Altering DNA Repair to Improve Radiation Therapy: Specific and Multiple Pathway Targeting

被引:99
作者
Biau, Julian [1 ,2 ,3 ,4 ,5 ,6 ]
Chautard, Emmanuel [5 ,7 ]
Verrelle, Pierre [1 ,6 ,8 ,9 ]
Dutreix, Marie [1 ,2 ,3 ,4 ]
机构
[1] PSL Res Univ, Ctr Rech, Inst Curie, Paris, France
[2] CNRS, UMR3347, Orsay, France
[3] INSERM, U1021, Orsay, France
[4] Univ Paris Sud, Orsay, France
[5] Univ Clermont Auvergne, IMoST U1240, INSERM, Clermont Ferrand, France
[6] Univ Clermont Auvergne, Ctr Jean Perrin, Radiotherapy Dept, Clermont Ferrand, France
[7] Univ Clermont Auvergne, Ctr Jean Perrin, Pathol Dept, Clermont Ferrand, France
[8] CNRS, UMR9187, INSERM, U1196, Orsay, France
[9] Inst Curie Hosp, Radiotherapy Dept, Paris, France
关键词
DNA damage; repair systems; radiotherapy; radioresistance; inhibition; BASE EXCISION-REPAIR; STRAND BREAK REPAIR; DEPENDENT PROTEIN-KINASE; HISTONE DEACETYLASE INHIBITOR; SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR RECEPTOR; HUMAN TUMOR-CELLS; IONIZING-RADIATION; IN-VITRO; PHASE-I;
D O I
10.3389/fonc.2019.01009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Radiation therapy (RT) is widely used in cancer care strategies. Its effectiveness relies mainly on its ability to cause lethal damage to the DNA of cancer cells. However, some cancers have shown to be particularly radioresistant partly because of efficient and redundant DNA repair capacities. Therefore, RT efficacy might be enhanced by using drugs that can disrupt cancer cells' DNA repair machinery. Here we review the recent advances in the development of novel inhibitors of DNA repair pathways in combination with RT. A large number of these compounds are the subject of preclinical/clinical studies and target key enzymes involved in one or more DNA repair pathways. A totally different strategy consists of mimicking DNA double-strand breaks via small interfering DNA (siDNA) to bait the whole DNA repair machinery, leading to its global inhibition.
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页数:10
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