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CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition
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 li...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410536/ https://www.ncbi.nlm.nih.gov/pubmed/33960108 http://dx.doi.org/10.1002/1878-0261.12982 |
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author | Galland, Ava Gourain, Victor Habbas, Karima Güler, Yonca Martin, Elisabeth Ebel, Claudine Tavian, Manuela Vallat, Laurent Chenard, Marie‐Pierre Mauvieux, Laurent Freund, Jean‐Noël Duluc, Isabelle Domon‐Dell, Claire |
author_facet | Galland, Ava Gourain, Victor Habbas, Karima Güler, Yonca Martin, Elisabeth Ebel, Claudine Tavian, Manuela Vallat, Laurent Chenard, Marie‐Pierre Mauvieux, Laurent Freund, Jean‐Noël Duluc, Isabelle Domon‐Dell, Claire |
author_sort | Galland, Ava |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8410536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84105362021-09-03 CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition Galland, Ava Gourain, Victor Habbas, Karima Güler, Yonca Martin, Elisabeth Ebel, Claudine Tavian, Manuela Vallat, Laurent Chenard, Marie‐Pierre Mauvieux, Laurent Freund, Jean‐Noël Duluc, Isabelle Domon‐Dell, Claire Mol Oncol Research Articles 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. John Wiley and Sons Inc. 2021-06-26 2021-09 /pmc/articles/PMC8410536/ /pubmed/33960108 http://dx.doi.org/10.1002/1878-0261.12982 Text en © 2021 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Galland, Ava Gourain, Victor Habbas, Karima Güler, Yonca Martin, Elisabeth Ebel, Claudine Tavian, Manuela Vallat, Laurent Chenard, Marie‐Pierre Mauvieux, Laurent Freund, Jean‐Noël Duluc, Isabelle Domon‐Dell, Claire CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition |
title | CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition |
title_full | CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition |
title_fullStr | CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition |
title_full_unstemmed | CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition |
title_short | CDX2 expression in the hematopoietic lineage promotes leukemogenesis via TGFβ inhibition |
title_sort | cdx2 expression in the hematopoietic lineage promotes leukemogenesis via tgfβ inhibition |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8410536/ https://www.ncbi.nlm.nih.gov/pubmed/33960108 http://dx.doi.org/10.1002/1878-0261.12982 |
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