A stemness screen reveals as a promoter of human leukemia stem cell latency.

Blood 2019 05 22;133(20):2198-2211. Epub 2019 Feb 22.

Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.

There is a growing body of evidence that the molecular properties of leukemia stem cells (LSCs) are associated with clinical outcomes in acute myeloid leukemia (AML), and LSCs have been linked to therapy failure and relapse. Thus, a better understanding of the molecular mechanisms that contribute to the persistence and regenerative potential of LSCs is expected to result in the development of more effective therapies. We therefore interrogated functionally validated data sets of LSC-specific genes together with their known protein interactors and selected 64 candidates for a competitive in vivo gain-of-function screen to identify genes that enhanced stemness in human cord blood hematopoietic stem and progenitor cells. A consistent effect observed for the top hits was the ability to restrain early repopulation kinetics while preserving regenerative potential. Overexpression (OE) of the most promising candidate, the orphan gene , in a patient-derived AML model (8227) promoted the retention of LSCs in a primitive state manifested by relative expansion of CD34 cells, accumulation of cells in G, and reduced output of differentiated progeny. Despite delayed early repopulation, at later times, -OE resulted in the expansion of self-renewing LSCs. In contrast, silencing in primary AML reduced regenerative potential. Mechanistically, our multidimensional confocal analysis found that regulates G exit by interfering with nuclear localization of its target PAK4, with concomitant reduction of global H4K16ac levels. These data identify as a novel regulator of LSC latency and reveal a link between the regulation of stem cell kinetics and pool size during regeneration.

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http://dx.doi.org/10.1182/blood-2018-10-881441DOI Listing
May 2019
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