase implicated as a therapeutic target in various diseases, including cancer, X-linked intellectual disability, and parasitic infections. It is a structurally well-characterized enzyme that also deacetylates nonhistone proteins. In cancer, HDAC8 is a major 'epigenetic player' that is linked to deregulated expression or interaction with transcription factors critical to tumorigenesis. In the parasite Schistosoma mansoni and in viral infections, HDAC8 is a novel target to subdue infection. The current challenge remains in the development of potent selective inhibitors that would specifically target HDAC8 with fewer adverse effects compared with pan-HDAC inhibitors. Here, we review HDAC8 as a drug target and discuss inhibitors with respect to their structural features and therapeutic interventions.
引用
收藏
页码:481 / 492
页数:12
相关论文
共 98 条
  • [1] HDAC inhibitors in parasitic diseases
    Andrews, Katherine T.
    Haque, Ashraful
    Jones, Malcolm K.
    [J]. IMMUNOLOGY AND CELL BIOLOGY, 2012, 90 (01) : 66 - 77
  • [2] A novel histone deacetylase 8 (HDAC8)-specific inhibitor PCI-34051 induces apoptosis in T-cell lymphomas
    Balasubramanian, S.
    Ramos, J.
    Luo, W.
    Sirisawad, M.
    Verner, E.
    Buggy, J. J.
    [J]. LEUKEMIA, 2008, 22 (05) : 1026 - 1034
  • [3] Chemoproteomics profiling of HDAC inhibitors reveals selective targeting of HDAC complexes
    Bantscheff, Marcus
    Hopf, Carsten
    Savitski, Mikhail M.
    Dittmann, Antje
    Grandi, Paola
    Michon, Anne-Marie
    Schlegl, Judith
    Abraham, Yann
    Becher, Isabelle
    Bergamini, Giovanna
    Boesche, Markus
    Delling, Manja
    Duempelfeld, Birgit
    Eberhard, Dirk
    Huthmacher, Carola
    Mathieson, Toby
    Poeckel, Daniel
    Reader, Valerie
    Strunk, Katja
    Sweetman, Gavain
    Kruse, Ulrich
    Neubauer, Gitte
    Ramsden, Nigel G.
    Drewes, Gerard
    [J]. NATURE BIOTECHNOLOGY, 2011, 29 (03) : 255 - U124
  • [4] The establishment of neuronal properties is controlled by Sox4 and Sox11
    Bergsland, Maria
    Werme, Martin
    Malewicz, Michal
    Perlmann, Thomas
    Muhr, Jonas
    [J]. GENES & DEVELOPMENT, 2006, 20 (24) : 3475 - 3486
  • [5] Drug inhibition of HDAC3 and epigenetic control of differentiation in Apicomplexa parasites
    Bougdour, Alexandre
    Maubon, Daniele
    Baldacci, Patricia
    Ortet, Philippe
    Bastien, Olivier
    Bouillon, Anthony
    Barale, Jean-Christophe
    Pelloux, Herve
    Menard, Robert
    Hakimi, Mohamed-Ali
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (04) : 953 - 966
  • [6] Boyle MI., 2014, Clin Genet
  • [7] Cloning and characterization of a novel human histone deacetylase, HDAC8
    Buggy, JJ
    Sideris, ML
    Mak, P
    Lorimer, DD
    McIntosh, B
    Clark, JM
    [J]. BIOCHEMICAL JOURNAL, 2000, 350 : 199 - 205
  • [8] Carrillo A.K., 2015, BIOORG MED CHEM
  • [9] Pure curcumin increases the expression of SOCS1 and SOCS3 in myeloproliferative neoplasms through suppressing class histone deacetylases
    Chen, Chi-qi
    Yu, Kang
    Yan, Qing-xian
    Xing, Chong-yun
    YiChen
    Yan, Zhuang
    Shi, Yi-fen
    Zhao, Ke-Wen
    Gao, Shen-meng
    [J]. CARCINOGENESIS, 2013, 34 (07) : 1442 - 1449
  • [10] Lysine Acetylation Targets Protein Complexes and Co-Regulates Major Cellular Functions
    Choudhary, Chunaram
    Kumar, Chanchal
    Gnad, Florian
    Nielsen, Michael L.
    Rehman, Michael
    Walther, Tobias C.
    Olsen, Jesper V.
    Mann, Matthias
    [J]. SCIENCE, 2009, 325 (5942) : 834 - 840