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Beyond DNA Repair: DNA-PK Function in Cancer
被引:193
|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.
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页码:1126 / 1139
页数:14
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