Chemosensitization of bladder cancer cells by survivin-directed antisense oligodeoxynucleotides and siRNA

被引:45
作者
Fuessel, S
Herrmann, J
Ning, SL
Kotzsch, M
Kraemer, K
Schmidt, U
Hakenberg, OW
Wirth, MP
Meye, A
机构
[1] Tech Univ Dresden, Dept Urol, D-01307 Dresden, Germany
[2] Tech Univ Dresden, Inst Pathol, D-01307 Dresden, Germany
关键词
antisense oligodeoxnucleotides; bladder cancer; chemosensitization; siRNA; survivin;
D O I
10.1016/j.canlet.2005.02.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Survivin is known to be overexpressed in numerous tumor types including human bladder cancer and to cause resistance to radiation and chemotherapy. Therefore, we tested the antisense oligodeoxynucleotide AS-SVV286 and the small interfering RNA si-SVV284 to down-regulate survivin in the BCa cell lines EJ28 and 5637 thereby acting as sensitizers for chemotherapy. Pretreatment with these inhibitors followed by chemotherapy caused in enhanced decrease in cell viability. The observed reduction in Cell Counts associated with increased rates of apoptosis paralleled the degree of reduction of survivin expression that was achieved more efficiently by the siRNA than by the AS-ODN. Nevertheless, both therapy approaches in combination with all tested chemotherapeutics provoked a remarkable inhibition of viability and may serve as Suitable additive tools for chemosensitization of bladder cancer cells. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:243 / 254
页数:12
相关论文
共 64 条
[1]   Molecular circuits of apoptosis regulation and cell division control: The survivin paradigm [J].
Altieri, DC .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 92 (04) :656-663
[2]  
ALTIERI DC, 2001, NAT REV CANCER, V3, P46
[3]   Induction of apoptosis and inhibition of cell proliferation by survivin gene targeting [J].
Ambrosini, G ;
Adida, C ;
Sirugo, G ;
Altieri, DC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (18) :11177-11182
[4]   Acute ablation of survivin uncovers p53-dependent mitotic checkpoint functions and control of mitochondrial apoptosis [J].
Beltrami, E ;
Plescia, J ;
Wilkinson, JC ;
Duckett, CS ;
Altieri, DC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (03) :2077-2084
[5]   Inhibition of potentially anti-apoptotic proteins by antisense protein kinase C-α (Isis 3521) and antisense bcl-2 (G3139) phosphorothioate oligodeoxynucleotides:: Relationship to the decreased viability of T24 bladder and PC3 prostate cancer cells [J].
Benimetskaya, L ;
Miller, P ;
Benimetsky, S ;
Maciaszek, A ;
Guga, P ;
Beaucage, SL ;
Wilk, A ;
Grajkowski, A ;
Halperin, AL ;
Stein, CA .
MOLECULAR PHARMACOLOGY, 2001, 60 (06) :1296-1307
[6]   Comparison of antisense oligonucleotides and siRNAs in cell culture and in vivo [J].
Bertrand, JR ;
Pottier, M ;
Vekris, A ;
Opolon, P ;
Maksimenko, A ;
Malvy, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 296 (04) :1000-1004
[7]   Caspase involved synergistic cytotoxicity of bcl-2 antisense oligonucleotides and Adriamycin on transitional cell cancer cells [J].
Bilim, V ;
Kasahara, T ;
Noboru, H ;
Takahashi, K ;
Tomita, Y .
CANCER LETTERS, 2000, 155 (02) :191-198
[8]  
Böhle A, 2004, UROLOGY, V63, P682, DOI 10.1016/j.urology.2003.11.049
[9]   XIAP and survivin as therapeutic targets for radiation sensitization in preclinical models of lung cancer [J].
Cao, C ;
Mu, Y ;
Hallahan, DE ;
Lu, B .
ONCOGENE, 2004, 23 (42) :7047-7052
[10]   Survivin is required for stable checkpoint activation in taxol-treated HeLa cells [J].
Carvalho, A ;
Carmena, M ;
Sambade, C ;
Earnshaw, WC ;
Wheatley, SP .
JOURNAL OF CELL SCIENCE, 2003, 116 (14) :2987-2998