HDAC8 as an emerging target in drug discovery with special emphasis on medicinal chemistry

被引:6
作者
Rajaraman, Srinidhi [1 ]
Balakrishnan, Ranjani [1 ]
Deshmukh, Dhruv [1 ]
Ganorkar, Abhiram [1 ]
Biswas, Swati [1 ]
Pulya, Sravani [1 ]
Ghosh, Balaram [1 ]
机构
[1] Birla Inst Technol & Sci Pilani, Dept Pharm, Epigenet Res Lab, Hyderabad Campus, Hyderabad 500078, India
关键词
cancer; epigenetic modulator; HDAC8 selective inhibitor; histone deacetylase 8; structure-activity relationship; HISTONE DEACETYLASE 8; ZINC-BINDING GROUPS; BIOLOGICAL EVALUATION; BENZAMIDE CLASS; INHIBITORS; DESIGN; ACETYLATION; CANCER; CLONING; CELLS;
D O I
10.4155/fmc-2023-0054
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
HDAC8 catalyzes the deacetylation of both histones and nonhistone proteins. The abnormal expression of HDAC8 is associated with various pathological conditions causing cancer and other diseases like myopathies, Cornelia de Lange syndrome, renal fibrosis, and viral and parasitic infections. The substrates of HDAC8 are involved in diverse molecular mechanisms of cancer such as cell proliferation, invasion, metastasis and drug resistance. Based on the crystal structures and the key residues at the active site, HDAC8 inhibitors have been designed along the canonical pharmacophore. This article details the importance, recent advancements, and the structural and functional aspects of HDAC8 with special emphasis on the medicinal chemistry aspect of HDAC8 inhibitors that will help in developing novel epigenetic therapeutics.
引用
收藏
页码:885 / 908
页数:24
相关论文
共 133 条
  • [11] Histone deacetylase 8 (HDAC8) and its inhibitors with selectivity to other isoforms: An overview
    Banerjee, Suvankar
    Adhikari, Nilanjan
    Amin, Sk Abdul
    Jha, Tarun
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2019, 164 : 214 - 240
  • [12] PROTAC targeted protein degraders: the past is prologue
    Bekes, Miklos
    Langley, David R.
    Crews, Craig M.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2022, 21 (03) : 181 - 200
  • [13] Epigenetics - An epicenter of gene regulation: Histones and histone-modifying enzymes
    Biel, M
    Wascholowski, V
    Giannis, A
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (21) : 3186 - 3216
  • [14] Perceptions of epigenetics
    Bird, Adrian
    [J]. NATURE, 2007, 447 (7143) : 396 - 398
  • [15] 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
  • [16] Histone deacetylase inhibitors prevent exocytosis of interleukin-1β-containing secretory lysosomes:: role of microtubules
    Carta, Sonia
    Tassi, Sara
    Semino, Claudia
    Fossati, Gianluca
    Mascagni, Paolo
    Dinarello, Charles A.
    Rubartelli, Anna
    [J]. BLOOD, 2006, 108 (05) : 1618 - 1626
  • [17] Targeting histone deacetylase 8 as a therapeutic approach to cancer and neurodegenerative diseases
    Chakrabarti, Alokta
    Melesina, Jelena
    Kolbinger, Fiona R.
    Oehme, Ina
    Senger, Johanna
    Witt, Olaf
    Sippl, Wolfgang
    Jung, Manfred
    [J]. FUTURE MEDICINAL CHEMISTRY, 2016, 8 (13) : 1609 - 1634
  • [18] HDAC8: a multifaceted target for therapeutic interventions
    Chakrabarti, Alokta
    Oehme, Ina
    Witt, Olaf
    Oliveira, Guilherme
    Sippl, Wolfgang
    Romier, Christophe
    Pierce, Raymond J.
    Jung, Manfred
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2015, 36 (07) : 481 - 492
  • [19] Inhibition and Mechanism of HDAC8 Revisited
    Chen, Kai
    Zhang, Xiaoxiao
    Wu, Yun-Dong
    Wiest, Olaf
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (33) : 11636 - 11643
  • [20] Protein degraders enter the clinic - a new approach to cancer therapy
    Chirnomas, Deborah
    Hornberger, Keith R.
    Crews, Craig M.
    [J]. NATURE REVIEWS CLINICAL ONCOLOGY, 2023, 20 (04) : 265 - 278