E2a/Pbx1 oncogene inhibits terminal differentiation but not myeloid potential of pro-T cells (Q50724637)

18 March 2018

title

E2a/Pbx1 oncogene inhibits terminal differentiation but not myeloid potential of pro-T cells (English)

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18 March 2018

author name string

Bourette RP

series ordinal

1

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18 March 2018

Grasset MF

series ordinal

2

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18 March 2018

Mouchiroud G

series ordinal

3

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18 March 2018

language of work or name

English

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publication date

3 July 2006

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18 March 2018

published in

Oncogene

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18 March 2018

volume

26

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18 March 2018

issue

2

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18 March 2018

page(s)

234-247

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18 March 2018

Flt3+ macrophage precursors commit sequentially to osteoclasts, dendritic cells and microglia

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PU.1 regulates the commitment of adult hematopoietic progenitors and restricts granulopoiesis

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PU.1 regulates both cytokine-dependent proliferation and differentiation of granulocyte/macrophage progenitors

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MTG8 proto-oncoprotein interacts with the regulatory subunit of type II cyclic AMP-dependent protein kinase in lymphocytes

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AML1-ETO decreases ETO-2 (MTG16) interactions with nuclear receptor corepressor, an effect that impairs granulocyte differentiation

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Enforced granulocyte/macrophage colony-stimulating factor signals do not support lymphopoiesis, but instruct lymphoid to myelomonocytic lineage conversion

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E2A-Pbx1, the t(1;19) translocation protein of human pre-B-cell acute lymphocytic leukemia, causes acute myeloid leukemia in mice

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Redefinition of lymphoid progenitors

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MafB is an inducer of monocytic differentiation

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Lineage infidelity in myeloid cells with TCR gene rearrangement: a latent developmental potential of proT cells revealed by ectopic cytokine receptor signaling

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Runx1 is essential for hematopoietic commitment at the hemangioblast stage of development in vitro

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The Leukemia-associated ETO homologues are differently expressed during hematopoietic differentiation

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Proto-oncogenes of the fos/jun family of transcription factors are positive regulators of myeloid differentiation

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The M-CSF receptor substrate and interacting protein FMIP is governed in its subcellular localization by protein kinase C-mediated phosphorylation, and thereby potentiates M-CSF-mediated differentiation

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Members of the large Maf transcription family regulate insulin gene transcription in islet beta cells

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Dynamic regulation of PU.1 expression in multipotent hematopoietic progenitors

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7 January 2021

Receptor for macrophage colony-stimulating factor transduces a signal decreasing erythroid potential in the multipotent hematopoietic EML cell line

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7 January 2021

ETO/MTG8 is an inhibitor of C/EBPbeta activity and a regulator of early adipogenesis

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Estrogen-dependent E2a/Pbx1 myeloid cell lines exhibit conditional differentiation that can be arrested by other leukemic oncoproteins

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7 January 2021

E2a/Pbx1 induces the rapid proliferation of stem cell factor-dependent murine pro-T cells that cause acute T-lymphoid or myeloid leukemias in mice

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7 January 2021

Transcriptional profiling during the early differentiation of granulocyte and monocyte progenitors controlled by conditional versions of the E2a-Pbx1 oncoprotein

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Transcription factor complex formation and chromatin fine structure alterations at the murine c-fms (CSF-1 receptor) locus during maturation of myeloid precursor cells

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7 January 2021

FMIP, a novel Fms-interacting protein, affects granulocyte/macrophage differentiation

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7 January 2021

Heterogeneity of t(1;19)(q23;p13) acute leukaemias. French Haematological Cytology Group

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7 January 2021

Lack of KIT or FMS internal tandem duplications but co-expression with ligands in AML.

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7 January 2021

FLT3 ligand causes autocrine signaling in acute myeloid leukemia cells

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7 January 2021

Hematopoietic cytokines, transcription factors and lineage commitment

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7 January 2021

Identifiers

DOI

10.1038/SJ.ONC.1209777

1 reference

18 March 2018

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Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/psqn4gtj2jdd3exavh5c3f5bfq

24 November 2022

mapped directly with Wikidata item

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18 March 2018