TRANSFECTED MCF-7 CELLS AS A MODEL FOR BREAST-CANCER PROGRESSION

被引:44
作者
KERN, FG
MCLESKEY, SW
ZHANG, L
KUREBAYASHI, J
LIU, Y
DING, IYF
KHARBANDA, S
CHEN, D
MILLER, D
CULLEN, K
PAIK, S
DICKSON, RB
机构
[1] GEORGETOWN UNIV, SCH MED, WASHINGTON, DC 20007 USA
[2] GEORGETOWN UNIV, MED CTR, DEPT BIOCHEM & MOLEC BIOL, WASHINGTON, DC 20007 USA
[3] GEORGETOWN UNIV, MED CTR, DEPT PHARMACOL, WASHINGTON, DC 20007 USA
[4] GEORGETOWN UNIV, MED CTR, SCH NURSING, WASHINGTON, DC 20007 USA
[5] GEORGETOWN UNIV, MED CTR, DEPT MED, WASHINGTON, DC 20007 USA
[6] GEORGETOWN UNIV, MED CTR, DEPT PATHOL, WASHINGTON, DC 20007 USA
[7] GEORGETOWN UNIV, MED CTR, DEPT CELL BIOL & ANAT, WASHINGTON, DC 20007 USA
关键词
FIBROBLAST GROWTH FACTOR; GROWTH FACTOR RECEPTORS; C-ERB B-2; VASCULAR ENDOTHELIAL CELL GROWTH FACTOR; ANGIOGENESIS; METASTASIN; TAMOXIFEN SENSITIVITY;
D O I
10.1007/BF00666149
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The MCF-7 human breast carcinoma cell line has been used as a recipient for eukaryotic plasmid expression vectors to determine the effects of growth factor and growth factor receptor overexpression on the estrogen-dependent, antiestrogen sensitive and poorly metastatic phenotypes exhibited by this line. Overexpression of some members of the erbB family of ligands and receptors were found to have some effects on these phenotypes. However, only when two members of the fibroblast growth factor family, FGF-1 and FGF-4, were overexpressed was progressive in vivo growth observed is either ovariectomized nude mice without estrogen supplementation or in mice that received tamoxifen treatment. FGF transfected cells also exhibited an increased ability to form micrometastases. The implications of these results with regard to the possible role of the paracrine and autocrine effects of angiogenic growth factor production in breast cancer progression are discussed.
引用
收藏
页码:153 / 165
页数:13
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