Notch1 signaling promotes human t-cell acute lymphoblastic leukemia initiating cell regeneration in supportive niches

Wenxue Ma, Alejandro Gutierrez, Daniel J. Goff, Ifat Geron, Anil Sadarangani, Christina A.M. Jamieson, Angela C. Court, Alice Y. Shih, Qingfei Jiang, Christina C. Wu, Kang Li, Kristen M. Smith, Leslie A. Crews, Neil W. Gibson, Ida Deichaite, Sheldon R. Morris, Ping Wei, Dennis A. Carson, A. Thomas Look, Catriona H.M. Jamieson

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32 Citas (Scopus)


Background: Leukemia initiating cells (LIC) contribute to therapeutic resistance through acquisition of mutations in signaling pathways, such as NOTCH1, that promote self-renewal and survival within supportive niches. Activating mutations in NOTCH1 occur commonly in T cell acute lymphoblastic leukemia (T-ALL) and have been implicated in therapeutic resistance. However, the cell type and context specific consequences of NOTCH1 activation, its role in human LIC regeneration, and sensitivity to NOTCH1 inhibition in hematopoietic microenvironments had not been elucidated. Methodology and Principal Findings: We established humanized bioluminescent T-ALL LIC mouse models transplanted with pediatric T-ALL samples that were sequenced for NOTCH1 and other common T-ALL mutations. In this study, CD34+ cells from NOTCH1Mutated T-ALL samples had higher leukemic engraftment and serial transplantation capacity than NOTCH1Wild-type CD34+ cells in hematopoietic niches, suggesting that self-renewing LIC were enriched within the NOTCH1Mutated CD34+ fraction. Humanized NOTCH1 monoclonal antibody treatment reduced LIC survival and self-renewal in NOTCH1Mutated T-ALL LIC-engrafted mice and resulted in depletion of CD34+CD2+CD7+ cells that harbor serial transplantation capacity. Conclusions: These results reveal a functional hierarchy within the LIC population based on NOTCH1 activation, which renders LIC susceptible to targeted NOTCH1 inhibition and highlights the utility of NOTCH1 antibody targeting as a key component of malignant stem cell eradication strategies.
Idioma originalInglés
Número de artículoe39725
PublicaciónPLoS ONE
EstadoPublicada - 29 jun. 2012
Publicado de forma externa

Nota bibliográfica

© Copyright 2013 Elsevier B.V., All rights reserved. © MEDLINE® is the source for the MeSH terms of this document.

Palabras clave

  • Adolescent
  • Animals
  • Antibodies
  • Monoclonal
  • Cell proliferation
  • Cell survival
  • Child
  • Preschooler
  • Humans
  • Mice
  • Mutation
  • Neoplasm transplantation
  • Neoplastic stem cells
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
  • Receptor
  • Notch1
  • Regeneration
  • Signal Transduction
  • Stem Cell Niche
  • Young adult


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