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Coexistence of LMPP-like and GMP-like leukemia stem cells in acute myeloid leukemia

Authors :
Nicolas Goardon
Paresh Vyas
Alexander Sternberg
Ann Atzberger
David G. Bowen
Mike Griffiths
Steven Knapper
Sally Killick
Suriya Begum
Catherine Porcher
Tariq Enver
Anna Schuh
Andrew Price
Susan Rose
Hannah Hunter
Kate A. Alford
Jamie Cavenagh
Lynn Quek
Amanda F. Gilkes
R Rout
Emanuele Marchi
Elizabeth Macintyre
Alan Kenneth Burnett
Paul Virgo
Sten Eirik W. Jacobsen
Charles Craddock
Shamit Soneji
Graham R. Standen
Nicola Geddes
L. G. Robinson
Petter S. Woll
Salma Chaudhury
Adam J. Mead
Kheira Beldjord
Slama, Catherine
Cytokines, hématopoïèse et réponse immune (CHRI)
Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Université Paris Descartes - Paris 5 (UPD5) - Institut National de la Santé et de la Recherche Médicale (INSERM) - Centre National de la Recherche Scientifique (CNRS)
Source :
Cancer Cell, Cancer Cell; Vol 19, Cancer Cell, Elsevier, 2011, 186, pp.284-290
Publication Year :
2011
Publisher :
HAL CCSD, 2011.

Abstract

SummaryThe relationships between normal and leukemic stem/progenitor cells are unclear. We show that in ∼80% of primary human CD34+ acute myeloid leukemia (AML), two expanded populations with hemopoietic progenitor immunophenotype coexist in most patients. Both populations have leukemic stem cell (LSC) activity and are hierarchically ordered; one LSC population gives rise to the other. Global gene expression profiling shows the LSC populations are molecularly distinct and resemble normal progenitors but not stem cells. The more mature LSC population most closely mirrors normal granulocyte-macrophage progenitors (GMP) and the immature LSC population a previously uncharacterized progenitor functionally similar to lymphoid-primed multipotential progenitors (LMPPs). This suggests that in most cases primary CD34+ AML is a progenitor disease where LSCs acquire abnormal self-renewal potential.

Details

Language :
English
ISSN :
15356108
Database :
OpenAIRE
Journal :
Cancer Cell, Cancer Cell; Vol 19, Cancer Cell, Elsevier, 2011, 186, pp.284-290
Accession number :
edsair.doi.dedup.....5667f3e6f4d6bb89131c3f617009d198