RA-inducible gene-I induction augments STAT1 activation to inhibit leukemia cell proliferation

Proc Natl Acad Sci U S A. 2011 Feb 1;108(5):1897-902. doi: 10.1073/pnas.1019059108. Epub 2011 Jan 11.

Abstract

RA-inducible gene I (RIG-I/DDX58) has been shown to activate IFN-β promoter stimulator 1 (IPS-1) on recognizing cytoplasmic viral RNAs. It is unclear how RIG-I functions within the IFN and/or RA signaling process in acute myeloid leukemia (AML) cells, however, where obvious RIG-I induction is observed. Here, we show that the RIG-I induction functionally contributes to IFN-α plus RA-triggered growth inhibition of AML cells. Interestingly, although RIG-I induction itself is under the regulation of STAT1, a major IFN intracellular signal mediator, under circumstances in which it does not stimulate IPS-1, it conversely augments STAT1 activation to induce IFN-stimulatory gene expression and inhibit leukemia cell proliferation. Thus, our results unveil a previously undescribed RIG-I activity in regulating the cellular proliferation of leukemia cells via STAT1, which is independent of its classic role of sensing viral invasion to trigger type I IFN transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation*
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases / genetics*
  • Gene Expression Regulation / drug effects
  • Humans
  • Leukemia / pathology*
  • Receptors, Immunologic
  • STAT1 Transcription Factor / metabolism*
  • Tretinoin / pharmacology
  • U937 Cells

Substances

  • Receptors, Immunologic
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Tretinoin
  • RIGI protein, human
  • DEAD Box Protein 58
  • DEAD-box RNA Helicases