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
  • [1] Dissecting Histone Deacetylase 3 in Multiple Disease Conditions: Selective Inhibition as a Promising Therapeutic Strategy
    Adhikari, Nilanjan
    Jha, Tarun
    Ghosh, Balaram
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2021, 64 (13) : 8827 - 8869
  • [2] Selective and nonselective HDAC8 inhibitors: a therapeutic patent review
    Adhikari, Nilanjan
    Amin, Sk Abdul
    Jha, Tarun
    [J]. PHARMACEUTICAL PATENT ANALYST, 2018, 7 (06) : 259 - 276
  • [3] Structure-activity relationships of hydroxamate-based histone deacetylase-8 inhibitors: reality behind anticancer drug discovery
    Amin, S. K. Abdul
    Adhikari, Nilanjan
    Jha, Tarun
    [J]. FUTURE MEDICINAL CHEMISTRY, 2017, 9 (18) : 2211 - 2237
  • [4] Structure-activity relationships of HDAC8 inhibitors: Non-hydroxamates as anticancer agents
    Amin, Sk. Abdul
    Adhikari, Nilanjan
    Jha, Tarun
    [J]. PHARMACOLOGICAL RESEARCH, 2018, 131 : 128 - 142
  • [5] HDAC8 promotes the dissemination of breast cancer cells via AKT/GSK-3β/Snail signals
    An, Panpan
    Chen, Feng
    Li, Zihan
    Ling, Yuyi
    Peng, Yanxi
    Zhang, Haisheng
    Li, Jiexin
    Chen, Zhuojia
    Wang, Hongsheng
    [J]. ONCOGENE, 2020, 39 (26) : 4956 - 4969
  • [6] Histone deacetylase 8 triggers the migration of triple negative breast cancer cells via regulation of YAP signals
    An, Panpan
    Li, Jiexin
    Lu, Linlin
    Wu, Yingmin
    Ling, Yuyi
    Du, Jun
    Chen, Zhuojia
    Wang, Hongsheng
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2019, 845 : 16 - 23
  • [7] HDAC8-inhibitor PCI-34051-induced exosomes inhibit human bronchial smooth muscle cell proliferation via miR-381-3p mediated TGFB3
    Bai, Shi-Yao
    Li, Meng-Lu
    Ren, Yuan
    Su, Xin-Ming
    [J]. PULMONARY PHARMACOLOGY & THERAPEUTICS, 2021, 71
  • [8] 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
  • [9] Balasubramanian S., 2008, BLOOD, V112, P2581, DOI DOI 10.1182/blood.V112.11.3366.3366
  • [10] Isoform-specific histone deacetylase inhibitors: The next step?
    Balasubramanian, Sriram
    Verner, Erik
    Buggy, Joseph J.
    [J]. CANCER LETTERS, 2009, 280 (02) : 211 - 221