EFFECTS OF IFN-BETA ON GROWTH OF HUMAN PROSTATIC JCA-1 CALLS

被引:9
作者
NAKAJIMA, Y
KONNO, S
PERRUCCIO, L
CHEN, Y
WU, JM
AN, S
CHIAO, J
CHOUDHURY, M
MALLOUH, C
MURAKI, J
机构
[1] NEW YORK MED COLL,DEPT BIOCHEM & MOLEC BIOL,VALHALLA,NY 10595
[2] NEW YORK MED COLL,DEPT MED,VALHALLA,NY 10595
[3] NEW YORK MED COLL,DEPT UROL,VALHALLA,NY 10595
[4] TOCHIGI CANC CTR,TOCHIGI,JAPAN
关键词
D O I
10.1006/bbrc.1994.1472
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
Addition of IFN-beta resulted in a dose-dependent reduction of growth, a drop in [H-3] thymidine incorporation into DNA, and a concurrent 69% and 15% increase in the S and G(2)/M phases, of the human prostatic JCA-1 cells. No correlation existed between the antimitogenicity of IFN and increases in the double-stranded RNA dependent protein kinase activity. Although IFN elicited a large increase in 2-5A synthetase activity, activation of the 2-5A-dependent RNase L could not be demonstrated in JCA-1 cells rendered permeable to 2-5A, implying that the 2-5A pathway is not involved in the anti-proliferative effects of IFN. Analysis of endogenous proteins phosphorylated in vitro show that some IFN-inducible phosphoproteins were dependent upon the presence of double-stranded DNA. (C) 1994 Academic Press, Inc.
引用
收藏
页码:467 / 474
页数:8
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