The interplay between DNA topoisomerase 2α post-translational modifications and drug resistance

被引:16
作者
Lotz, Christophe [1 ]
Lamour, Valerie [1 ,2 ]
机构
[1] Univ Strasbourg, Integrat Struct Biol Dept, INSERM, IGBMC,U1258,CNRS,UMR 7104, F-67404 Illkirch Graffenstaden, France
[2] Hop Univ Strasbourg, F-67000 Strasbourg, France
关键词
DNA topoisomerase; drug resistance; post-translational modifications; etoposide;
D O I
10.20517/cdr.2019.114
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The type 2 DNA topoisomerases (Top2) are conserved enzymes and biomarkers for cell proliferation. The catalytic activities of the human isoform Top2 alpha are essential for the regulation of DNA topology during DNA replication, transcription, and chromosome segregation. Top2 alpha is a prominent target for anti-cancer drugs and is highly regulated by post-translational modifications (PTM). Despite an increasing number of proteomic studies, the extent of PTM in cancer cells and its importance in drug response remains largely uncharacterized. In this review, we highlight the different modifications affecting the human Top2 alpha in healthy and cancer cells, taking advantage of the structure-function information accumulated in the past decades. We also overview the regulation of Top2 alpha by PTM, the level of PTM in cancer cells, and the resistance to therapeutic compounds targeting the Top2 enzyme. Altogether, this review underlines the importance of future studies addressing more systematically the interplay between PTM and Top2 drug resistance.
引用
收藏
页码:149 / 160
页数:12
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