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ATDC/TRIM29 phosphorylation by ATM/MAPKAP kinase 2 mediates radioresistance in pancreatic cancer cells. | LitMetric

ATDC/TRIM29 phosphorylation by ATM/MAPKAP kinase 2 mediates radioresistance in pancreatic cancer cells.

Cancer Res

Authors' Affiliations: Departments of Surgery, Radiation Oncology, Pharmacology, Internal Medicine and Molecular and Integrative Physiology, Translational Oncology Program, and Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan.

Published: March 2014

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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961828PMC
http://dx.doi.org/10.1158/0008-5472.CAN-13-2289DOI Listing

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