Doxorubicin, DNA torsion, and chromatin dynamics

被引:638
作者
Yang, Fan [1 ]
Teves, Sheila S. [1 ]
Kemp, Christopher J. [2 ]
Henikoff, Steven [1 ,3 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Human Biol Div, Seattle, WA 98109 USA
[3] Howard Hughes Med Inst, Seattle, WA 98109 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2014年 / 1845卷 / 01期
关键词
Doxorubicin; Anthracycline; Cancer; DNA torsion; Chromatin dynamics; Chemotherapy; ANTITUMOR DRUGS ADRIAMYCIN; TOPOISOMERASE-II; CANCER-CELLS; NUCLEOSOME TURNOVER; IN-VIVO; INDUCED CARDIOTOXICITY; MULTIDRUG-RESISTANCE; MAGNETIC TWEEZERS; MOLECULAR-BASIS; BREAST-CANCER;
D O I
10.1016/j.bbcan.2013.12.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Doxorubicin is one of the most important anti-cancer chemotherapeutic drugs, being widely used for the treatment of solid tumors and acute leukemias. The action of doxorubicin and other anthracydine drugs has been intensively investigated during the last several decades, but the mechanisms that have been proposed for cell killing remain disparate and controversial. In this review, we examine the proposed models for doxorubicin action from the perspective of the chromatin landscape, which is altered in many types of cancer due to recurrent mutations in chromatin modifiers. We highlight recent evidence for effects of anthracyclines on DNA torsion and chromatin dynamics that may underlie basic mechanisms of doxorubicin-mediated cell death and suggest new therapeutic strategies for cancer treatment. (c) 2013 The Authors. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 89
页数:6
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