Downregulation of survivin expression by induction of the effector cell protease receptor-1 reduces tumor growth potential and results in an increased sensitivity to anticancer agents in human colon cancer

被引:66
作者
Yamamoto, T
Manome, Y
Nakamura, M
Tanigawa, N
机构
[1] Osaka Med Coll, Dept Gen & Gastroenterol Surg, Takatsuki, Osaka 5698686, Japan
[2] Jikei Univ, Sch Med, Dept Microbiol, Minato Ku, Tokyo 1050003, Japan
关键词
survivin; effector cell protease receptor-1; 5-fluorouracil; cisplatin; colon carcinoma;
D O I
10.1016/S0959-8049(02)00247-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Survivin, a novel inhibitor of apoptosis, is expressed in cancer cells and not in normal adult tissues, and is recognised as a potential target in anticancer therapy. The induction of a natural antisense of survivin, effector cell protease receptor-1 (EPR-1), in a human colon cancer cell line resulted in a downregulation of survivin expression, with a similar decrease in cell proliferation, an increase in apoptosis and an increase in the sensitivity to anticancer agents. In addition, subcutaneous (s.c.) tumours from EPR-1 transfectants showed a significant reduction in size compared with parental cells, and this antitumour efficacy was further enhanced in combination with anticancer agents. These findings suggest that regulation of survivin by the induction of EPR-1 cDNA may have significant potential as a therapy for human colon cancer. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2316 / 2324
页数:9
相关论文
共 30 条
[1]   Anti-apoptosis gene, survivin, and prognosis of neuroblastoma [J].
Adida, C ;
Berrebi, D ;
Peuchmaur, M ;
Reyes-Mugica, M ;
Altieri, DC .
LANCET, 1998, 351 (9106) :882-883
[2]  
Adida C, 1998, AM J PATHOL, V152, P43
[3]   XA RECEPTOR EPR-1 [J].
ALTIERI, DC .
FASEB JOURNAL, 1995, 9 (10) :860-865
[4]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[5]   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
[6]   Survivin as a radioresistance factor in pancreatic cancer [J].
Asanuma, K ;
Moriai, R ;
Yajima, T ;
Yagihashi, A ;
Yamada, M ;
Kobayashi, D ;
Watanabe, N .
JAPANESE JOURNAL OF CANCER RESEARCH, 2000, 91 (11) :1204-1209
[7]   GROWTH-FACTORS IN DEVELOPMENT, TRANSFORMATION, AND TUMORIGENESIS [J].
CROSS, M ;
DEXTER, TM .
CELL, 1991, 64 (02) :271-280
[8]   A conserved family of cellular genes related to the baculovirus iap gene and encoding apoptosis inhibitors [J].
Duckett, CS ;
Nava, VE ;
Gedrich, RW ;
Clem, RJ ;
VanDongen, JL ;
Gilfillan, MC ;
Shiels, H ;
Hardwick, JM ;
Thompson, CB .
EMBO JOURNAL, 1996, 15 (11) :2685-2694
[9]  
Grossman D, 1999, LAB INVEST, V79, P1121
[10]   Inhibition of melanoma tumor growth in vivo by survivin targeting [J].
Grossman, D ;
Kim, PJ ;
Schechner, JS ;
Altieri, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :635-640