Article

Radiosensitization by targeting radioresistance-related genes with protein kinase A inhibitor in radioresistant cancer cells.

Department of Biochemistry, Pusan National University Hospital, Busan 602-739, Korea.
Experimental and Molecular Medicine (impact factor: 2.48). 01/2006; 37(6):608-18. pp.608-18
Source: PubMed

ABSTRACT Here we determined which radiation-responsive genes were altered in radioresistant CEM/IR and FM3A/IR variants, which showed higher resistance to irradiation than parental human leukemia CEM and mouse mammary carcinoma FM3A cells, respectively and studied if radioresistance observed after radiotherapy could be restored by inhibition of protein kinase A. The expressions of DNA-PKcs, Ku70/80, Rad51 and Rad54 genes that related to DNA damage repair, and Bcl-2 and NF-kappaB genes that related to antiapoptosis, were up-regulated, but the expression of proapototic Bax gene was down-regulated in the radioresistant cells as compared to each parental counterpart. We also revealed that the combined treatment of radiation and the inhibitor of protein kinase A (PKA) to these radioresistant cells resulted in synergistic inhibition of DNA-PK, Rad51 and Bcl-2 expressions of the cells, and consequently restored radiosensitivity of the cells. Our results propose that combined treatment with radiotherapy and PKA inhibitor can be a novel therapeutic strategy to radioresistant cancers.

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Keywords

antiapoptosis
 
DNA damage
 
mouse mammary carcinoma FM3A cells
 
NF-kappaB genes
 
novel therapeutic strategy
 
parental counterpart
 
parental human leukemia CEM
 
PKA
 
PKA inhibitor
 
proapototic Bax gene
 
protein kinase A
 
Rad54 genes
 
radiation-responsive genes
 
radioresistance
 
radioresistant cancers
 
radioresistant cells
 
radioresistant CEM/IR
 
radiosensitivity
 
radiotherapy
 
showed higher resistance