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


ABSTRACT: RA-inducible gene I (RIG-I/DDX58) has been shown to activate IFN-? 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-? 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.

SUBMITTER: Jiang LJ 

PROVIDER: S-EPMC3033283 | biostudies-other | 2011 Feb

REPOSITORIES: biostudies-other

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

Jiang Lin-Jia LJ   Zhang Nan-Nan NN   Ding Fei F   Li Xian-Yang XY   Chen Lei L   Zhang Hong-Xin HX   Zhang Wu W   Chen Sai-Juan SJ   Wang Zhu-Gang ZG   Li Jun-Min JM   Chen Zhu Z   Zhu Jiang J  

Proceedings of the National Academy of Sciences of the United States of America 20110111 5


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  ...[more]

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