Epigenetic strategies in cancer therapy

被引:0
作者
Hessmann, E. [1 ]
Johnsen, S. A. [2 ]
Ellenrieder, V. [1 ]
机构
[1] Univ Med Gottingen, Klin Gastroenterol & Gastrointestinale Onkol, Robert Koch Str 40, D-37075 Gottingen, Germany
[2] Univ Med Gottingen, Klin Allgemein Viszeral & Kinderchirurg, D-37075 Gottingen, Germany
来源
ONKOLOGE | 2016年 / 22卷 / 01期
关键词
Epigenetics; Epigenetic cancer therapy; Personalized medicine; DNA methylation; Histone modification; MULTIPLE-MYELOMA; INHIBITION; METHYLTRANSFERASE; PANOBINOSTAT; BORTEZOMIB; TARGETS; DOT1L;
D O I
10.1007/s00761-015-2998-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Experimental insights into epigenetic regulatory mechanisms have dramatically altered our understanding of malignant diseases and demonstrated that, in addition to genetic alterations, epigenetic changes significantly contribute to cancer development and progression. Consequently, epigenetic mechanisms are considered to be core components of prospective cancer therapies. The first epigenetic cancer drugs have been developed and are already being used in cancer treatment. Predominantly, these epigenetic treatments inhibit enzymes, such as DNA methyltransferase inhibitors and inhibitors of histone deacetylases, which add or remove epigenetic modifications. Some substances have already been approved for the treatment of selected malignancies or are currently undergoing testing in clinical trials. The rationale behind the application of epigenetic inhibitors is to modulate undesired epigenetic DNA and histone modifications in order to restore the normal expression of tumor suppressor genes or restrict the transcriptional activity of oncogenes. Conclusion. Novel epigenetic approaches, such as inhibition of histone methyltransferases and oncogenic chromatin complexes have not yet achieved clinical approval but are being intensively studied in preclinical and clinical trials and represent promising candidates for cancer therapy.
引用
收藏
页码:19 / +
页数:8
相关论文
共 31 条
[1]   The diverse functions of Dot1 and H3K79 methylation [J].
Anh Tram Nguyen ;
Zhang, Yi .
GENES & DEVELOPMENT, 2011, 25 (13) :1345-1358
[2]   First-in-human, Pharmacokinetic and Pharmacodynamic Phase I Study of Resminostat, an Oral Histone Deacetylase Inhibitor, in Patients with Advanced Solid Tumors [J].
Brunetto, Andre T. ;
Ang, Joo Ern ;
Lal, Rohit ;
Olmos, David ;
Molife, L. Rhoda ;
Kristeleit, Rebecca ;
Parker, Ann ;
Casamayor, Isabel ;
Olaleye, Muyibat ;
Mais, Anna ;
Hauns, Bernhard ;
Strobel, Vera ;
Hentsch, Bernd ;
de Bono, Johann S. .
CLINICAL CANCER RESEARCH, 2013, 19 (19) :5494-5504
[3]   Dual kinase-bromodomain inhibitors for rationally designed polypharmacology [J].
Ciceri, Pietro ;
Mueller, Susanne ;
O'Mahony, Alison ;
Fedorov, Oleg ;
Filippakopoulos, Panagis ;
Hunt, Jeremy P. ;
Lasater, Elisabeth A. ;
Pallares, Gabriel ;
Picaud, Sarah ;
Wells, Christopher ;
Martin, Sarah ;
Wodicka, Lisa M. ;
Shah, Neil P. ;
Treiber, Daniel K. ;
Knapp, Stefan .
NATURE CHEMICAL BIOLOGY, 2014, 10 (04) :305-+
[4]   Potent inhibition of DOT1L as treatment of MLL-fusion leukemia [J].
Daigle, Scott R. ;
Olhava, Edward J. ;
Therkelsen, Carly A. ;
Basavapathruni, Aravind ;
Jin, Lei ;
Boriack-Sjodin, P. Ann ;
Allain, Christina J. ;
Klaus, Christine R. ;
Raimondi, Alejandra ;
Scott, Margaret Porter ;
Waters, Nigel J. ;
Chesworth, Richard ;
Moyer, Mikel P. ;
Copeland, Robert A. ;
Richon, Victoria M. ;
Pollock, Roy M. .
BLOOD, 2013, 122 (06) :1017-1025
[5]   Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia [J].
Dawson, Mark A. ;
Prinjha, Rab K. ;
Dittmann, Antje ;
Giotopoulos, George ;
Bantscheff, Marcus ;
Chan, Wai-In ;
Robson, Samuel C. ;
Chung, Chun-wa ;
Hopf, Carsten ;
Savitski, Mikhail M. ;
Huthmacher, Carola ;
Gudgin, Emma ;
Lugo, Dave ;
Beinke, Soren ;
Chapman, Trevor D. ;
Roberts, Emma J. ;
Soden, Peter E. ;
Auger, Kurt R. ;
Mirguet, Olivier ;
Doehner, Konstanze ;
Delwel, Ruud ;
Burnett, Alan K. ;
Jeffrey, Phillip ;
Drewes, Gerard ;
Lee, Kevin ;
Huntly, Brian J. P. ;
Kouzarides, Tony .
NATURE, 2011, 478 (7370) :529-533
[6]   BET Bromodomain Inhibition as a Therapeutic Strategy to Target c-Myc [J].
Delmore, Jake E. ;
Issa, Ghayas C. ;
Lemieux, Madeleine E. ;
Rahl, Peter B. ;
Shi, Junwei ;
Jacobs, Hannah M. ;
Kastritis, Efstathios ;
Gilpatrick, Timothy ;
Paranal, Ronald M. ;
Qi, Jun ;
Chesi, Marta ;
Schinzel, Anna C. ;
McKeown, Michael R. ;
Heffernan, Timothy P. ;
Vakoc, Christopher R. ;
Bergsagel, P. Leif ;
Ghobrial, Irene M. ;
Richardson, Paul G. ;
Young, Richard A. ;
Hahn, William C. ;
Anderson, Kenneth C. ;
Kung, Andrew L. ;
Bradner, James E. ;
Mitsiades, Constantine S. .
CELL, 2011, 146 (06) :903-916
[7]   Concise Drug Review: Azacitidine and Decitabine [J].
Derissen, Ellen J. B. ;
Beijnen, Jos H. ;
Schellens, Jan H. M. .
ONCOLOGIST, 2013, 18 (05) :619-624
[8]   Development and classes of epigenetic drugs for cancer [J].
Dhanak, Dashyant ;
Jackson, Paul .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 455 (1-2) :58-69
[9]   Selective inhibition of BET bromodomains [J].
Filippakopoulos, Panagis ;
Qi, Jun ;
Picaud, Sarah ;
Shen, Yao ;
Smith, William B. ;
Fedorov, Oleg ;
Morse, Elizabeth M. ;
Keates, Tracey ;
Hickman, Tyler T. ;
Felletar, Ildiko ;
Philpott, Martin ;
Munro, Shonagh ;
McKeown, Michael R. ;
Wang, Yuchuan ;
Christie, Amanda L. ;
West, Nathan ;
Cameron, Michael J. ;
Schwartz, Brian ;
Heightman, Tom D. ;
La Thangue, Nicholas ;
French, Christopher A. ;
Wiest, Olaf ;
Kung, Andrew L. ;
Knapp, Stefan ;
Bradner, James E. .
NATURE, 2010, 468 (7327) :1067-1073
[10]   Identification of EZH2 and EZH1 Small Molecule Inhibitors with Selective Impact on Diffuse Large B Cell Lymphoma Cell Growth [J].
Garapaty-Rao, Shivani ;
Nasveschuk, Christopher ;
Gagnon, Alexandre ;
Chan, Eric Y. ;
Sandy, Peter ;
Busby, Jennifer ;
Balasubramanian, Srividya ;
Campbell, Robert ;
Zhao, Feng ;
Bergeron, Louise ;
Audia, James E. ;
Albrecht, Brian K. ;
Harmange, Jean-Christophe ;
Cummings, Richard ;
Trojer, Patrick .
CHEMISTRY & BIOLOGY, 2013, 20 (11) :1329-1339