Chin Chur, Bae Jae Ho, Kim Mi Ju, Hwang Jee Young, Kim Su Jin, Yoon Man Soo, Lee Min Ki, Kim Dong Wan, Chung Byung Seon, Kang Chi Dug, Kim Sun Hee
Department of Biochemistry, Pusan National University Hospital, Busan 602-739, Korea.
Exp Mol Med. 2005 Dec 31;37(6):608-18. doi: 10.1038/emm.2005.74.
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.
在此,我们确定了在耐辐射的CEM/IR和FM3A/IR变体中哪些辐射反应基因发生了改变,这两种变体分别比亲代人白血病CEM细胞和小鼠乳腺癌FM3A细胞对辐射具有更高的抗性,并研究了放疗后观察到的辐射抗性是否可以通过抑制蛋白激酶A来恢复。与DNA损伤修复相关的DNA-PKcs、Ku70/80、Rad51和Rad54基因,以及与抗凋亡相关的Bcl-2和NF-κB基因的表达上调,但与亲代细胞相比,耐辐射细胞中促凋亡的Bax基因表达下调。我们还发现,对这些耐辐射细胞联合进行辐射和蛋白激酶A(PKA)抑制剂处理,会协同抑制细胞的DNA-PK、Rad51和Bcl-2表达,从而恢复细胞的辐射敏感性。我们的数据表明,放疗与PKA抑制剂联合治疗可能是一种针对耐辐射癌症的新型治疗策略。