DNA damage and metabolic mechanisms of cancer drug resistance

被引:18
|
作者
Tiek, Deanna [1 ,2 ]
Cheng, Shi-Yuan [1 ,2 ]
机构
[1] Northwestern Univ, Ken & Ruth Davee Dept Neurol, Lou & Jean Malnati Brain Tumor Inst Northwestern, Robert H Lurie Comprehens Canc Ctr,Feinberg Sch M, 303 E Super St, Chicago, IL 60611 USA
[2] Northwestern Univ, Simpson Querry Inst Epigenet, Feinberg Sch Med, 303 E Super St, Chicago, IL 60611 USA
关键词
Cancer drug resistance; drug resistance; metabolism; DNA damage; DNA repair; hypoxia; synthetic lethality; overcoming resistance; PHASE-II TRIAL; HYDROGEN-PEROXIDE; CELLS; INHIBITOR; INACTIVATION; FERROPTOSIS; HYPOXIA; GENE; PH; TEMOZOLOMIDE;
D O I
10.20517/cdr.2021.148
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer drug resistance is one of the main barriers to overcome to ensure durable treatment responses. While many pivotal advances have been made in first combination therapies, then targeted therapies, and now broadening out to immunomodulatory drugs or metabolic targeting compounds, drug resistance is still ultimately universally fatal. In this brief review, we will discuss different strategies that have been used to fight drug resistance from synthetic lethality to tumor microenvironment modulation, focusing on the DNA damage response and tumor metabolism both within tumor cells and their surrounding microenvironment. In this way, with a better understanding of both targetable mutations in combination with the metabolism, smarter drugs may be designed to combat cancer drug resistance.
引用
收藏
页码:368 / 379
页数:12
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