SODIUM-BUTYRATE INHIBITS EXPRESSION OF UROKINASE AND ITS RECEPTOR MESSENGER-RNAS AT BOTH TRANSCRIPTION AND POST-TRANSCRIPTION LEVELS IN COLON-CANCER CELLS

被引:24
作者
DANG, JJ [1 ]
WANG, Y [1 ]
DOE, WF [1 ]
机构
[1] AUSTRALIAN NATL UNIV,JOHN CURTIN SCH MED RES,DIV CLIN SCI,CANBERRA,ACT 2601,AUSTRALIA
关键词
BUTYRATE; UROKINASE; UROKINASE RECEPTOR; TUMOR NECROSIS FACTOR;
D O I
10.1016/0014-5793(95)00029-9
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
The effects of butyrate on the modulation of urokinase plasminogen activator (uPA) and its receptor (uPAR) mRNAs were studied, While both mRNA levels were increased after stimulation by tumor necrosis factor alpha (TNF alpha), phorbol ester (PMA) and cycloheximide, they were inhibited by butyrate at 2.5 to 25 mM. Nuclear run-on transcription assays indicated that uPA mRNA was modulated by butyrate at the transcriptional level but the uPAR gene was regulated at both transcriptional and post-transcriptional levels in the presence or absence of TNF alpha. In the presence of PMA, however, butyrate acts at the posttranscriptional level on both genes.
引用
收藏
页码:147 / 150
页数:4
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