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

被引:27
作者
Chin, C
Bae, JH
Kim, MJ
Hwang, JY
Kim, SJ
Yoon, MS
Lee, MK
Kim, DW
Chung, BS
Kang, CD
Kim, SH [1 ]
机构
[1] Pusan Natl Univ, Dept Biochem, Pusan 609735, South Korea
[2] Pusan Natl Univ, Res Ctr Ischem Tissue Regenerat, Coll Med, Pusan 609735, South Korea
[3] Pusan Natl Univ Hosp, Med Res Inst, Pusan 602739, South Korea
[4] Pusan Natl Univ Hosp, Canc Res Ctr, Pusan 602739, South Korea
[5] Chang Won Natl Univ, Dept Microbiol, Coll Nat Sci, Chang Won 641773, South Korea
关键词
cyclic AMP-dependent protein kinases; gene expression profiling; gene expression regulation; neoplastic; radiation;
D O I
10.1038/emm.2005.74
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here we determined which radiation-responsive genes were altered in radioresistant CEM/IR and FM3A/lR 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-kappa B 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.
引用
收藏
页码:608 / 618
页数:11
相关论文
共 39 条
[1]   The radioprotective effect of the 24 kDa FGF-2 isoform in HeLa cells is related to an increased expression and activity of the DNA dependent protein kinase (DNA-PK) catalytic subunit [J].
Ader, I ;
Muller, C ;
Bonnet, J ;
Favre, G ;
Cohen-Jonathan, E ;
Salles, B ;
Toulas, C .
ONCOGENE, 2002, 21 (42) :6471-6479
[2]  
Allen C, 2003, MOL CANCER RES, V1, P913
[3]   Activation of stress-responsive promoters by ionizing radiation for deployment in targeted gene therapy [J].
Chastel, C ;
Jiricny, J ;
Jaussi, R .
DNA REPAIR, 2004, 3 (03) :201-215
[4]  
CHEN X, 2005, CANCER RES, V62, P1213
[5]   Overexpression of Bcl-2 in squamous cell carcinoma of the larynx: A marker of radioresistance [J].
Condon, LT ;
Ashman, JNE ;
Ell, SR ;
Stafford, ND ;
Greenman, J ;
Cawkwell, L .
INTERNATIONAL JOURNAL OF CANCER, 2002, 100 (04) :472-475
[6]   Role of chemopreventive agents in cancer therapy [J].
Dorai, T ;
Aggarwal, BB .
CANCER LETTERS, 2004, 215 (02) :129-140
[7]   Homologous and non-homologous recombination differentially affect DNA damage repair in mice [J].
Essers, J ;
van Steeg, H ;
de Wit, J ;
Swagemakers, SMA ;
Vermeij, M ;
Hoeijmakers, JHJ ;
Kanaar, R .
EMBO JOURNAL, 2000, 19 (07) :1703-1710
[8]   PROTEIN KINASE-A INHIBITORS ENHANCE RADIATION-INDUCED APOPTOSIS [J].
FINDIK, D ;
SONG, QZ ;
HIDAKA, H ;
LAVIN, M .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, 57 (01) :12-21
[9]   Differential gene expression profiles of radioresistant oesophageal cancer cell lines established by continuous fractionated irradiation [J].
Fukuda, K ;
Sakakura, C ;
Miyagawa, K ;
Kuriu, Y ;
Kin, S ;
Nakase, Y ;
Hagiwara, A ;
Mitsufuji, S ;
Okazaki, Y ;
Hayashizaki, Y ;
Yamagishi, H .
BRITISH JOURNAL OF CANCER, 2004, 91 (08) :1543-1550
[10]   Genetic analysis of the DNA-dependent protein kinase reveals an inhibitory role of Ku in late S-G2 phase DNA double-strand break repair [J].
Fukushima, T ;
Takata, M ;
Morrison, C ;
Araki, R ;
Fujimori, A ;
Abe, M ;
Tatsumi, K ;
Jasin, M ;
Dhar, PK ;
Sonoda, E ;
Chiba, T ;
Takeda, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (48) :44413-44418