Place your BETs: the therapeutic potential of bromodomains

被引:174
作者
Prinjha, R. K. [1 ]
Witherington, J. [1 ]
Lee, K. [1 ]
机构
[1] GlaxoSmithKline PLC, Med Res Ctr, Immunoinflammat Ctr Excellence Drug Discovery, Epinova DPU, Stevenage SG1 2NY, Herts, England
关键词
CHROMATIN-REMODELING COMPLEX; BIPOLAR AFFECTIVE-DISORDER; PAPILLOMAVIRUS E2 PROTEIN; HOST MITOTIC CHROMOSOMES; NUCLEAR-BODY; BAF COMPLEX; HISTONE MODIFICATIONS; SUSCEPTIBILITY LOCI; STRUCTURAL BASIS; GENE-EXPRESSION;
D O I
10.1016/j.tips.2011.12.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Therapeutic targeting of the processes that regulate histone modification is a growing area of scientific exploration. Although most interest has concentrated on the various families of enzymes that contribute to these processes, this review focuses on emerging data demonstrating the chemical tractability and therapeutic potential of a hitherto underexplored family of proteins, namely the bromodomain (BRD) family of reader proteins. These proteins perform a crucial role in translating histone modifications with powerful transcriptional consequences. We review current knowledge of the biology of this emergent target class and highlight recent breakthroughs that now make the BRD family of reader proteins attractive for drug discovery.
引用
收藏
页码:146 / 153
页数:8
相关论文
共 82 条
  • [1] Adachi Kea, 2006, Thienotriazolodiazepine compound and a medicinal use thereof, Patent No. [PCT/JP2006/310709, 2006310709]
  • [2] Deletion of the Proline-Rich Region of the Murine Metastasis Susceptibility Gene Brd4 Promotes Epithelial-to-Mesenchymal Transition- and Stem Cell-Like Conversion
    Alsarraj, Jude
    Walker, Renard C.
    Webster, Joshua D.
    Geiger, Thomas R.
    Crawford, Nigel P. S.
    Simpson, R. Mark
    Ozato, Keiko
    Hunter, Kent W.
    [J]. CANCER RESEARCH, 2011, 71 (08) : 3121 - 3131
  • [3] Histone methylation: Dynamic or static?
    Bannister, AJ
    Schneider, R
    Kouzarides, T
    [J]. CELL, 2002, 109 (07) : 801 - 806
  • [4] Regulation of chromatin by histone modifications
    Bannister, Andrew J.
    Kouzarides, Tony
    [J]. CELL RESEARCH, 2011, 21 (03) : 381 - 395
  • [5] DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS
    Bartsch, O
    Schmidt, S
    Richter, M
    Morlot, S
    Seemanová, E
    Wiebe, G
    Rasi, S
    [J]. HUMAN GENETICS, 2005, 117 (05) : 485 - 493
  • [6] Obesity genes and insulin resistance
    Belkina, Anna C.
    Denis, Gerald V.
    [J]. CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2010, 17 (05) : 472 - 477
  • [7] Perceptions of epigenetics
    Bird, Adrian
    [J]. NATURE, 2007, 447 (7143) : 396 - 398
  • [8] Conserved P-TEFb-interacting domain of BRD4 inhibits HIV transcription
    Bisgrovet, Dwayne A.
    Mahmoudi, Tokameh
    Henklein, Peter
    Verdin, Eric
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (34) : 13690 - 13695
  • [9] Identification and characterization of a leukocyte-specific component of the nuclear body
    Bloch, DB
    delaMonte, SM
    Guigaouri, P
    Filippov, A
    Bloch, KD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (46) : 29198 - 29204
  • [10] A Small Molecule Binding to the Coactivator CREB-Binding Protein Blocks Apoptosis in Cardiomyocytes
    Borah, Jagat C.
    Mujtaba, Shiraz
    Karakikes, Ioannis
    Zeng, Lei
    Muller, Michaela
    Patel, Jigneshkumar
    Moshkina, Natasha
    Morohashi, Keita
    Zhang, Weijia
    Gerona-Navarro, Guillermo
    Hajjar, Roger J.
    Zhou, Ming-Ming
    [J]. CHEMISTRY & BIOLOGY, 2011, 18 (04): : 531 - 541