PARP1 Expression in Pediatric Central Nervous System Tumors

被引:28
|
作者
Barton, Valerie N. [1 ,2 ]
Donson, Andrew M. [2 ]
Kleinschmidt-DeMasters, B. K. [3 ,4 ]
Gore, Lia [2 ]
Liu, Arthur K. [5 ]
Foreman, Nicholas K. [2 ]
机构
[1] Univ Colorado Denver, Hlth Sci Ctr, Dept Pediat, Aurora, CO 80045 USA
[2] Childrens Hosp Denver, Aurora, CO USA
[3] Univ Colorado Denver, Dept Neurosurg, Aurora, CO 80045 USA
[4] Univ Colorado Denver, Dept Pathol & Neurol, Aurora, CO 80045 USA
[5] Univ Colorado Denver, Dept Radiat Oncol, Aurora, CO 80045 USA
关键词
microarray; PARP1; inhibitor; pediatric brain tumor; POLY(ADP-RIBOSE) POLYMERASE-1 INHIBITOR; DNA-REPAIR; RIBOSYLATION;
D O I
10.1002/pbc.22141
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Despite advances in therapy, outcome in many high-grade pediatric central nervous system (CNS) tumors remains poor. The focus of neuro-oncology research has thus turned towards identifying novel therapeutic targets. Poly(ADP-ribose) polymerase-1 (PARP1) is a DNA repair protein that has been Studied in a variety of malignancies and may interfere with therapy-induced DNA damage, however expression in pediatric CNS tumors is unknown. Procedure. We evaluated PARP1 mRNA expression in 81 pediatric CNS tumors using microarray technology. Protein expression was examined by Western blot. Results. PARP1 mRNA is highly expressed in high-grade tumors (P < 0.0001). PARP1 mRNA expression was greater in high-grade glioma than pilocytic astrocytoma (P = 3.5 x 10(-5)) and in large cell medulloblastoma over classic medulloblastoma (P = 0.0053). PARP1 protein was also prominent in high-grade tumors (P = 0.022). Conclusion. These findings indicate that PARP1 is expressed ill high-grade pediatric CNS tumors, implicating PARP1 inhibition as a potential therapeutic target. Pediatr Blood Cancer 2009;53:1227-1230. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1227 / 1230
页数:4
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