RA-inducible gene-I induction augments STAT1 activation to inhibit leukemia cell proliferation.
basic_science · Level V
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- Record sourced from PubMed, PMID 21224412.
- Also identified by DOI 10.1073/pnas.1019059108 and PMC identifier 3033283.
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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.
Medical subject headings
- Cell Proliferation
- DEAD-box RNA Helicases
- Leukemia
- STAT1 Transcription Factor