Emerging Epigenetic Targets and Therapies in Cancer Medicine

被引:91
作者
Popovic, Relja [1 ]
Licht, Jonathan D. [1 ]
机构
[1] Northwestern Univ, Div Hematol Oncol, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Chicago, IL 60611 USA
关键词
ACUTE MYELOID-LEUKEMIA; GLOBAL HISTONE METHYLATION; CELL-CYCLE PROGRESSION; CENTER B-CELLS; GENE-EXPRESSION; TRANSCRIPTION ELONGATION; SOMATIC MUTATIONS; H3K79; METHYLATION; BET BROMODOMAINS; IDH2; MUTATIONS;
D O I
10.1158/2159-8290.CD-12-0076
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Abnormalities in the epigenetic regulation of chromatin structure and function can lead to aberrant gene expression and cancer development. Consequently, epigenetic therapies aim to restore normal chromatin modification patterns through the inhibition of various components of the epigenetic machinery. Histone deacetylase and DNA methyltransferase inhibitors represent the first putative epigenetic therapies; however, these agents have pleiotropic effects and it remains unclear how they lead to therapeutic responses. More recently, drugs that inhibit histone methyltransferases were developed, perhaps representing more specific agents. We review emerging epigenetic targets in cancer and present recent models of promising epigenetic therapies. Significance: The use of DNA methyltransferase and histone deacetylase inhibitors in patients has validated the use of drugs targeted to epigenetic enzymes and strengthened the need for development of additional therapies. In this review, we summarize recently discovered epigenetic abnormalities, their implications for cancer, and the approaches taken for discovering small-molecule inhibitors-targeting various properties of the epigenetic machinery. Cancer Discov; 2(5);405-13. (c) 2012 AACR.
引用
收藏
页码:405 / 413
页数:9
相关论文
共 78 条
[1]   UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development [J].
Agger, Karl ;
Cloos, Paul A. C. ;
Christensen, Jesper ;
Pasini, Diego ;
Rose, Simon ;
Rappsilber, Juri ;
Issaeva, Irina ;
Canaani, Eli ;
Salcini, Anna Elisabetta ;
Helin, Kristian .
NATURE, 2007, 449 (7163) :731-U10
[2]   Histone methyltransferases in cancer [J].
Albert, Mareike ;
Helin, Kristian .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2010, 21 (02) :209-220
[3]   IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours [J].
Amary, M. Fernanda ;
Bacsi, Krisztian ;
Maggiani, Francesca ;
Damato, Stephen ;
Halai, Dina ;
Berisha, Fitim ;
Pollock, Robin ;
O'Donnell, Paul ;
Grigoriadis, Anita ;
Diss, Tim ;
Eskandarpour, Malihe ;
Presneau, Nadege ;
Hogendoorn, Pancras C. W. ;
Futreal, Andrew ;
Tirabosco, Roberto ;
Flanagan, Adrienne M. .
JOURNAL OF PATHOLOGY, 2011, 224 (03) :334-343
[4]   NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines [J].
Angrand, PO ;
Apiou, F ;
Stewart, AF ;
Dutrillaux, B ;
Losson, R ;
Chambon, P .
GENOMICS, 2001, 74 (01) :79-88
[5]  
[Anonymous], 2012, CAT SOM MUT CANC
[6]   ES Cell Cycle Progression and Differentiation Require the Action of the Histone Methyltransferase Dot1L [J].
Barry, Evan R. ;
Krueger, Winfried ;
Jakuba, Caroline M. ;
Veilleux, Eric ;
Ambrosi, Dominic J. ;
Nelson, Craig E. ;
Rasmussen, Theodore P. .
STEM CELLS, 2009, 27 (07) :1538-1547
[7]   High-resolution profiling of histone methylations in the human genome [J].
Barski, Artern ;
Cuddapah, Suresh ;
Cui, Kairong ;
Roh, Tae-Young ;
Schones, Dustin E. ;
Wang, Zhibin ;
Wei, Gang ;
Chepelev, Iouri ;
Zhao, Keji .
CELL, 2007, 129 (04) :823-837
[8]   The etiology of Wolf-Hirschhorn syndrome [J].
Bergemann, AD ;
Cole, F ;
Hirschhorn, K .
TRENDS IN GENETICS, 2005, 21 (03) :188-195
[9]   MLL-Rearranged Leukemia Is Dependent on Aberrant H3K79 Methylation by DOT1L [J].
Bernt, Kathrin M. ;
Zhu, Nan ;
Sinha, Amit U. ;
Vempati, Sridhar ;
Faber, Joerg ;
Krivtsov, Andrei V. ;
Feng, Zhaohui ;
Punt, Natalie ;
Daigle, Amanda ;
Bullinger, Lars ;
Pollock, Roy M. ;
Richon, Victoria M. ;
Kung, Andrew L. ;
Armstrong, Scott A. .
CANCER CELL, 2011, 20 (01) :66-78
[10]   The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling [J].
Bitoun, Emmanuelle ;
Oliver, Peter L. ;
Davies, Kay E. .
HUMAN MOLECULAR GENETICS, 2007, 16 (01) :92-106