INHIBITION OF COLLAGENOLYTIC ACTIVITY IN HUMAN LEUKEMIC K562-CELLS BY TAMOXIFEN

被引:4
作者
AKELI, MG
MADOULET, C
RALLET, A
JARDILLIER, JC
机构
[1] FAC PHARM REIMS, BIOCHIM LAB, ETUD INTERACT BIOL SUBSTANCES ANTICANC GRP, 51 RUE COGNACQ JAY, F-51096 REIMS, FRANCE
[2] INST JEAN GODINOT, BIOCHIM LAB, F-51056 REIMS, FRANCE
关键词
COLLAGENOLYTIC ACTIVITY; K562; CELLS; PLASMINOGEN ACTIVATOR; TAMOXIFEN; CANCER;
D O I
10.1016/0145-2126(91)90184-U
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Presence of a collagenolytic activity has been demonstrated in the human leukemic cell line K562. Among various effectors studied, tamoxifen, a well-known antiestrogenic compound, exhibited a strong inhibitory effect. After 3 days of culture in the presence of 10(-7) M of tamoxifen, 75% of the collagenolytic activity was inhibited. Hydroxytamoxifen and N-desmethyltamoxifen were equally potent inhibitors though devoid of the direct cytotoxic effect. Cis-tamoxifen was less efficient. K562 cells have no binding sites for estrogens but they possess high affinity binding sites for H-3-tamoxifen (295 fmol/mg of proteins, K(D) = 0.25 x 10(-9) M). Tamoxifen had no effect on cellular differentiation or enzyme secretion. Anticollagenolytic activity of tamoxifen (10(-7)-10(-6) M) could be related to its inhibitory action on plasmin and plasminogen activator.
引用
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页码:1153 / 1157
页数:5
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