Beyond DNA Repair: DNA-PK Function in Cancer

被引:198
作者
Goodwin, Jonathan F. [1 ]
Knudsen, Karen E. [1 ,2 ,3 ,4 ]
机构
[1] Thomas Jefferson Univ, Dept Canc Biol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Dept Urol, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Dept Radiat Oncol, Philadelphia, PA 19107 USA
[4] Thomas Jefferson Univ, Kimmel Canc Ctr, Philadelphia, PA 19107 USA
关键词
DEPENDENT-PROTEIN-KINASE; DOUBLE-STRAND BREAKS; RNA-POLYMERASE-II; ATAXIA-TELANGIECTASIA GENE; HUMAN GLIOBLASTOMA CELLS; ESTROGEN-RECEPTOR-ALPHA; HUMAN TUMOR-CELLS; CATALYTIC-SUBUNIT; HOMOLOGOUS RECOMBINATION; IONIZING-RADIATION;
D O I
10.1158/2159-8290.CD-14-0358
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The DNA-dependent protein kinase (DNA-PK) is a pivotal component of the DNA repair machinery that governs the response to DNA damage, serving to maintain genome integrity. However, the DNA-PK kinase component was initially isolated with transcriptional complexes, and recent findings have illuminated the impact of DNA-PK-mediated transcriptional regulation on tumor progression and therapeutic response. DNA-PK expression has also been correlated with poor outcome in selected tumor types, further underscoring the importance of understanding its role in disease. Herein, the molecular and cellular consequences of DNA-PK are considered, with an eye toward discerning the rationale for therapeutic targeting of DNA-PK. Significance: Although DNA-PK is classically considered a component of damage response, recent findings illuminate damage-independent functions of DNA-PK that affect multiple tumor-associated pathways and provide a rationale for the development of novel therapeutic strategies. (C) 2014 AACR.
引用
收藏
页码:1126 / 1139
页数:14
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