抗辐射性
癌症研究
DNA损伤
胰腺癌
磷酸化
DNA修复
激酶
催化亚单位
生物
癌症
化学
细胞生物学
蛋白激酶A
DNA
细胞培养
遗传学
作者
Lidong Wang,Huibin Yang,Phillip L. Palmbos,Gina M. Ney,Taylor Detzler,Dawn M. Coleman,Jacob Leflein,Mary A. Davis,Min Zhang,Wenhua Tang,J. Kevin Hicks,Corey M. Helchowski,Jayendra Prasad,Theodore S. Lawrence,Liang Xu,Xiaochun Yu,Christine E. Canman,Mats Ljungman,Diane M. Simeone
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2014-01-28
卷期号:74 (6): 1778-1788
被引量:57
标识
DOI:10.1158/0008-5472.can-13-2289
摘要
Pancreatic ductal adenocarcinoma (PDAC) is characterized by therapeutic resistance for which the basis is poorly understood. Here, we report that the DNA and p53-binding protein ATDC/TRIM29, which is highly expressed in PDAC, plays a critical role in DNA damage signaling and radioresistance in pancreatic cancer cells. Ataxia-telangiectasia group D-associated gene (ATDC) mediated resistance to ionizing radiation in vitro and in vivo in mouse xenograft assays. ATDC was phosphorylated directly by MAPKAP kinase 2 (MK2) at Ser550 in an ATM-dependent manner. Phosphorylation at Ser-550 by MK2 was required for the radioprotective function of ATDC. Our results identify a DNA repair pathway leading from MK2 and ATM to ATDC, suggesting its candidacy as a therapeutic target to radiosensitize PDAC and improve the efficacy of DNA-damaging treatment.
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