Epigenetic Pathways and Glioblastoma Treatment: Insights From Signaling Cascades

被引:23
作者
Allen, Bryce K. [1 ]
Stathias, Vasileios [1 ]
Maloof, Marie E. [1 ]
Vidovic, Dusica [2 ]
Winterbottom, Emily F. [3 ]
Capobianco, Anthony J. [3 ]
Clarke, Jennifer [4 ]
Schurer, Stephan [2 ]
Robbins, David J. [3 ]
Ayad, Nagi G. [1 ]
机构
[1] Univ Miami, Ctr Therapeut Innovat, Dept Psychiat & Behav Sci, Miami, FL 33136 USA
[2] Univ Miami, Ctr Computat Sci, Dept Mol & Cellular Pharmacol, Miami, FL 33136 USA
[3] Univ Miami, Dept Surg, Miami, FL 33136 USA
[4] Univ Nebraska, Dept Stat & Food Sci, Lincoln, NE 68506 USA
关键词
EPIGENETICS; GLIOBLASTOMA; SIGNALING PATHWAYS; HEDGEHOG; NOTCH; WINGLESS; HISTONE ACETYLTRANSFERASE PCAF; BASAL-CELL CARCINOMA; SONIC-HEDGEHOG; GLI PROTEINS; INHIBITION; ACTIVATION; SUPPRESSOR; FAMILY; MEDULLOBLASTOMA; ASSOCIATION;
D O I
10.1002/jcb.24990
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is an urgent need to identify novel therapies for glioblastoma (GBM) as most therapies are ineffective. A first step in this process is to identify and validate targets for therapeutic intervention. Epigenetic modulators have emerged as attractive drug targets in several cancers including GBM. These epigenetic regulators affect gene expression without changing the DNA sequence. Recent studies suggest that epigenetic regulators interact with drivers of GBM cell and stem-like cell proliferation. These drivers include components of the Notch, Hedgehog, and Wingless (WNT) pathways. We highlight recent studies connecting epigenetic and signaling pathways in GBM. We also review systems and big data approaches for identifying patient specific therapies in GBM. Collectively, these studies will identify drug combinations that may be effective in GBM and other cancers. (C) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:351 / 363
页数:13
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