New anti-cancer strategies: Epigenetic therapies and biomarkers

被引:47
作者
Balch, C
Montgomery, JS
Paik, HI
Kim, S
Huang, THM
Nephew, KP
机构
[1] Indiana Univ, Med Sci Program, Bloomington, IN 47405 USA
[2] Indiana Univ, Sch Informat, Bloomington, IN 47408 USA
[3] Indiana Univ, Ctr Genom & Bioinformat, Bloomington, IN 47405 USA
[4] Ohio State Univ, Ctr Comprehens Canc, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[5] Indiana Univ, Ctr Canc, Indianapolis, IN 46202 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2005年 / 10卷
关键词
biomarkers; bioinformatics; cancer; chemotherapy; chemosensitization; DNA methylation; drug resistance; epigenetics; epigenetic biomarkers; epigenetic therapies; HDAC; HDAC inhibitor; histone deacetylase; methylation; methylation biomarkers; methyltransferase; review;
D O I
10.2741/1668
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Epigenetics is the study of chromatin modifications that affect gene expression without altering DNA nucleotide sequences. This review highlights a prominent role for epigenetic therapies, particularly those that reverse aberrant DNA methylation and histone acetylation, in the potential treatment of cancer. Administration of such therapies to reverse epigenetic "silencing" of tumor suppressors, including genes involved in chemotherapy responses, could prove useful in the management of cancer patients. In this review, we summarize recent advances in the use of methyltransferase and histone deacetylase inhibitors and possible synergistic combinations of these to achieve maximal tumor suppressor gene re-expression. Moreover, when used in combination with conventional chemotherapeutic agents, epigenetic-based therapies may provide a means to resensitize drug-resistant tumors to established treatments. As specific, aberrant epigenetic modifications are frequently associated with distinct cancer types, and likely occur early in tumorigenesis, these have potential utility as biomarkers. Finally, future directions are addressed, including alternative epigenetic targets, gene-specific modifications, and the use of bioinformatics.
引用
收藏
页码:1897 / 1931
页数:35
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