Epigenetic Targeting Therapies to Overcome Chemotherapy Resistance

被引:20
|
作者
Balch, Curt [1 ,2 ]
Nephew, Kenneth P. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Indiana Univ Sch Med, Bloomington, IN 47405 USA
[2] Indiana Univ, Melvin & Bren Simon Canc Ctr, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Dept Cellular & Integrat Physiol, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Dept Med, Dept Obstet & Gynecol, Indianapolis, IN 46202 USA
[5] Indiana Univ Sch Med, Dept Cellular & Integrat Physiol, Med Sci Program, Bloomington, IN 47405 USA
来源
基金
美国国家卫生研究院;
关键词
HISTONE DEACETYLASE INHIBITOR; TUMOR-SUPPRESSOR GENES; SUBEROYLANILIDE HYDROXAMIC ACID; LOW-DOSE 5-AZA-2'-DEOXYCYTIDINE; BREAST-CANCER CELLS; DNA-HYPOMETHYLATING AGENT; ACUTE MYELOID-LEUKEMIA; PHASE-II TRIAL; EPITHELIAL OVARIAN-CANCER; CISPLATIN PLUS DECITABINE;
D O I
10.1007/978-1-4419-9967-2_14
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is now well established that epigenetic aberrations occur early in malignant transformation, raising the possibility of identifying chemopreventive compounds or reliable diagnostic screening using epigenetic biomarkers. Combinatorial therapies effective for the reexpression of tumor suppressors, facilitating resensitization to conventional chemotherapies, hold great promise for the future therapy of cancer. This approach may also perturb cancer stem cells and thus represent an effective means for managing a number of solid tumors. We believe that in the near future, anticancer drug regimens will routinely include epigenetic therapies, possibly in conjunction with inhibitors of "stemness" signal pathways, to effectively reduce the devastating occurrence of cancer chemotherapy resistance.
引用
收藏
页码:285 / 311
页数:27
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