Impaired expression of a human septin family gene Bradeion inhibits the growth and tumorigenesis of colorectal cancer in vitro and in vivo

被引:27
作者
Tanaka, M
Kijima, H
Itoh, J
Matsuda, T
Tanaka, T
机构
[1] Natl Inst Adv Ind Sci & Technol, Dept Collaborat, Tsukuba, Ibaraki 3058566, Japan
[2] Tokai Univ, Sch Med, Isehara, Kanagawa 2591193, Japan
关键词
Bradeion; septin family genes; cytokinesis; antisense ribozyme; G2; arrest;
D O I
10.1038/sj.cgt.7700460
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have identified a novel human septin family gene Bradeion, which is specifically expressed in human colorectal cancer and malignant melanoma. In order to analyze the implications of tumor-specific gene expression, ribozymes and its derivatives were specifically designed and transfected into various colorectal adenocarcinoma cell lines for Bradeion inactivation. We constructed ribozyme expression plasmids controlled by a human tRNA(Val) promoter, and both hammerhead ribozyme and its allosteric derivative maxizyme were used for two different forms of Bradeion mRNA. The sequence-specific cleavage of Bradeion mRNA resulted in significant growth inhibition and G2 arrest in human cancer cell lines, detected by flow cytometry analysis. In addition, in vivo mice studies demonstrated marked tumor growth suppression by the Bradeion-specific ribozymes. Thus, the tumor-specific and selective marker Bradeion also provides valuable tools as a potential target for colorectal cancer therapy.
引用
收藏
页码:483 / 488
页数:6
相关论文
共 18 条
[1]   RAS GENES [J].
BARBACID, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :779-827
[2]  
BOS JL, 1989, CANCER RES, V49, P4682
[3]   Requirement for p53 and p21 to sustain G2 arrest after DNA damage [J].
Bunz, F ;
Dutriaux, A ;
Lengauer, C ;
Waldman, T ;
Zhou, S ;
Brown, JP ;
Sedivy, JM ;
Kinzler, KW ;
Vogelstein, B .
SCIENCE, 1998, 282 (5393) :1497-1501
[4]   ACTIVATION OF KI-RAS 2 GENE IN HUMAN-COLON AND LUNG CARCINOMAS BY 2 DIFFERENT POINT MUTATIONS [J].
CAPON, DJ ;
SEEBURG, PH ;
MCGRATH, JP ;
HAYFLICK, JS ;
EDMAN, U ;
LEVINSON, AD ;
GOEDDEL, DV .
NATURE, 1983, 304 (5926) :507-513
[5]   Distinct roles of the co-activators p300 and CBP in retinoic-acid-induced F9-cell differentiation [J].
Kawasaki, H ;
Eckner, R ;
Yao, TP ;
Taira, K ;
Chiu, R ;
Livingston, DM ;
Yokoyama, KK .
NATURE, 1998, 393 (6682) :284-289
[6]   Therapeutic applications of ribozymes [J].
Kijima, H ;
Ishida, H ;
Ohkawa, T ;
KashaniSabet, M ;
Scanlon, KJ .
PHARMACOLOGY & THERAPEUTICS, 1995, 68 (02) :247-267
[7]  
KUWABATA T, 1999, P NATL ACAD SCI USA, V95, P1886
[8]   A novel mitochondrial septin-like protein, ARTS, mediates apoptosis dependent on its P-loop motif [J].
Larisch, S ;
Yi, YS ;
Lotan, R ;
Kerner, H ;
Eimerl, S ;
Parks, WT ;
Gottfried, Y ;
Reffey, SB ;
de Caestecker, MP ;
Danielpour, D ;
Book-Melamed, N ;
Timberg, R ;
Duckett, CS ;
Lechleider, RJ ;
Steller, H ;
Orly, J ;
Kim, SJ ;
Roberts, AB .
NATURE CELL BIOLOGY, 2000, 2 (12) :915-921
[9]  
LEIBOVITZ A, 1976, CANCER RES, V36, P4562
[10]   The septins: Roles in cytokinesis and other processes [J].
Longtine, MS ;
DeMarini, DJ ;
Valencik, ML ;
AlAwar, OS ;
Fares, H ;
DeVirgilio, C ;
Pringle, JR .
CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (01) :106-119