Literature DB >> 22015065

miR-590-5p, miR-219-5p, miR-15b and miR-628-5p are commonly regulated by IL-3, GM-CSF and G-CSF in acute myeloid leukemia.

Amanda J Favreau1, Pradeep Sathyanarayana.   

Abstract

Aberrations in IL-3, GM-CSF and G-CSF induced signaling are frequently reported in acute myeloid leukemia (AML). Herein, we utilized a unique human myeloid leukemic cell line, AML-193, which responds to all three cytokines to analyze the regulation at microRNA level. Using real-time PCR-based miRNA expression profiling, we investigated miRNA signatures regulated by IL-3, GM-CSF and G-CSF for n=704 miRNAs. We discovered that in addition to regulating specific miRNAs, these cytokines also regulate common set of miRNAs, which includes miR-590-5p, miR-219-5p, miR-15b and miR-628-5p. Taken together, we have identified novel candidate miRNAs that may be instructive during leukemic and normal hematopoiesis.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22015065      PMCID: PMC3264807          DOI: 10.1016/j.leukres.2011.09.027

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  62 in total

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5.  The STAT5 inhibitor pimozide decreases survival of chronic myelogenous leukemia cells resistant to kinase inhibitors.

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  19 in total

1.  Youth and environmental enrichment generate serum exosomes containing miR-219 that promote CNS myelination.

Authors:  Aya D Pusic; Richard P Kraig
Journal:  Glia       Date:  2013-12-04       Impact factor: 7.452

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4.  Survival of autoreactive T lymphocytes by microRNA-mediated regulation of apoptosis through TRAIL and Fas in type 1 diabetes.

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5.  Circulatory miR-628-5p is downregulated in prostate cancer patients.

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Review 6.  Aberrant regulation of miR-15b in human malignant tumors and its effects on the hallmarks of cancer.

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7.  MicroRNA Regulating Glutathione S-Transferase P1 in Prostate Cancer.

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8.  A miR-590/Acvr2a/Rad51b axis regulates DNA damage repair during mESC proliferation.

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10.  Walking the interactome to identify human miRNA-disease associations through the functional link between miRNA targets and disease genes.

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