Inhibition of tumor growth and metastasis of human breast cancer cells transfected with tissue inhibitor of metalloproteinase 4

被引:132
作者
Wang, MS
Liu, YLE
Greene, J
Sheng, SJ
Fuchs, A
Rosen, EM
Shi, YE
机构
[1] LONG ISL JEWISH MED CTR,ALBERT EINSTEIN COLL MED,DEPT PEDIAT,NEW HYDE PK,NY 11040
[2] LONG ISL JEWISH MED CTR,ALBERT EINSTEIN COLL MED,DEPT PATHOL,NEW HYDE PK,NY 11040
[3] LONG ISL JEWISH MED CTR,ALBERT EINSTEIN COLL MED,DEPT RADIAT ONCOL,NEW HYDE PK,NY 11040
[4] HUMAN GENOME SCI INC,ROCKVILLE,MD 20850
[5] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV CANC GENET,BOSTON,MA 02115
关键词
TIMP; MMP; mammary carcinoma; nude mice; angiogenesis;
D O I
10.1038/sj.onc.1201245
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
We recently identified, cloned, and characterized a novel human tissue inhibitor of metalloproteinases-4, TIMP-4 (Greene et al., 1996), To determine if TIMP-4 can modulate the in vivo growth of human breast cancers, Ne transfected a full-length TIMP-4 cDNA into MDA-MB-435 human breast cancer cells and studied the orthotopic growth of TIMP-4-transfected (TIMP4-435) versus control (neo-435) clones in the mammary fat pad of athymic nude mice, TIMP4-435 clones expressed TIMP-4 mRNA and produced anti-metalloproteinase (MMP) activity, while neo-435 clones did not express TIMP-4 mRNA or produce detectable anti-MMP activity. Overexpression of TIMP-4 inhibited the invasion potential of the cells in the in vitro invasion assay, When injected orthotopically into nude mice, TIMP-4 transfectants were significantly inhibited in tumor growth by 4-10-fold in primary tumor volumes; and in an axillary lymph node and lung metastasis as compared with controls. These results suggest the therapeutic potential of TIMP-4 in treating cancer malignant progression.
引用
收藏
页码:2767 / 2774
页数:8
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