CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition.
Ava GallandVictor GourainKarima HabbasYonca GülerElisabeth MartinClaudine EbelManuela TavianLaurent VallatMarie-Pierre ChenardLaurent MauvieuxJean-Noël FreundIsabelle DulucClaire Domon-DellPublished in: Molecular oncology (2021)
The intestine-specific caudal-related homeobox gene-2 (CDX2) homeobox gene, while being a tumor suppressor in the gut, is ectopically expressed in a large proportion of acute leukemia and is associated with poor prognosis. Here, we report that turning on human CDX2 expression in the hematopoietic lineage of mice induces acute monoblastic leukemia, characterized by the decrease in erythroid and lymphoid cells at the benefit of immature monocytic and granulocytic cells. One of the highly stimulated genes in leukemic bone marrow cells was BMP and activin membrane-bound inhibitor (Bambi), an inhibitor of transforming growth factor-β (TGF-β) signaling. The CDX2 protein was shown to bind to and activate the transcription of the human BAMBI promoter. Moreover, in a leukemic cell line established from CDX2-expressing mice, reducing the levels of CDX2 or Bambi stimulated the TGF-β-dependent expression of Cd11b, a marker of monocyte maturation. Taken together, this work demonstrates the strong oncogenic potential of the homeobox gene CDX2 in the hematopoietic lineage, in contrast with its physiological tumor suppressor activity exerted in the gut. It also reveals, through BAMBI and TGF-β signaling, the involvement of CDX2 in the perturbation of the interactions between leukemia cells and their microenvironment.
Keyphrases
- poor prognosis
- transforming growth factor
- bone marrow
- induced apoptosis
- cell cycle arrest
- long non coding rna
- acute myeloid leukemia
- endothelial cells
- mesenchymal stem cells
- genome wide
- epithelial mesenchymal transition
- copy number
- transcription factor
- type diabetes
- dna methylation
- stem cells
- cell death
- binding protein
- signaling pathway
- magnetic resonance imaging
- intensive care unit
- dendritic cells
- gene expression
- genome wide identification
- oxidative stress
- small molecule
- adipose tissue
- insulin resistance
- high fat diet induced