CYCLOSPORINE-A INHIBITS GROWTH OF AUTOCRINE TUMOR-CELL LINES BY DESTABILIZING INTERLEUKIN-3 MESSENGER-RNA

被引:107
作者
NAIR, APK
HAHN, S
BANHOLZER, R
HIRSCH, HH
MORONI, C
机构
[1] Institute for Medical Microbiology, University of Basel, CH-4003 Basel
关键词
D O I
10.1038/369239a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
IN T cells, cyclosporin A (CsA) exerts its immunosuppressive effect by preventing transcriptional induction of the expression of interleukin(IL)-2. This is achieved by a mechanism that involves binding of a CsA-cyclophilin complex to calcineurin, which in turn inhibits the phosphatase-controlled translocation of transcription factor NFAT to the nucleus(1-8). We have previously identified IL-3 as an autocrine oncogenic regulator in tumour cell lines generated by introducing the v-H-ras oncogene into IL-3-dependent mast cells(9-12). Here we report that CsA specifically blocks autocrine tumour cell growth. The mechanism involves down-regulation of IL-3 expression by destabilization of the messenger RNA and requires ongoing transcription. Transcripts from exogenous IL-3 genes lacking the (A + U)-rich element (ARE) in the 3' untranslated terminal repeat could not be destabilized, suggesting that at least part of this sequence, which is known to mediate decay of short-lived mRNA(13), participates in a CsA-sensitive regulatory mechanism.
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页码:239 / 242
页数:4
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