4.2 Article

The pathological role and prognostic impact of miR-181 in acute myeloid leukemia

Journal

CANCER GENETICS
Volume 208, Issue 5, Pages 225-229

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cancergen.2014.12.006

Keywords

Acute myeloid leukemia; miR-181; diagnostic marker; prognostic predictor; tumor suppressor

Funding

  1. National Institutes of Health (NIH) [R01CA182528, R01CA127277, R01CA178454]
  2. American Cancer Society (ACS) Research Scholar grant [RSG-11-156-01-LIB]
  3. Leukemia & Lymphoma Society Translational Research grant
  4. Alex's Lemonade Stand Foundation for Childhood Cancer
  5. Spastic Paralysis Foundation of the Illinois, Eastern Iowa Branch of Kiwanis International

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In addition to genetic abnormalities, such as chromosomal translocations and somatic mutations that have been widely acknowledged in the leukemogenesis of acute myeloid leukemia (AML), epigenetic modifications also play a vital role in this process. MicroRNA (miRNA) regulation is emerging as a new layer of epigenetic regulation besides DNA methylation and histone modifications. Among the miRNAs first identified to be specifically expressed in hematopoietic cells, the miR-181 family has been implicated in regulating the differentiation of B cells, T cells, and natural killer cells during normal hematopoiesis, and has been linked tightly to the pathogenesis and prognosis of AML. Accumulating evidence indicates that miR-181 acts as a tumor suppressor in the pathogenesis of AML and exhibits a significant impact on the survival of patients with AML. Herein, we review the role of miR-181 as a diagnostic marker and prognostic predictor in AML, and discuss the potential use of miR-181 as a therapeutic target for AML.

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