Transplantable cell lines generated with NUP98-Hox fusion genes undergo leukemic progression by Meis1 independent of its binding to DNA (Q81471229)

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9 January 2020

title

Transplantable cell lines generated with NUP98-Hox fusion genes undergo leukemic progression by Meis1 independent of its binding to DNA (English)

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9 January 2020

3

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author name string

Pineault N

series ordinal

1

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9 January 2020

Abramovich C

series ordinal

2

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9 January 2020

publication date

1 April 2005

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9 January 2020

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9 January 2020

volume

19

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issue

4

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9 January 2020

page(s)

636-643

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2403696

9 January 2020

exact match

0 references

cites work

HOX and non-HOX homeobox genes in leukemic hematopoiesis

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NUP98 gene fusions in hematologic malignancies.

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Differential and common leukemogenic potentials of multiple NUP98-Hox fusion proteins alone or with Meis1

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Overexpression of HOXB3 in hematopoietic cells causes defective lymphoid development and progressive myeloproliferation

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NUP98-HOXA9 expression in hemopoietic stem cells induces chronic and acute myeloid leukemias in mice

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Induction of acute myeloid leukemia in mice by the human leukemia-specific fusion gene NUP98-HOXD13 in concert with Meis1

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Molecular mechanisms of leukemogenesis mediated by MLL fusion proteins

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Defining roles for HOX and MEIS1 genes in induction of acute myeloid leukemia

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Differential expression of Hox, Meis1, and Pbx1 genes in primitive cells throughout murine hematopoietic ontogeny

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Hematopoietic, angiogenic and eye defects in Meis1 mutant animals

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Inhibition of myeloid differentiation by Hoxa9, Hoxb8, and Meis homeobox genes

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Meis1a suppresses differentiation by G-CSF and promotes proliferation by SCF: potential mechanisms of cooperativity with Hoxa9 in myeloid leukemia

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Nup98-HoxA9 immortalizes myeloid progenitors, enforces expression of Hoxa9, Hoxa7 and Meis1, and alters cytokine-specific responses in a manner similar to that induced by retroviral co-expression of Hoxa9 and Meis1

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7 January 2021

Hoxa9 immortalizes a granulocyte-macrophage colony-stimulating factor-dependent promyelocyte capable of biphenotypic differentiation to neutrophils or macrophages, independent of enforced meis expression

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HoxB8 requires its Pbx-interaction motif to block differentiation of primary myeloid progenitors and of most cell line models of myeloid differentiation

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7 January 2021

PBX and MEIS as non-DNA-binding partners in trimeric complexes with HOX proteins

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7 January 2021

Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b

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7 January 2021

Establishment of a pluripotent preleukaemic stem cell line by expression of the AML1-ETO fusion protein in Notch1-immortalized HSCN1cl10 cells

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7 January 2021

Meis1, a PBX1-related homeobox gene involved in myeloid leukemia in BXH-2 mice

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7 January 2021

Expression of HOX genes, HOX cofactors, and MLL in phenotypically and functionally defined subpopulations of leukemic and normal human hematopoietic cells

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7 January 2021

Therapeutic implications of cancer stem cells.

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7 January 2021

AbdB-like Hox proteins stabilize DNA binding by the Meis1 homeodomain proteins

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7 January 2021

HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells

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7 January 2021