HDAC8: a multifaceted target for therapeutic interventions

被引:222
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 [J].
Andrews, Katherine T. ;
Haque, Ashraful ;
Jones, Malcolm K. .
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 [J].
Balasubramanian, S. ;
Ramos, J. ;
Luo, W. ;
Sirisawad, M. ;
Verner, E. ;
Buggy, J. J. .
LEUKEMIA, 2008, 22 (05) :1026-1034
[3]   Chemoproteomics profiling of HDAC inhibitors reveals selective targeting of HDAC complexes [J].
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 .
NATURE BIOTECHNOLOGY, 2011, 29 (03) :255-U124
[4]   The establishment of neuronal properties is controlled by Sox4 and Sox11 [J].
Bergsland, Maria ;
Werme, Martin ;
Malewicz, Michal ;
Perlmann, Thomas ;
Muhr, Jonas .
GENES & DEVELOPMENT, 2006, 20 (24) :3475-3486
[5]   Drug inhibition of HDAC3 and epigenetic control of differentiation in Apicomplexa parasites [J].
Bougdour, Alexandre ;
Maubon, Daniele ;
Baldacci, Patricia ;
Ortet, Philippe ;
Bastien, Olivier ;
Bouillon, Anthony ;
Barale, Jean-Christophe ;
Pelloux, Herve ;
Menard, Robert ;
Hakimi, Mohamed-Ali .
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 [J].
Buggy, JJ ;
Sideris, ML ;
Mak, P ;
Lorimer, DD ;
McIntosh, B ;
Clark, JM .
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 [J].
Chen, Chi-qi ;
Yu, Kang ;
Yan, Qing-xian ;
Xing, Chong-yun ;
YiChen ;
Yan, Zhuang ;
Shi, Yi-fen ;
Zhao, Ke-Wen ;
Gao, Shen-meng .
CARCINOGENESIS, 2013, 34 (07) :1442-1449
[10]   Lysine Acetylation Targets Protein Complexes and Co-Regulates Major Cellular Functions [J].
Choudhary, Chunaram ;
Kumar, Chanchal ;
Gnad, Florian ;
Nielsen, Michael L. ;
Rehman, Michael ;
Walther, Tobias C. ;
Olsen, Jesper V. ;
Mann, Matthias .
SCIENCE, 2009, 325 (5942) :834-840