Role of CSF3R mutations in the pathomechanism of congenital neutropenia and secondary acute myeloid leukemia.

Abstract

Acquired mutations in the intracellular part of CSF3R (colony stimulating factor 3 receptor, granulocyte) have been detected with a frequency of more than 30% in severe congenital neutropenia (CN) patients. CN is a preleukemic syndrome with a risk of approximately 20% to develop leukemia. More than 80% of CN patients who develop acute myeloid leukemia or myelodysplastic syndrome reveal CSF3R mutations, suggesting that they are involved in leukemogenesis. Using deep-sequencing technology, we were able to analyze large cohorts of CN patients for the entire CSF3R sequence as well as to identify cell clones carrying mutations in the intracellular part of CSF3R with very high sensitivity. Acquisition of CSF3R mutations is a CN-specific phenomenon and is associated with inherited mutations causing CN or cyclic neutropenia, such as ELANE mutations. In the group of CN patients negative for known germ-line mutations, biallelic CSF3R mutations were identified. In addition, CSF3R mutant clones are highly dynamic and may disappear and reappear during continuous granulocyte colony-stimulating factor (G-CSF) therapy. The time between the first detection of CSF3R mutations and overt leukemia is highly variable.

• Authors: Maksim Klimiankou, Sabine Mellor-Heineke, Cornelia Zeidler, Karl Welte, Julia Skokowa
• Journal: Annals of the New York Academy of Sciences (Ann N Y Acad Sci) Vol. 1370 Issue 1 Pg. 119-25 (04 2016) ISSN: 1749-6632 [Electronic] United States
• PMID: 27270496 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2016 New York Academy of Sciences.

Chemical References

• CSF3R protein, human
• Receptors, Colony-Stimulating Factor

Topics

• High-Throughput Nucleotide Sequencing
• Humans
• Leukemia, Myeloid, Acute (etiology, genetics, metabolism)
• Mutation
• Neutropenia (complications, congenital, genetics, metabolism)
• Receptors, Colony-Stimulating Factor (genetics, metabolism)