Epigenetic Therapy: Histone Acetylation, DNA Methylation and Anti-Cancer Drug Discovery

被引:78
作者
Ganesan, A. [2 ]
Nolan, L. [1 ]
Crabb, S. J. [1 ]
Packham, G. [1 ]
机构
[1] Univ Southampton, Southampton Gen Hosp, Canc Res UK Ctr, Canc Sci Div,Sch Med, Southampton SO16 6YD, Hants, England
[2] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
关键词
Epigenetic; chromatin; histone; DNA methylation; acetylation; histone deacetylase; inhibitor; BREAST-CANCER CELLS; SUBEROYLANILIDE HYDROXAMIC ACID; MESSENGER-RNA EXPRESSION; TRANS-RETINOIC ACID; PHASE-I TRIAL; DEACETYLASE INHIBITOR BELINOSTAT; CISPLATIN PLUS DECITABINE; SMALL-MOLECULE INHIBITOR; ADVANCED SOLID TUMORS; LOW-DOSE DECITABINE;
D O I
10.2174/156800909790192428
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Histone proteins are subject to a diverse range of post-translational modifications which, along with DNA methylation, play a major role in controlling gene expression, cell division, survival and differentiation. Alterations in these chromatin modifications are thought to contribute to important human diseases including cancer. Inhibition of the enzymes that introduce and remove these chromatin modifications is proving an effective approach to cancer therapy and inhibitors of histone deacetylases and DNA methyltransferases have been approved for use in haematological malignancies. Here we provide a background to the biology of chromatin modifications and review some of the evidence validating histone deacetylases and DNA methyltransferases as targets for anti-cancer drug discovery. We then focus on two of the key issues in this field; the identification of novel inhibitors to overcome shortcomings of first generation agents and the potential role of histone deacetylase and DNA methyltransferase inhibitors in combination therapies for oncology. Finally, we highlight some of the challenges that will need to addressed to further progress the development of epigenetic-based therapies for cancer.
引用
收藏
页码:963 / 981
页数:19
相关论文
共 223 条
[1]
ARTS J, 2008, Patent No. 2008031817
[2]
Valproic acid (VPA) in patients with refractory advanced cancer:: a dose escalating phase I clinical trial [J].
Atmaca, A. ;
Al-Batran, S-E ;
Maurer, A. ;
Neumann, A. ;
Heinzel, T. ;
Hentsch, B. ;
Schwarz, S. E. ;
Hovelmann, S. ;
Goettlicher, M. ;
Knuth, A. ;
Jaeger, E. .
BRITISH JOURNAL OF CANCER, 2007, 97 (02) :177-182
[3]
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
[4]
Isoform-specific histone deacetylase inhibitors: The next step? [J].
Balasubramanian, Sriram ;
Verner, Erik ;
Buggy, Joseph J. .
CANCER LETTERS, 2009, 280 (02) :211-221
[5]
Activity of suberoylanilide hydroxamic acid against human breast cancer cells with amplification of Her-2 [J].
Bali, P ;
Pranpat, M ;
Swaby, R ;
Fiskus, W ;
Yamaguchi, H ;
Balasis, M ;
Rocha, K ;
Wang, HG ;
Richon, V ;
Bhalla, K .
CLINICAL CANCER RESEARCH, 2005, 11 (17) :6382-6389
[6]
Histone deacetylase inhibitors in combinations: Will the preclinical promises be kept? [J].
Bates, Susan E. ;
Piekarz, Richard L. .
CANCER JOURNAL, 2007, 13 (02) :80-83
[7]
Distinct pharmacological properties of second generation HDAC inhibitors with the benzamide or hydroxamate head group [J].
Beckers, Thomas ;
Burkhardt, Carmen ;
Wieland, Heike ;
Gimmnich, Petra ;
Ciossek, Thomas ;
Maier, Thomas ;
Sanders, Karl .
INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (05) :1138-1148
[8]
Covalent modifications of histones during development and disease pathogenesis [J].
Bhaumik, Sukesh R. ;
Smith, Edwin ;
Shilatifard, Ali .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2007, 14 (11) :1008-1016
[9]
Anticancer activities of histone deacetylase inhibitors [J].
Bolden, Jessica E. ;
Peart, Melissa J. ;
Johnstone, Ricky W. .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (09) :769-784
[10]
Evaluation of the pharmacodynamic effects of MGCD0103 from preclinical models to human using a novel HDAC enzyme assay [J].
Bonfils, Claire ;
Kalita, Ann ;
Dubay, Marja ;
Siu, Lillian L. ;
Carducci, Michael A. ;
Reid, Gregory ;
Martell, Robert E. ;
Besterman, Jeffrey M. ;
Li, Zuomei .
CLINICAL CANCER RESEARCH, 2008, 14 (11) :3441-3449