Inhibition of Wilms' tumor growth by intramuscular administration of tissue inhibitor of metalloproteinases-4 plasmid DNA

被引:52
作者
Çeliker, MY
Wang, M
Atsidaftos, E
Liu, X
Liu, YE
Jiang, Y
Valderrama, E
Goldberg, ID
Shi, YE
机构
[1] Long Isl Jewish Med Ctr, Dept Radiat Oncol, New Hyde Park, NY 11040 USA
[2] Schneider Childrens Hosp, Long Isl Jewish Med Ctr, Div Pediat Hematol Oncol, New Hyde Park, NY 11040 USA
[3] Long Isl Jewish Med Ctr, Dept Med, New Hyde Park, NY 11040 USA
[4] Long Isl Jewish Med Ctr, Dept Radiat Oncol, New Hyde Park, NY 11040 USA
[5] Long Isl Jewish Med Ctr, Dept Pathol, New Hyde Park, NY 11040 USA
关键词
TIMP-4; Wilms' tumor; gene therapy; growth inhibition; tumorigenesis;
D O I
10.1038/sj.onc.1204508
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
Extracellular matrix (ECM) degrading matrix metalloproteinases (MMPs) lead to ECM turnover, a key event in cancer growth and progression. The tissue inhibitors of matrix metalloproteinases (TIMPs) Limit the activity of MMPs, which suggests their use for cancer gene therapy. Here we report that systemic administration of naked TIMP-4 DNA significantly inhibited Wilms' tumor growth in nude mice. TIMP-4, whose expression was lost in Wilms' tumor, inhibited the growth of G401 Wilms' tumor tells at a concentration lower than those required for MMP inhibition. This inhibition was associated with internalization of exogenous recombinant TIMP-4, Electroporation-mediated intramuscular injection of TIMP-4 expression plasmid resulted in sustained plasma TIMP-4 levels and significant tumor suppression. Our data demonstrate a tumor suppressive effect of TIMP-4 against Wilms' tumor and the potential utility of intramuscular delivery of TIMP gene for treatment of kidney derived cancers.
引用
收藏
页码:4337 / 4343
页数:7
相关论文
共 34 条
[1]   Gene transfer into muscle by electroporation in vivo [J].
Aihara, H ;
Miyazaki, J .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :867-870
[2]  
BACCALAO R, 1995, HDB BIOL CONFOCAL MI, P311
[3]   Divergent effects of tissue inhibitor of metalloproteinase-1, -2, or -3 overexpression on rat vascular smooth muscle cell invasion, proliferation, and death in vitro - TIMP-3 promotes apoptosis [J].
Baker, AH ;
Zaltsman, AB ;
George, SJ ;
Newby, AC .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (06) :1478-1487
[4]   A NOVEL METALLOPROTEINASE GENE SPECIFICALLY EXPRESSED IN STROMAL CELLS OF BREAST CARCINOMAS [J].
BASSET, P ;
BELLOCQ, JP ;
WOLF, C ;
STOLL, I ;
HUTIN, P ;
LIMACHER, JM ;
PODHAJCER, OL ;
CHENARD, MP ;
RIO, MC ;
CHAMBON, P .
NATURE, 1990, 348 (6303) :699-704
[5]   DIRECT EVIDENCE LINKING EXPRESSION OF MATRIX METALLOPROTEINASE-9 (92-KDA GELATINASE/COLLAGENASE) TO THE METASTATIC PHENOTYPE IN TRANSFORMED RAT EMBRYO CELLS [J].
BERNHARD, EJ ;
GRUBER, SB ;
MUSCHEL, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4293-4297
[6]   GROWTH-STIMULATION OF HUMAN KERATINOCYTES BY TISSUE INHIBITOR OF METALLOPROTEINASES [J].
BERTAUX, B ;
HORNEBECK, W ;
EISEN, AZ ;
DUBERTRET, L .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (04) :679-685
[7]   Suppression of in vivo tumor growth and induction of suspension cell death by tissue inhibitor of metalloproteinases (TIMP)-3 [J].
Bian, JH ;
Wang, YL ;
Smith, MR ;
Kim, H ;
Jacobs, C ;
Jackman, J ;
Kung, HF ;
Colburn, NH ;
Sun, Y .
CARCINOGENESIS, 1996, 17 (09) :1805-1811
[8]   Specific, high affinity binding of tissue inhibitor of metalloproteinases-4 (TIMP4) to the COOH-terminal hemopexin-like domain of human gelatinase A - TIMP-4 binds progelatinase A and the COOH-terminal domain in a similar manner to TIMP-2 [J].
Bigg, HF ;
Shi, YE ;
Liu, YLE ;
Steffensen, B ;
Overall, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (24) :15496-15500
[9]   Systemic inhibition of tumor growth and tumor metastases by intramuscular administration of the endostatin gene [J].
Blezinger, P ;
Wang, JJ ;
Gondo, M ;
Quezada, A ;
Mehrens, D ;
French, M ;
Singhal, A ;
Sullivan, S ;
Rolland, A ;
Ralston, R ;
Min, W .
NATURE BIOTECHNOLOGY, 1999, 17 (04) :343-348
[10]   The TIMP2 membrane type 1 metalloproteinase "receptor" regulates the concentration and efficient activation of progelatinase A - A kinetic study [J].
Butler, GS ;
Butler, MJ ;
Atkinson, SJ ;
Will, H ;
Tamura, T ;
van Westrum, SS ;
Crabbe, T ;
Clements, J ;
d'Ortho, MP ;
Murphy, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (02) :871-880