Cohesin mutations in myeloid malignancies made simple Journal Article


Authors: Viny, A. D.; Levine, R. L.
Article Title: Cohesin mutations in myeloid malignancies made simple
Abstract: Purpose of review Recurrent loss of function mutations within genes of the cohesin complex have been identified in myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). STAG2 is the most commonly mutated cohesin member in AML as well as solid tumors. STAG2 is recurrently, mutated in Ewing's Sarcoma, bladder cancer, and glioblastoma, and is one of only ten genes known to be recurrently mutated in over four distinct tissue types of human cancer Recent findings The cohesin complex, a multiprotein ring, is canonically known to align and stabilize replicated chromosomes prior to cell division. Although initially thought to lead to unequal chromosomal separation in dividing cells, data in myeloid malignancies show this is not observed in cohesin mutant MDS/AML, either in large patient cohorts or mouse models. Mounting evidence supports a potential alternate mechanism whereby drivers of cell-type specific gene expression and hematopoietic development are impaired through alteration in three-dimensional nuclear organization and gene structure. Summary Understanding the functional consequences of cohesin mutations in regulating lineage-specific and signal-dependent defects and in myeloid transformation will identify novel pathophysiologic mechanisms of disease and inform the development of novel therapeutic targets. © 2018 Wolters Kluwer Health, Inc. All rights reserved.
Keywords: leukemia; unclassified drug; gene mutation; review; nonhuman; pathophysiology; cohesin; incidence; protein; myelodysplastic syndrome; transcription; aneuploidy; acute myeloid leukemia; myeloid; human; priority journal; stag2 protein
Journal Title: Current Opinion in Hematology
Volume: 25
Issue: 2
ISSN: 1065-6251
Publisher: Lippincott Williams & Wilkins, Ltd.  
Date Published: 2018-03-01
Start Page: 61
End Page: 66
Language: English
DOI: 10.1097/moh.0000000000000405
PROVIDER: scopus
PUBMED: 29278534
PMCID: PMC6601335
DOI/URL:
Notes: Review -- Export Date: 2 April 2018 -- Source: Scopus
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  1. Ross Levine
    776 Levine
  2. Aaron David Viny
    50 Viny